Ewart Ray Herbert Jones
Bibliography
Jones 1
Ewart Ray Herbert Jones—Bibliography
Scientific papers and reviews
Titles are as rendered by SciFinder Scholar®, corrected in a few cases for gross errors: editorial adjustments introduced
by Chemical Abstracts have not been reversed. Within each year group, papers are ordered arbitrarily.
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1934
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1935
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1936
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1937
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1938
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1939
1940
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1941
1942
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1943
(With A. E. Bradfield, J. L. Simonsen) Syntheses in the sesquiterpene series. I; J. Chem. Soc., 18101812.
(With A. E. Bradfield, J. L. Simonsen) Syntheses in the sesquiterpene series. II. Condensation of ethyl
oxalate and tetrahydrocarvone; J. Chem. Soc., 315-317.
(With A. E. Bradfield, J. L. Simonsen) Syntheses in the sesquiterpene series. III. A synthesis of 1:10dimethyl-7-isopropyldecal-2-one; J. Chem. Soc., 1137-1143.
(With F. S. Spring) Studies in the sterol group. XXVIII. Application of the Reformatsky reaction to
7-ketocholesteryl acetate: 5-cholestene-3:7-diol-7-acetic acid; J. Chem. Soc., 302-304.
(With I. M. Heilbron, F. S. Spring) Studies in the sterol group. XXXII. The bromination of 6ketocholestanyl acetate; J. Chem. Soc., 801-805.
(With I. M. Heilbron, H. Jackson, F. S. Spring) Studies in the sterol group. XXXIV. Dibromination
of 6-ketocholestanyl acetate; J. Chem. Soc., 102-107.
(With T. Barr, I. M. Heilbron, F. S. Spring) Studies in the sterol group. XXXV. The bromination of 7ketocholestanyl acetate; J. Chem. Soc., 334-337.
(With H. Jackson) Studies in the sterol group. XXXVIII. Bromination of 6-keto-3-acetoxy-4cholestene; J. Chem. Soc., 1406-1408.
Caoutchicol; Chem. and Ind., 446.
(With J. Barnett, I. M. Heilbron, K. J. Verrill) Studies in the sterol group. XLI. A new epimerization
process; J. Chem. Soc., 1390-1393.
(With L. C. Cross) Constituents of the higher fungi. II. The unsaturated system of polyporenic acid A;
J. Chem. Soc., 1491-1493.
(With L. C. Cross, C. G. Eliot, I. M. Heilbron) Constituents of the higher fungi. I. The triterpene acids
of Polyporus betulinus Fr; J. Chem. Soc., 632-636.
(With B. Heath-Brown, I. M. Heilbron) Studies in the sterol group. XLII. The constitution of
zymosterol; J. Chem. Soc., 1482-1489.
(With I. M. Heilbron) The chemistry of the sterols; Ann. Rev. Biochem., 11, 135-172.
(With H. Jackson) Studies in the sterol group. XL. The bromination of 7-ketocholesteryl acetate; J.
Chem. Soc., 659-663.
Carotenoids; Ann. Repts. Progress Chem. (Chem. Soc. London), 37, 290-312.
(With K. J. Verrill) Enol acetate in the triterpene series; J. Chem. Soc., 1512.
(With R. J. Meakins) Oxidation of lupenyl esters; J. Chem. Soc., 1335-1339.
(With R. J. Meakins) Lupanetriol and its oxidation; J. Chem. Soc., 456-457.
(With P. Bilham, R. J. Meakins) Surface films of lupane derivatives; J. Chem. Soc., 761-766.
(With I. M. Heilbron, K. C. Roberts, P. A. Wilkinson) Studies in the sterol group. XLIII. The
unsaponifiable portion of the acetone extract of plantation rubber; J. Chem. Soc., 344-347.
Synthetic polyenes; Ann. Repts. Progress Chem. (Chem. Soc. London), 38, 170-187.
(With R. J. Meakins) Constitution of lupeol; J. Chem. Soc., 757-761.
(With I. M. Heilbron, A. W. Johnson, A. Spinks (Polyene series. V. The employment of 3-(2':6':6'trimethylcyclohexenyl-l-methylcrotonaldehyde) for the synthesis of vitamin A and analogues; J.
Chem. Soc., 727-733.
(With I. M. Heilbron, H. P. Koch) Polyene series. VII. Carbinols from propargyl acetal
[propiolaldehyde diethyl acetal]; J. Chem. Soc., 735-737.
(With H. P. Koch) Self-condensation of acetylcyclohexene; J. Chem. Soc., 393-395.
(With J. T. McCombie) Polyene series. VI. The preparation of ethinyl carbinols from ,-unsaturated
aldehydes; J. Chem. Soc., 733-735.
(With P. A. Wilkinson, R. H. Kerlogue) Studies in the sterol group. XLIV. The oxidation of
phytosterols with the Oppenauer reagent; J. Chem. Soc., 391-393
(With D. H. R. Barton) Studies in the sterol group. XLVI. Isolation of a new form of 4-cholestenone;
J. Chem. Soc., 602-603.
(With D. H. R. Barton) Studies in the sterol group. XLV. Investigation of the homogeneity of
sitosterol by oxidation with the Oppenauer reagent; J. Chem. Soc., 599-602.
(With I. M. Heilbron, R. A. Raphael) Polyene series. XI. The anionotropic rearrangement of the
acetylenic glycol from crotonaldehyde; J. Chem. Soc., 268-270.
(With I. M. Heilbron, A. W. Johnson, R. A. Raphael) Polyene series. X. Condensation of 3-methyl-2penten-4-yne (1,2-dimethylvinylacetylene) with butaldehyde, crotonaldehyde and citral. Anionotropic
rearrangements with vinylacetylenecarbinols derived from ,-unsaturated aldehydes; J. Chem. Soc.,
265-268.
Jones 2
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1944
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1945
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1946
(With I. M. Heilbron, R. A. Raphael) Polyene series. IX. The condensation product of 1-hexyne with
crotonaldehyde and its anionotropic rearrangement; J. Chem. Soc., 264-265.
Steroid syntheses; Ann. Repts. Progress Chem. (Chem. Soc. London), 40, 122-147.
(With H. T. Openshaw, L. N. Owen, F. S. Spring) Organic chemistry. Introduction; Ann. Repts.
Progress Chem. (Chem. Soc. London), 40, 98-100.
Attempts to synthesize vitamin A; Sci. J. Roy. Coll. Sci., 13, 19-26.
Recent advances in organic chemical methods; Nature, 151, 564.
(With J. T. McCombie) Polyene series. VIII. A new anionotropic rearrangement. Isomerization of
ethynylcarbinols from ,-unsaturated aldehydes; J. Chem. Soc., 261-264.
(With D. H. R. Barton) Optical rotatory power and structure in triterpenoid compounds. Application
of the method of molecular rotation differences; J. Chem. Soc., 659-665.
(With E. A. Braude) Kinetics of anionotropic rearrangement. I. Rearrangement of
propenylethynylcarbinol; J. Chem. Soc., 436-443.
(With J. Cymerman, I. M. Heilbron) Polyene series. XVI. The condensation of ,-unsaturated
ketones with 1-hexyne; J. Chem. Soc., 144-147.
(With J. Cymerman, I. M. Heilbron, A. W. Johnson) Polyene series. XV. The condensation of
carbonyl compounds with propenylethynylcarbinol and 3-hexen-5-yn-2-ol; J. Chem. Soc., 141-144.
(With I. M. Heilbron, B. C. L. Weedon) Polyene series. XIV. Anionotropic rearrangements of the
carbinols obtained from condensation of crotonaldehyde with both vinyl- and 2-methylvinylacetylene;
J. Chem. Soc., 140-141.
(With I. M. Heilbron, R. A. Raphael) Polyene series. XIII. Acetylenyl glycols from polyene
aldehydes and their rearrangement with acids; J. Chem. Soc., 136-139.
(With I. M. Heilbron, J. T. McCombie) Polyene series. XII. Ethynylcarbinols form sorbaldehyde and
octatrienal. Polycarbon anionotropic, rearrangements; J. Chem. Soc., 134-136.
(With E. A. Braude) Light absorption. II. 2,4-Dinitrophenylhydrazones; J. Chem. Soc., 498-503.
(With A. G. Caldwell) Constituents of expressed West Indian lime oil; J. Chem. Soc., 540-543.
(With J. Cymerman, I. M. Heilbron) Polyene series. XXI. Ethynylcarbinols from ,-unsaturated
ketones: their anionotropic rearrangements and other reactions; J. Chem. Soc., 90-94.
(With L. J. Haynes) Synthesis of the differential growth inhibitor, -hexenolactone; Nature, 155, 730.
(With I. M. Heilbron, J. T. McCombie, B. C. L. Weedon) Polyene series. XX. Formation of ethers
and esters from propenylvinylcarbinol and related compounds and the simultaneous rearrangements;
J. Chem. Soc., 88-90.
(With I. M. Heilbron, J. T. McCombie, B. C. L. Weedon) Polyene series. XIX. Semihydrogenation of
ethynylcarbinols derived from ,-unsaturated aldehydes and the anionotropic rearrangements of the
resulting vinylcarbinols; J. Chem. Soc., 84-87.
(With I. M. Heilbron, B. C. L. Weedon) Polyene series. XVIII. Formation of ethers from
propenylethynylcarbinol and related compounds; J. Chem. Soc., 81-84.
(With I. M. Heilbron, R. N. Lacey, J. T. McCombie, R. Raphael) Polyene series. XVII. Replacement
halogenation and simultaneous anionotropic rearrangements of acetylenylcarbinols and glycols
derived from ,-unsaturated aldehydes; J. Chem. Soc., 77-81.
Acetylenic compounds; Ann. Repts. Progress Chem. (Chem. Soc. London), 41, 148-181.
(With K. Bowden, E. A. Braude) Light absorption. III. Auxochromic properties and the periodic
system; J. Chem. Soc., 948-952.
(With K. Bowden) Acetylenic compounds. IX. Heterocyclic compounds derived from ethynyl
ketones; J. Chem. Soc., 953-954.
(With K. Bowden, E. A. Braude) Acetylenic compounds. VIII. Miscellaneous addition reactions of
ethynyl ketones; J. Chem. Soc., 945-948.
(With K. Bowden) Acetylenic compounds. III. Diene additions to ethynyl ketones; J. Chem. Soc., 5254.
(With K. Bowden, E. A. A. Braude, B. C. L. Weedon) Acetylenic compounds. II. The addition of
amines to ethynyl ketones. Auxochromic properties and conjugating power of the amino group; J.
Chem. Soc., 45-52.
(With K. Bowden, I. M. Heilbron, B. C. L. Weedon) Acetylenic compounds. I. Preparation of
acetylenic ketones by oxidation of acetylenic carbinols and glycols; J. Chem. Soc., 39-45.
(With E. A. Braude, E. S. Stern) Kinetics of anionotropic rearrangement. V. Oxotropic formation of
the styrene system; J. Chem. Soc., 396-404.
(With E. A. Braude) Kinetics of anionotropic rearrangement. IV. Substituent effects in the oxotropic
formation of the butadiene system. Comparison of the electron-attracting properties of the ethylenic
and acetylenic bonds; J. Chem. Soc., 128-130.
(With E. A. Braude) Kinetics of anionotropic rearrangement. III. Substituent effects in the oxotropic
formation of the vinylacetylene system; J. Chem. Soc., 123-127.
(With A. G. Caldwell) Preparation and bacteriostatic properties of some amines derived from citral; J.
Chem Soc., 597-599.
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1947
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1948
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1949
(With A. G. Caldwell) Rearrangement of aldoximes into amides with Raney nickel. Stereoisomeric
geranamides; J. Chem. Soc., 599-601.
(With J. Cymerman, I. M. Heilbron, R. N. Lacey) Polyene series. XXIII. Condensation of the C14
aldehyde [3-(2',6',6'-trimethylcyclohexenyl)-1-methylcrotonaldehyde] with 1-hexyne and 2methoxyhex-3-en-5-yne; J. Chem. Soc., 500-503.
(With L. J. Haynes) Acetylenic compounds. X. Unsaturated lactones. Part I. A new route to growthinhibitory ,-ethylenic - and -lactones; J. Chem. Soc., 954-957.
(With L. J. Haynes) Acetylenic compounds. V. ,-Acetylenic hydroxy acids; J. Chem. Soc., 503506.
(With I. M. Heilbron, D. G. O'Sullivan) Polyene series. XXIV. The C17 acid and C18 ketone related to
vitamin A; J. Chem. Soc., 866-869.
(With I. M. Heilbron, D. G. O'Sullivan) Substances related to vitamin A; Nature, 157, 485-486.
(With I. M. Heilbron, P. Smith, B. C. L. Weedon) Acetylenic compounds. IV. The hydration of some
acetylenylcarbinols derived from ,-unsaturated aldehydes; J. Chem. Soc., 54-58.
(With I. M. Heilbron, R. N. Lacey) Polyene series. XXII. Condensations between methyl propargyl
ether and ,-unsaturated carbonyl compounds; J. Chem. Soc., 27-30.
(With H. B. Henbest) Etherifications accompanying Girard treatment for the separation of ketonic
substances; Nature, 158, 950.
(With H. B. Henbest, A. E. Bide, R. W. Peevers, P. A. Wilkinson) A new route to 7dehydrocholesterol, provitamin D3; Nature, 158, 169.
(With R. N. Lacey, P. Smith) Acetylenic compounds. VII. Reactions of 2-chlorohex-3-en-5-yne and
related compounds with ammonia and amines. Reversed anionotropic rearrangements accompanying
replacement; J. Chem. Soc., 940-944.
(With B. C. L. Weedon) Acetylenic compounds. VI. Carbinols derived from methyl -chlorovinyl
ketone and their conversion into unsaturated aldehydes; J. Chem. Soc., 937-939.
(With F. A. Robinson, M. N. Strachan) 5-Spirothiazolidiones; J. Chem. Soc., 91-92.
(With F. A. Robinson, M. N. Strachan) Aminoalkyl esters of thiazolecarboxylic and thiazolyl-4-acetic
acid; J. Chem. Soc., 87-91.
(With K. Bowden, I. M. Heilbron, K. H. Sargent) Acetylenic compounds. XII. The preparation of
conjugated diacetylenic glycols by the oxidative coupling of various types of ethynylcarbinols; J.
Chem. Soc., 1579-1583.
(With E. A. Braude, E. S. Stern) Preparation and ultraviolet light absorption of some substituted
phenylpropenyl- and styrylmethylcarbinols and 1-phenylbutadienes; J. Chem. Soc., 1087-1096.
(With E. A. Braude, G. G. Rose) Light absorption. IV. Nitro-olefins; J. Chem. Soc., 1104-1105.
(With L. J. Haynes, I. M. Heilbron, F. Sondheimer) Acetylenic compounds. XIII. The reaction
between epichlorohydrin and sodium acetylide. A novel route to the ethynyl-ethylenic alcohol, 2penten-4-yn-1-ol; J. Chem. Soc., 1583-1585.
(With I. M. Heilbron, F. Sondheimer) Acetylenic compounds. XIV. The reactions of the readily
available ethynyl-ethylenic alcohol, 2-penten-4-yn-1-ol; J. Chem. Soc., 1586-1590.
(With I. Marszak, H. Bader) Acetylenic compounds. XI. The Mannich reaction with monosubstituted
acetylenic compounds; J. Chem. Soc., 1578-1579.
(With A. E. Bide, H. B. Henbest, P. A. Wilkinson) Studies in the sterol group. XLVIII. 7-Substituted
cholesterol derivatives and their stereochemistry. Part I. 7-Halo derivatives; J. Chem. Soc., 17881792.
(With A. E. Bide, H. B. Henbest, R. W. Peevers, P. A. Wilkinson) Studies in the sterol group. XLVII.
New route to 7-dehydrocholesterol (provitamin D3) and its derivatives; J. Chem. Soc., 1783-1788.
(With P. W. Carter, L. C. Cross, I. M. Heilbron) The algae. IV. Lipochromes of the male and female
gametes of some species of the Fucaceae; Biochem. J., 43, 349-352.
(With J. R. Catch, D. F. Elliott, D. H. Hey) Halogenated ketones. IV. The application of the FriedelCrafts reaction to the preparation of halogenated aliphatic ketones; J. Chem. Soc., 278-281.
(With J. R. Catch, D. F. Elliott, D. H. Hey) Halogenated ketones. III. The preparation of bromomethyl
ketones by the diazo reaction; J. Chem. Soc., 278.
(With J. R. Catch, D. H. Hey, W. Wilson) Halogenated ketones. II. The bromination of methyl propyl
and methyl isopropyl ketone; J. Chem. Soc., 276-277.
(With J. R. Catch, D. F. Elliott, D. H. Hey) Halogenated ketones. I. The bromination of acetone and
methyl ethyl ketone; J. Chem. Soc., 272-275.
(With H. B. Henbest) Studies in the sterol group. L. 7-Substituted cholesterol derivatives and their
stereochemistry. Part III. 7-Alkoxycholesterol derivatives; J. Chem. Soc., 1798-1803.
(With H. B. Henbest) Studies in the sterol group. XLIX. 7-Substituted cholesterol derivatives and
their stereochemistry. Part II. Esters of the epimeric 7-hydroxycholesterols; J. Chem. Soc., 17921797.
(With T. R. Ames) Structure of the triterpenes-an interrelation between the lupeol and the -amyrin
series; Nature, 164, 1090-1091.
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1950
(With H. Bader, L. C. Cross, I. M. Heilbron) Acetylenic compounds. XVIII. The addition of
thiolacetic acid to acetylenic hydrocarbons. The conversion of monosubstituted acetylenes into
aldehydes and 1,2-dithiols; J. Chem. Soc., 619-623.
(With E. A. Braude, H. P. Koch, R. W. Richardson, F. Sondheimer, J. B. Toogood) Light absorption.
VI. Steric inhibition of resonance in natural and synthetic derivatives of cyclohexene; J. Chem. Soc.,
1890-1897.
(With E. A. Braude, F. Sondheimer, J. B. Toogood) Acetylenic compounds. XVI. The preparation,
reactions, and light-absorption properties of some 2,5-dihydroacetophenones and related compounds.
(Light absorption Part V); J. Chem. Soc., 607-614.
(With J. R. Catch, D. F. Elliott, D. H. Hey) Halogenated ketones. V. Some derivatives of chloroacetophenone; J. Chem. Soc., 552-555.
(With G. W. H. Cheeseman, I. M. Heilbron, B. C. L. Weedon) Polyene series. XXXIV. The synthesis
of a C17 alcohol related to vitamin A; J. Chem. Soc., 3120-3123.
(With G. W. H. Cheeseman, I. M. Heilbron, F. Sondheimer, B. C. L. Weedon, M. Julia) Polyene
series. XXXIII. The preparation of 6-methyl-3,5,7-octatrien-2-one, a key intermediate for the
synthesis of vitamin A and its analogs; J. Chem. Soc., 2031-2035.
(With G. W. H. Cheeseman, I. M. Heilbron, F. Sondheimer, B. C. L. Weedon) Polyene series.
XXVIII. The structure of the C14 aldehyde derived from -ionone and its use for the synthesis of
norvitamin A and isovitamin A derivatives; J. Chem. Soc., 1516-1524.
(With I. M. Heilbron, J. B. Toogood, B. C. L. Weedon) Polyene series. XXXII. Further syntheses of
analogs of -ionone; J. Chem. Soc., 2028-2030.
(With I. M. Heilbron, D. G. Lewis, B. C. L. Weedon) Polyene series. XXXI. The synthesis of C18 and
C19 acids related to vitamin A; J. Chem. Soc., 2023-2027.
(With I. M. Heilbron, M. Julia) Acetylenic compounds. XX. Some reactions of the acetylenicethylenic aldehyde, 3-methyl-2-penten-4-yn-1-al; J. Chem. Soc., 1430-1434.
(With I. M. Heilbron, J. B. Toogood, B. C. L. Weedon) Polyene series. XXX. The synthesis of
cyclopentenyl and cycloheptenyl analogs of -ionone; J. Chem. Soc., 1827-1830.
(With I. M. Heilbron, M. Julia, B. C. L. Weedon) Polyene series. XXIX. Ethoxyacetylenic carbinols
and their conversion into ,-unsaturated aldehydes and acids; J. Chem. Soc., 1823-1827.
(With I. M. Heilbron, D. G. Lewis, R. W. Richardson, B. C. L. Weedon) Polyene series. XXVII. The
synthesis of a biologically active C16 acid; J. Chem. Soc., 742-746.
(With I. M. Heilbron, R. W. Richardson, F. Sondheimer) Polyene series. XXVI. The synthesis of
analogs of -ionone; J. Chem. Soc., 737-741.
(With I. M. Heilbron, P. A. Robins) Nonsaponifiable matter of shea-nut fat. IV. A new tetracyclic
diethenoid alcohol, butyrospermol; J. Chem. Soc., 444-449.
(With I. M. Heilbron, R. W. Richardson) Polyene series. XXV. Molecular structure and vitamin A
activity. Synthesis of a biologically active C17 acid; J. Chem. Soc., 287-293.
(With I. M. Heilbron, F. Sondheimer) Acetylenic compounds. XV. The oxidation of primary
acetylenic carbinols and glycols; J. Chem. Soc., 604-607.
(With H. B. Henbest, I. M. S. Walls) Acetylenic compounds. XXI. Reformatsky reactions with
propargyl bromides; J. Chem. Soc., 2696-2700.
(With M. C. Whiting) Unsaturated lactones. III. Compounds related to auxin-a and auxin-b. I; J.
Chem. Soc., 1419-1423.
(With M. C. Whiting) Unsaturated lactones. II. Acetylenic compounds. XIX. Reactions of the esters
of ,-acetylenic hydroxy acids with nucleophilic reagents; J. Chem. Soc., 1423-1430.
(With D. G. O'Sullivan, M. C. Whiting) Reformatsky reactions with methyl -bromocrotonate; J.
Chem. Soc., 1415-1418.
(With W. Wilson) Preparation of some chloroalkylamino compounds; J. Chem. Soc., 547-552.
(With F. Sondheimer) Acetylenic compounds. XVII. The preparation of substituted 1acetylcyclohexenes from 4-benzoyloxycyclohexanone; J. Chem. Soc., 615-618.
(With E. A. Braude) Structure and light absorption of methylionones; J. Am. Chem. Soc., 72, 10411042.
(With J. B. Brown, H. B. Henbest) Compounds related to auxin a and auxin b. III. The preparation
and properties of the cyclopentenyl analogs of auxin b lactone; J. Chem. Soc., 3634-3641.
(With G. S. Davy, T. G. Halsall) Chemistry of the pentacyclic triterpenes: elucidation of the betulinoleanolic acid relationship; Chem. and Ind., 732.
(With G. S. Davy, T. G. Halsall) Degradation of lupeol derivatives to C27-ketones; Rec. trav. chim.,
69, 368-372.
(With H. B. Henbest) Compounds related to auxin a and auxin b. II. Preparation of analogs of auxin b
lactone; J. Chem. Soc., 3628-3633.
(With H. B. Henbest, I. M. S. Walls) Acetylenic compounds. XXVI. Further Reformatsky reactions
with propargyl bromides; J. Chem. Soc., 3646-3650.
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1952
(With T. Y. Shen, M. C. Whiting) Acetylenic compounds. XXIII. The preparation and properties of
,-acetylenic -keto esters; J. Chem. Soc., 236-241.
(With T. Y. Shen, M. C. Whiting) Acetylenic compounds. XXII. The reaction between nickel
carbonyl and monosubstituted acetylenic compounds; J. Chem. Soc., 230-236.
Acetylene and acetylenic compounds in organic synthesis; J. Chem. Soc., 754-761.
(With T. R. Ames, G. S. Davy, T. G. Halsall, G. D. Meakins) The chemistry of the pentacyclic
triterpenes; the formation of 18-iso--amyranol and germanicol from lupeol; Chem. and Ind., 741.
(With T. R. Ames, T. G. Halsall) Chemistry of the triterpenes. VII. An interrelationship between the
lupeol and the -amyrin series. Elucidation of the structure of lupeol; J. Chem. Soc., 450-457.
(With T. R. Ames, G. S. Davy, T. G. Halsall) The chloro- and iodoacetates of -amyrin, -amyrin,
and lupeol; J. Chem. Soc., 2506-2507.
(With J. B. Armitage, M. C. Whiting) Acetylenic compounds. XXVIII. A new route to diacetylene
and its symmetrical derivatives; J. Chem. Soc., 44-47.
(With G. S. Davy, T. G. Halsall, G. D. Meakins) Chemistry of the triterpenes. X. The structures of
some isomerization products from betulin and betulinic acid; J. Chem. Soc., 2702-2705.
(With G. S. Davy, T. G. Halsall) Chemistry of the triterpenes. IX. Elucidation of the betulin-oleanolic
acid relationship; J. Chem. Soc., 2696-2702.
(With G. S. Davy, T. G. Halsall) Chemistry of the triterpenes. VIII. The - and -amyrenes; J. Chem.
Soc., 458-461.
(With G. S. Davy, T. G. Halsall) The chemistry of the pentacyclic triterpenes: The stereo-chemistry of
rings D and E of the lupeol group; Chem. and Ind., 233.
(With K. R. Farrar, J. C. Hamlet, H. B. Henbest) Elucidation of the structure of vitamin A 2 by total
synthesis; Chem. and Ind., 49-50.
(With C. W. Greenhalgh, H. B. Henbest) Studies in the sterol group. LI. Reactions between 17-keto
steroids and organometallic compounds; J. Chem. Soc., 1190-1193.
(With J. C. Hamlet, H. B. Henbest) Acetylenic compounds. XXXII. Dehydration of acetylphenyl and
vinylacetylenyl alcohols derived from cyclohexanone and the hydration of the resultant hydrocarbons;
J. Chem. Soc., 2652-2659.
(With M. C. Whiting, J. B. Armitage, C. L. Cook, N. Entwistle) Synthesis of polyacetylenic
compounds; Nature, 168, 900-903.
(With T. Y. Shen, M. C. Whiting) Acetylenic compounds. XXXI. Some qualitative and quantitative
aspects of the Reppe carboxylation reaction; J. Chem. Soc., 766-771.
(With T. Y. Shen, M. C. Whiting) Acetylenic compounds. XXX. Catalytic and inhibitory effects in
the Reppe carboxylation reaction; J. Chem. Soc., 763-766.
(With T. Y. Shen, M. C. Whiting) Acetylenic compounds. XXIX. The reaction between nickel
carbonyl and disubstituted acetylenes; J. Chem. Soc., 48-52.
(With T. R. Ames, G. S. Davy, T. G. Halsall) Triterpenes. XII. Action of formic acid on lupeol; J.
Chem. Soc., 2868-2872.
(With J. B. Armitage, M. C. Whiting) Acetylenic compounds. XXXVII. The synthesis of conjugated
tetraacetylenic compounds; J. Chem. Soc., 2014-2018.
(With J. B. Armitage, C. L. Cook, M. C. Whiting) Acetylenic compounds. XXXVI. The synthesis of
symmetrical conjugated triacetylenic compounds; J. Chem. Soc., 2010-2014.
(With J. B. Armitage, C. L. Cook, N. Entwistle, M. C. Whiting) Acetylenic compounds. XXXIV.
Further studies on the synthesis of diacetylenic glycols; J. Chem. Soc., 1998-2005.
(With J. B. Armitage, M. C. Whiting) Acetylenic compounds. XXXIII. Preparation of mono
substituted derivatives of diacetylenes; J. Chem. Soc., 1993-1998.
(With P. Bladon, H. B. Henbest, G. W. Wood, G. F. Woods) Studies in the sterol group. LVII. Sidechain degradation of 3-acetoxy-5,8-epidioxy-9,22-ergostadiene; J. Chem. Soc., 4890-4894.
(With P. Bladon, R. B. Clayton, C. W. Greenhalgh, H. B. Henbest, B. J. Lovell, G. Silverstone, G. W.
Wood, G. F. Woods, et al.) Studies in the sterol group. LVI. Reduction of dehydroergosterol
epidioxide; J. Chem. Soc., 4883-4890.
(With J. B. Brown, H. B. Henbest) 3-Indolylacetaldehyde and 3-indolylacetone; J. Chem. Soc., 31723176.
(With J. B. Brown, H. B. Henbest) The synthesis and biological activity of 3-indolylacetaldehyde,
Nature, 169, 335.
(With C. L. Cook, M. C. Whiting) Acetylenic compounds. XXXIX. General routes to aliphatic
polyacetylenic hydrocarbons and glycols; J. Chem. Soc., 2883-2891.
(With G. Eglinton, M. C. Whiting) Acetylenic compounds. XXXVIII. New method for the
introduction of the acetylenic linkage; J. Chem. Soc., 2873-2882.
(With K. R. Farrar, J. C. Hamlet, H. B. Henbest) Polyene series. XLIII. The structure and synthesis of
vitamin A2 and related compounds; J. Chem. Soc., 2657-2668.
(With C. W. Greenhalgh, H. B. Henbest) Studies in the sterol group. LIV. Preparation of some 7methoxy steroids; J. Chem. Soc., 2380-2383.
Jones 6
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(156)
(157)
(158)
(159)
1953
(160)
(161)
(162)
(163)
(164)
(165)
(166)
(167)
(168)
(169)
(170)
(171)
(172)
(173)
(174)
(175)
(176)
(177)
(178)
(179)
(180)
(181)
(182)
(183)
(184)
(185)
(186)
1954
(With C. W. Greenhalgh, H. B. Henbest) Studies in the sterol group. LIII. The preparation of 7hydroxy-3-keto-4-steroids; J. Chem. Soc., 2375-2380.
(With T. G. Halsall, G. D. Meakins) Triterpenes. XI. Conversion of lupeol into germanicol
(isolupeol). Structure of lupeol hydrochloride; J. Chem. Soc., 2862-2868.
(With H. B. Henbest, G. W. Wood, G. F. Woods) Studies in the sterol group. LVIII. Oxidation of
5,8-epidioxy-9(11)-steroids; J. Chem. Soc., 4894-4896.
(With H. B. Henbest, G. F. Smith, J. A. Bentley) 3-Indoleacetonitrile: a naturally occurring plant
growth hormone; Nature, 169, 485-487.
(With J. L. Beton, A. Bowers, T. G. Halsall) Chemistry of the taraxasterol group of pentacyclic
triterpenes; Chem. and Ind., 847-848.
(With P. Bladon, H. B. Henbest, B. J. Lovell, G. F. Woods) Synthesis of cortical hormones via 5hydroxy steroids; Chem. and Ind., 945.
(With P. Bladon, H. B. Henbest, B. J. Lovell, G. W. Wood, G. F. Woods, J. Elks, R. M. Evans, D. E.
Hathway, et al.) Steroid group. LXII. Studies in the synthesis of cortisone. I. Novel route to 11-oxo
steroids; J. Chem. Soc., 2921-2933.
(With P. Bladon, H. B. Henbest, G. W. Wood, D. C. Eaton, A. A. Wagland) Steroid group. LXI.
Oxidation of 5-hydroxy- and 5-acetoxy-7,9-steroids; J. Chem. Soc., 2916-2921.
(With A. Bowers, T. G. Halsall, A. J. Lemin) Chemistry of the triterpenes and related compounds.
XVIII. Elucidation of the structure of polyporenic acid C; J. Chem. Soc., 2548-2560.
(With R. B. Clayton, H. B. Henbest) The steroid group. LX. Reduction of ergosterol epidioxide; J.
Chem. Soc., 2015-2021.
(With R. B. Clayton, A. Crawshaw, H. B. Henbest, B. J. Lovell, G. W. Wood) The steroid group.
LIX. Preparation and reactions of 5,8-epoxy-9(11)-steroids; J. Chem. Soc., 2009-2014.
(With R. G. Curtis, I. M. Heilbron, G. F. Woods) The chemistry of the triterpenes. XIII. Further
characterization of polyporenic acid A; J. Chem. Soc., 457-464.
(With M. C. Dawson, T. G. Halsall, P. A. Robins) The chemistry of the triterpenes. XVI. The action
of hydrogen chloride on butyrospermol; J. Chem. Soc., 586-589.
(With J. M. Guider, T. G. Halsall) Triterpenes and related compounds. XX. Stereochemistry of ring E
of betulin and related compounds; J. Chem. Soc., 3024-3028.
(With T. G. Halsall, R. Hodges) Triterpenes and related compounds. XIX. Further evidence
concerning the structure of polyporenic acid A; J. Chem. Soc., 3019-3024.
(With T. G. Halsall, A. J. Lemin) The chemistry of the triterpenes. XV. The environment of the
unreactive double bond of polyporenic acid A; J. Chem. Soc., 468-475.
(With H. B. Henbest, G. F. Smith) Isolation of a plant-growth hormone, 3-indoleacetonitrile; J. Chem.
Soc., 3796-3801.
(With G. Eglinton, M. C. Whiting) 4-Pentyn-1-ol; Org. Syntheses, 33, 68-69 [Collective Vol. 4, 1963,
755-757].
Recent work on polyacetylenes; Record Chem. Progr. (Kresge-Hooker Sci. Lab.), 1, 1-5.
(With J. D. Bu’Lock) Constituents of the higher fungi. III. Agrocybin; J. Chem. Soc., 3719-3720.
(With G. F. Woods) The chemistry of the triterpenes. XIV. Further evidence concerning the
unsaturated centers of polyporenic acid A; J. Chem. Soc., 464-468.
(With M. C. Whiting) The properties of penta-1,3-diyne; J. Chem. Soc., 3317.
(With T. R. Ames, J. L. Beton, A. Bowers, T. G. Halsall) The chemistry of the triterpenes and related
compounds. XXIII. The structure of taraxasterol, -taraxasterol (heterolupeol), and lupenol-I; J.
Chem. Soc., 1905-1919.
(With J. B. Armitage, N. Entwistle, M. C. Whiting) Acetylenic compounds. XLI. The synthesis of
diphenylpolyacetylenes; J. Chem. Soc., 147-154.
(With E. B. Bates, M. C. Whiting) Acetylenic compounds. XLII. Reductions with lithium aluminum
hydride; J. Chem. Soc., 1854-1860.
(With P. Bladon, H. B. Henbest, B. J. Lovell, G. F. Woods) Steroid group. LXIII. Synthesis of
cortisone acetate via 5-hydroxy steroids; J. Chem. Soc., 125-130.
(With J. D. Bu'Lock, G. H. Mansfield, J. W. Thompson, M. C. Whiting) Structures of two
polyacetylenic antibiotics; Chem. and Ind., 990-991.
(With A. Crawshaw, H. B. Henbest) Steroid group. LXV. Reactions of 11-hydroxy and 11-oxo 5steroids; J. Chem. Soc., 731-735.
(With G. Eglinton, G. H. Mansfield, M. C. Whiting) Acetylenic compounds. XLV. The alkaline
isomerization of but-3-ynoic acid; J. Chem. Soc., 3197-3200.
(With G. Eglinton, B. L. Shaw, M. C. Whiting) Acetylenic compounds. XLIII. A new method for the
preparation of alkoxyacetylenes; J. Chem. Soc., 1860-1865.
(With J. M. Guider, T. G. Halsall) Chemistry of the triterpenes and related compounds. XXVII.
Pinicolic acid A; J. Chem. Soc., 4471-4475.
(With J. M. Guider, T. G. Halsall, R. Hodges) Chemistry of the triterpenes and related compounds.
XXVI. The nature of polyporenic acid B; J. Chem. Soc., 3234-3238.
Jones 7
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(189)
(190)
(191)
(192)
(193)
(194)
1955
(195)
(196)
(197)
(198)
(199)
(200)
(201)
(202)
(203)
(204)
1956
(205)
(206)
(207)
(208)
(209)
(210)
(211)
(212)
(213)
(214)
(215)
(216)
(217)
1957
(With T. G. Halsall, R. E. H. Swayne) The chemistry of the triterpenes and related compounds. XXII.
The conversion of lupeol into -taraxasterol (heterolupeol); J. Chem. Soc., 1902-1905.
(With J. M. Thompson, M. C. Whiting) Synthesis of dodeca-1,11-diene-3,5,7,9-tetrayne; Acta Chem.
Scand., 8, 1944.
(With B. L. Shaw, M. C. Whiting) Acetylenic compounds. XLVIII. The prototropic rearrangements
of some diacetylenic dicarboxylic acids; J. Chem. Soc., 3212-3217.
(With G. H. Mansfield, M. C. Whiting) Acetylenic compounds. XLVII. The prototropic
rearrangements of some acetylenic dicarboxylic acids; J. Chem. Soc., 3208-3212.
(With G. H. Whitham, M. C. Whiting) Acetylenic compounds. XLVI. Prototropic rearrangements of
acetylenic acids; J. Chem. Soc., 3201-3208.
(With G. H. Whitham, M. C. Whiting) Acetylenic compounds. XLIV. The reaction between nickel
carbonyl and some esters of -acetylenic acids; J. Chem. Soc., 1865-1858.
(With G. Eglinton, M. C. Whiting, B. L. Shaw) Ethoxyacetylene; Org. Syntheses, 34, 46-49
[Collective Vol. 4, 1963, 404-407].
(With J. L. H. Allan, M. C. Whiting) Acetylenic compounds. XLIX. The preparation and ultraviolet
absorption spectra of the stereoisomeric conjugated hexadienoic and hexenynoic acids; J. Chem. Soc.,
1862-1873.
(With J. D. Bu'Lock, P. R. Leeming) Constituents of the higher fungi. V. The structures of nemotinic
acid and nemotin; J. Chem. Soc., 4270-4276.
(With J. D. Bu'Lock, W. B. Turner) Production of Compositae type polyacetylenes by a fungus;
Chem. and Ind., 686.
(With A. Crawshaw, H. B. Henbest, A. A. Wagland) Steroid group. LXX. Reactions at C-11 in 9steroids; J. Chem. Soc., 3420-3426.
(With M. C. Dawson, T. G. Halsall, G. D. Meakins, P. C. Phillips) Butyrospermol and “basseol;”
Chem. and Ind., 918-919.
(With H. B. Henbest, A. A. Wagland, T. I. Wrigley) Steroid group. LXIX. Bromination of 11-oxo5-steroids; J. Chem. Soc., 2477-2479.
(With H. B. Henbest, T. C. Owen) Polyene series. LI. Conversion of vitamin A1 into vitamin A2; J.
Chem. Soc., 2765-2767.
(With H. B. Henbest, T. C. Owen, V. Thaller) Polyene series. L. Anhydrovitamin A 2; J. Chem. Soc.,
2763-2765.
(With T. G. Halsall) Tetracyclic triterpenes; Fortsch. Chem. org. Naturstoffe, 12, 44-130.
(With P. C. Wailes, M. C. Whiting) Tetracarbonyliron bisphenylacetylide; J. Chem. Soc., 4021-4022.
(With I. Bell, M. C. Whiting) The synthesis of three naturally occurring polyacetylenic esters; Chem.
and Ind., 548-549.
(With J. L. Beton, T. G. Halsall) Chemistry of triterpenes and related compounds. XXVIII. Boswellic acid; J. Chem. Soc., 2904-2909.
(With J. D. Bu'Lock, P. R. Leeming, J. M. Thompson) Chemistry of the higher fungi. VI.
Isomerization reactions of naturally occurring allenes; J. Chem. Soc., 3767-7371.
(With R. Clarkson, P. C. Wailes, M. C. Whiting) The structure of the bridged iron complexes from
iron hydrocarbonyl and acetylenes; J. Am. Chem. Soc., 78, 6206-6207.
(With M. C. Dawson, T. G. Halsall, G. D. Meakins, P. C. Phillips) Chemistry of triterpenes and
related compounds. XXIX. Butyrospermol; J. Chem. Soc., 3172-3178.
(With D. Holme, M. C. Whiting) The synthesis of an all-cis-tetraene; Chem. and Ind., 928.
(With L. Skattebøl, M. C. Whiting) Investigations on acetylenic compounds. LIV. The preparation
and synthetical applications of ethynylmagnesium bromide; J. Chem. Soc., 4765-4768.
(With G. H. Mansfield, M. C. Whiting) Acetylenic compounds. LII. The preparation and anomalous
absorption spectra of some bicyclo[2.2.1]heptane derivatives; J. Chem. Soc., 4073-4082.
(With I. Bell, M. C. Whiting) Researches on acetylenic compounds. LVI. The stereochemical
consequences of some anionotropic rearrangements; J. Chem. Soc., 2597-2600.
(With J. L. Beton, T. G. Halsall, P. C. Phillips) Triterpenes and related compounds. XXX. The
relative stabilities of ring-A unsaturated hydrocarbons derived from 3,4-dimethylcholestane and 3methyl-24-nor-12-ursene; J. Chem. Soc., 753-765.
(With J. D. Bu'Lock, W. B. Turner) Chemistry of the higher fungi. VIII. A series of acetylenic
compounds from Polyporus anthracophilus; J. Chem. Soc., 1607-17.
(With J. D. Bu'Lock, P. R. Leeming) Chemistry of the higher fungi. VII. Odyssic acid and odyssin; J.
Chem. Soc., 1097-1101.
(With P. K. Christensen, N. A. Sørensen, I. Bell, M. C. Whiting) Constitution of the so-called
“composit-cumulene I” from scentless mayweed (Matricaria inodora); in Festschrift Arthur Stoll,
Sandoz, Basel, 545-550.
(With W. J. Dunstan, H. Fazakerley, T. G. Halsall) The chemistry of triterpenes and related
compounds. XXXII. The chemistry of hydroxyhopanone; Croat. Chem. Acta, 29, 173-182.
Jones 8
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(220)
(221)
(222)
(223)
1958
(224)
(225)
(226)
(227)
(228)
(229)
1959
(230)
(231)
(232)
(233)
(234)
(235)
(236)
(237)
1960
(238)
(239)
(240)
(241)
(242)
(243)
(244)
(245)
(246)
(247)
(248)
(249)
(250)
(251)
1961
(With H. B. Henbest, T. C. Owen) Studies in the polyene series. LII. Oxidation of vitamin A 1, and
retinene1, by manganese dioxide; J. Chem. Soc., 4909-4912.
(With G. H. Whitham, M. C. Whiting) Acetylenic compounds. LVII. A general synthesis of allenic
acids; J. Chem. Soc., 4628-4633.
(With W. C. Taylor) Some indole constituents of cabbage; Nature, 179, 1138.
(With J. M. Thompson, M. C. Whiting) Acetylenic compounds. LV. The preparation and properties
of some polyacetylenic acids, and their derivatives; J. Chem. Soc., 2012-2017.
(With K. Schaffner, L. Caglioti, D. Arigoni, O. Jeger, H. Fazakerley, T. G. Halsall) The structure of
hydroxyhopanone; Proc. Chem. Soc., 353-354.
(With P. J. Ashworth, G. H. Mansfield, K. Schlogl, J. M. Thompson, M. C. Whiting) Researches on
acetylenic compounds. LIX. The synthesis of three polyacetylenic antibiotics; J. Chem. Soc., 950954.
(With I. Bell, M. C. Whiting) Acetylenic compounds. LXI. The synthesis of three polyacetylenic
esters; J. Chem. Soc., 1313-1322.
(With J. Castells, R. W. J. Williams, G. D. Meakins) The stereochemistry of lumisterol and
pyrocalciferol; Proc. Chem. Soc., 7-8.
(With J. S. G. Cox, L. B. High) Determination of steroid side-chains, Proc. Chem. Soc., 234-235.
(With G. D. Meakins, J. S. Stephenson) Steroid group. LXXI. Preparation and reactions of 9methylergostane derivatives; J. Chem. Soc., 2156-2166.
(With L. Skattebøl, M. C. Whiting) Researches on acetylenic compounds. LX. The synthesis of three
natural polyacetylenic hydrocarbons; J. Chem. Soc., 1054-1059.
(With J. R. Case, R. Clarkson, M. C. Whiting) New iron-acetylene-carbonyl complexes; Proc. Chem.
Soc., 150.
(With J. Castells, G. D. Meakins, R. W. J. William) Steroids of natural configuration. I.
Stereochemistry of lumisterol and 9-lumisterol (pyrocalciferol); J. Chem. Soc., 1159-1168.
(With H. Fazakerley, T. G. Halsall) Chemistry of triterpenes and related compounds. XXXIV.
Structure of hydroxyhopanone; J. Chem. Soc., 1877-1883.
(With J. Fishman, G. Lowe, M. C. Whiting) Structure and biogenesis of trichothecin; Proc. Chem.
Soc., 127-128.
(With J. S. Stephenson) Chemistry of the higher fungi. IX. Polyacetylenic metabolites from Coprinus
quadrifidus; J. Chem. Soc., 2197-2203.
(With D. J. Wluka) Steroid series. LXXIII. Bromination of 7-oxosteroids; J. Chem. Soc., 911-915.
(With D. J. Wluka) Steroid series. LXXII. Bromination of 11-oxo-5-steroids; J. Chem. Soc., 907-11.
(With L. Skattebøl, M. C. Whiting) 1-Phenyl-1-penten-4-yn-3-ol; Org. Syntheses, 39, 56-59
[Collective Vol. 4, 1963, 792-795].
(With G.. V. Baddeley, T. G. Halsall) Chemistry of triterpenes and related compounds. XXXVII.
Stereochemistry of the D/E ring junction of hydroxyhopanone; J. Chem. Soc., 1715-1718.
(With J. Castells, G. A. Fletcher, G. D. Meakins, R. Swindells) Steroids of unnatural configuration.
III. Dihydro and tetrahydro derivatives of lumisterol; J. Chem. Soc., 2785-2792.
(With J. Castells, G. A. Fletcher, G. D. Meakins, R. Swindells) Steroids of unnatural configuration. II.
Reduction products of lumisterol: Hexahydro compounds; J. Chem. Soc., 2627-2639.
(With J. Fishman, G. Lowe, M. C. Whiting) The chemistry and stereochemistry of trichothecin; J.
Chem. Soc., 3948-3959.
(With J. N. Gardner, P. R. Leeming, J. S. Stephenson) Chemistry of the higher fungi. X. Further
polyacetylenic derivatives of decane from various basidiomycetes; J. Chem. Soc., 691-697.
(With J. B. Jones, L. Skattebøl, M. C. Whiting) Acetylenic compounds. LXV. Synthesis of odyssin A
and iso-odyssic lactone; J. Chem. Soc., 3489-3493.
(With H. H. Lee, M. C. Whiting) Acetylenic compounds. LXIV. The preparation of conjugated octaand decaacetylenic compounds; J. Chem. Soc., 3483-3489.
(With H. H. Lee, M. C. Whiting) Acetylenic compounds. LXII. The preparation and some synthetic
applications of penta-1,2,4-triene and penta-1,2-dien-4-yne; J. Chem. Soc., 341-346.
(With J. D. Loder, M. C. Whiting) The absolute configuration of an optically active allene, Proc.
Chem. Soc., 180-181.
(With G. Lowe) Biogenesis of trichothecin; J. Chem. Soc., 3959-3962.
(With P. R. Leeming, W. A. Remers) Chemistry of the higher fungi. XI. Polyacetylenic metabolites of
Drosophila subatrata; J. Chem. Soc., 2257-2263.
Polyacetylenes; Proc. Chem. Soc., 199-210.
(With M. C. Whiting) Einige Bemerkungen zu der Mitteilung “Von aliphatischen
Acetylenkohlenwasserstoffen ausgehende Synthesen” von Theo Herbertz; Chem. Ber., 93, 761-762.
(With G. V. Baddeley, T. G. Halsall) Chemistry of triterpenes and related compounds. XL. Final
clarification of the stereochemistry of hydroxyhopanone; J. Chem. Soc., 3891-3893.
(With B. M. Baird, T. G. Halsall, G. Lowe) Cephalosporin P1; Proc. Chem. Soc., 257-258.
Jones 9
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(253)
(254)
1962
(255)
(256)
(257)
1963
(258)
(259)
(260)
(261)
(262)
1964
(263)
(264)
(265)
(266)
1965
(267)
(268)
(269)
(270)
(271)
(272)
(273)
(274)
(275)
(276)
(277)
(278)
(279)
(280)
(281)
1966
(With G. R. Chaudhry, T. G. Halsall) Chemistry of the triterpenes and related compounds. XXXIX.
Some derivatives of 4,4-dimethylcholestan-3-one; J. Chem. Soc., 2725-2732.
(With S. R. Gupta, T. G. Halsall) Chemistry of triterpenes and related compounds. XLI. Bromination
of lupeol and its esters; J. Chem. Soc., 5353-5359.
(With R. Case, N. V. Schwartz, M. C. Whiting) Geometry of binuclear Fe carbonyl complexes,
(RCCR')H2Fe2(CO)8; Proc. Chem. Soc., 256-257.
(With J. Castells, G. D. Meakins, S. Palmer, R. Swindells) Steroids of unnatural configuration. VII.
Reduction products of 9-lumisterol (pyrocalciferol); J. Chem. Soc., 2907-2916.
(With M. P. Hartshorn) Studies in the steroid series. LXXIV. Some tricyclic analogs of steroid sex
hormones; the bromination of enol acetates; J. Chem. Soc., 1312-1313.
(With R. C. Cambie, A. Hirschberg, G. Lowe) Chemistry of the higher fungi. XVI. Polyacetylenic
metabolites from Aleurodiscus roseus; J. Chem. Soc., 4120-41230.
(With R. C. Cambie, G. Lowe) Chemistry of the higher fungi. XV. Synthesis of two -hydroxy acids
from Poria sinuosa; J. Chem. Soc., 3466-3468.
(With R. C. Cambie, J. N. Gardner, G. Lowe, G. Read) Chemistry of the higher fungi. XIV.
Polyacetylenic metabolites of Poria sinuosa; J. Chem. Soc., 2056-2064.
(With T. G. Halsall, G. Lowe) The molecular formula of cephalosporin P 1; Proc. Chem. Soc., 16.
(With J. S. Stephenson, W. B. Turner, M. C. Whiting) Chemistry of the higher fungi. XIII. Synthesis
of (a) a C9 triacetylenic epoxy alcohol, a Coprinus quadrifidus metabolite, and (b) a C 9 triacetylenic
1,2-diol. The structure of biformyne I; J. Chem. Soc., 2048-2055.
(With G. V. Baddeley, T. G. Halsall) Chemistry of triterpenes and related compounds. XLIV.
Conversion of lupeol into an enantiomer of 4,9-dimethyl-5-androstan-3-one; J. Chem. Soc.,
1173-1181.
(With S. Binns, J. S. G. Cox, B. G. Ketcheson) Steroid group. LXXV. Partial synthesis of 4,9dimethyl-5-androstan-3-one, the enantiomer of a triterpene degradation product; J. Chem. Soc.,
1161-1173.
(With W. A. Harrison, G. D. Meakins, P. A. Wilkinson) Nitro steroids. I. The reaction of cholesteryl
acetate with nitrosyl chloride; J. Chem. Soc., 3210-3214.
(With B. E. Lowe, G. Lowe) Chemistry of the higher fungi. XVII. Polyacetylenic metabolites from
Clitocybe rhizophora; J. Chem. Soc., 1476-1481.
(With J. R. Bull, G. D. Meakins) Nitro steroids. II. A new route to nitro steroids; J. Chem. Soc., 26012614.
(With C. Chin, V. Thaller, R. T. Aplin, L. J. Durham, S. C. Cascon, W. B. Mors, B. M. Tursch) Toxic
C14 polyacetylenic tetrahydropyranyl alcohol from the Compositae; Chem. Commun., 152-154.
(With C. H. Fawcett, D. M. Spencer, R. L. Wain, M. Le Quan, C. B. Page, V. Thaller) Antifungal
acetylenic oxoester from a plant of the Papilionaceae family;Chem. Commun., 422-423.
(With D. A. Wilson) Studies in the steroid group. LXXVI. The methylation of enol acetates and
bromo ketones. Nuclear magnetic resonance spectra of 11-oxo steroids; J. Chem. Soc., 2933-2944.
(With R. E. Bew, R. C. Cambie, G. Lowe) Natural acetylenes. XIX. Metabolites from some Poria
species; J. Chem. Soc. C, 135-138.
(With R. E. Bew, J. R. Chapman, B. E. Lowe, G. Lowe) Natural acetylenes. XVIII. Some allenic
polyacetylenes from basidiomycetes; J. Chem. Soc. C, 129-135.
(With J. E. Bridgeman, P. C. Cherry, W. R. T. Cottrell, P. W. Le Quesne, G. D. Meakins) Relative
stabilities of cis- and trans-A/B-1,6-dioxosteroids; Chem. Commun., 561-562.
(With P. C. Cherry, G. D. Meakins) Microbiological hydroxylation at position 3 of androst-5-en-7one; Chem. Commun., 587-588.
(With T. G. Halsall, G. Lowe, C. E. Newall) Cephalosporin P 1; Chem. Commun., 685-687.
(With T. G. Halsall, E. L. Tan, G. R. Chaudhry) The chemistry of triterpenes and related compounds.
XLV. The acid-catalyzed rearrangements of the 5,6-diols and 5,6-epoxides of some 4,4dimethylsteroids; J. Chem. Soc. C, 1374-1383.
(With P. Hodge, G. Lowe) Natural acetylenes. XXII. trans-Dehydromatricaria ester as a biosynthetic
precursor of some fungal polyacetylenes; J. Chem. Soc., C, 1216-1219.
(With R. Mestres) Cyclization of -substituted -phenylcinnamaldehydes; An. R. Soc. Esp. Fis.
Quim., Ser. B, 62(B), 377-384.
(With S. Safe, V. Thaller) Natural acetylenes. XXIII. A C18 polyacetylenic oxo aldehyde related to
falcarinone from an umbellifer (Pastinaca sativa); J. Chem. Soc. C, 1220-1221.
(With G. Lowe, P. V. R. Shannon) Natural acetylenes. XXI. The biosynthesis and transformation of
some polyacetylenic metabolites of Merulius lacrymans and Clitocybe rhizophora; J. Chem. Soc., C,
144-148.
Natural polyacetylenes and their precursors; Chemistry in Britain, 6-13.
(With G. Lowe, P. V. R. Shannon) Natural acetylenes. XX. Tetraacetylenic and other metabolites
from Fistulina hepatica; J. Chem. Soc. C., 139-144.
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1970
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1971
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1972
(With R. W. Bradshaw, A. C. Day, C. B. Page, V. Thaller) Synthesis of crepenyic acid; Chem.
Commun., 1055-106.
(With J. E. Bridgeman, G. D. Meakins, J. Wicha) Convenient preparation of 5-androstan-16-one;
Chem. Commun., 898.
(With J. E. Bridgeman, P. C. Cherry, G. D. Meakins) Microbiological hydroxylation as a route to 5androstan-1-one; Chem. Commun., 482-483.
(With J. R. F. Fairbrother, V. Thaller) Natural acetylenes. XXV. The biosynthesis of benzenoid
polyacetylenes; J. Chem. Soc. C, 1035-1038.
(With S. Safe, V. Thaller) Natural acetylenes. XXVI. Transformations of phenyl polyacetylenes in the
tubers of Dahlia hybrids; J. Chem. Soc. C, 1038-1041.
(With C. H. Fawcett, D. M. Spencer, R. L. Wain, A. G. Fallis, M. Le Quan, C. B. Page, V. Thaller, D.
C. Shubrook, P. M. Whitham) Natural acetylenes. XXVII. An antifungal acetylenic furanoid ketoester (Wyerone) from shoots of the broad bean (Vicia faba fam. Papilionaceae); J. Chem. Soc. C,
2455-2462.
(With G. D. Meakins, K. Z. Tuba, P. D. Woodgate) Simple route to 17-aza-5-androstan-16-one;
Chem. Commun., 210-211.
(With R. K. Bentley, V. Thaller) Natural acetylenes. XXX. Polyacetylenes from Lactuca (lettuce)
species of the Liguliflorae subfamily of the Compositae; J. Chem. Soc. C, 1096-1099.
(With R. K. Bentley, J. K. Jenkins, V. Thaller) Natural acetylenes. XXIX. Polyacetylenes from the
Campanulaceae plant family. Tetrahydropyranyl polyacetylenic alcohols from the clustered
bellflower (Campanula glomerata); J. Chem. Soc. C, 830-832.
(With R. K. Bentley, U. Graf, R. A. M. Ross, V. Thaller, R. A. V. Hodge) Dimerization of
polyacetylenic aldehydes with elimination of carbon monoxide; J. Chem. Soc. C, 683-635.
(With R. K. Bentley, D. Bhattacharjee, V. Thaller) Natural acetylenes. XXVIII. C17-polyacetylenic
alcohols from the umbellifer Daucus carota (carrot): alkylation of benzene by
acetylenyl(vinyl)carbinols in the presence of p-toluenesulfonic acid; J. Chem. Soc. C, 685-688.
(With J. E. Bridgeman, J. W. Browne, P. C. Cherry, M. G. Combe, J. M. Evans, A. Kasal, G. D.
Meakins, Y. Morisawa, P. D. Woodgate) Hydroxylation of nine simple steroid ketones (monooxo-5androstanes) with cultures of the fungus, Calonectria decora; Chem. Commun., 463-464.
(With J. M. Evans, A. Kasal, V. Kumar, G. D. Meakins, J. Wicha) 16-Hydroxylation of steroids with
the fungus Rhizopus nigricans; Chem. Commun., 1491.
(With A. G. Fallis, V. Thaller) A route to the polyacetylenic C 18-acids containing 1-en-4-yne
unsaturation; Chem. Commun., 924-925.
(With G. D. Meakins, K. Z. Tuba) Studies in the steroid group. LXXIX. Preparation of 2-aza-3-oxo,
3-aza-2-oxo-, 16-aza-17-oxo-, and 17-aza-16-oxo-5-androstane, and of 3-aza-2-oxo-5-cholestane;
J. Chem. Soc. C, 1597-1602.
(With J. E. Bridgeman, C. E. Butchers, A. Kasal, G. D. Meakins, P. D. Woodgate) Steroid group.
LXXX. Preparation of 2- and 16-oxo-, and 3,16- and 2,16-dioxo-5-androstane, and 2-oxo-5cholestane; J. Chem. Soc. C, 244-250.
(With J. E. Bridgeman, P. C. Cherry, A. S. Clegg, J. M. Evans, A. Kasal, V. Kumar, G. D. Meakins,
Y. Morisawa, E. E. Richards, P. D. Woodgate) Microbiological hydroxylation of steroids. I. Proton
magnetic resonance spectra of ketones, alcohols, and acetates in the androstane, pregnane, and
oestrane series; J. Chem. Soc. C, 250-257.
(With C. Chin, M. C. Cutler, J. Lee, S. Safe, V. Thaller) Natural acetylenes. XXXI. C 14tetrahydropyranyl and other polyacetylenes from the compositae Dahlia coccinea Cav. var coccinea;
J. Chem. Soc. C, 314-322.
(With A. S. Clegg, G. D. Meakins, J. T. Pinhey) Preparation of 1,11-dihydroxysteroids by
microbiological hydroxylation; Chem. Commun., 1029.
(With J. W. Blunt, I. M. Clark, J. M. Evans, G. D. Meakins, J. T. Pinhey) Microbiological
hydroxylation of steroids. III. A convenient microbiological route to 15-oxygenated 5--androstanes;
J. Chem. Soc. C, 1136-1138.
(With G. C. Barley, A. C. Day, U. Graf, I. O'Neill, R. Tachikawa, V. Thaller, R. A. Vere Hodge)
Natural acetylenes. XXXIII. Biogenesis of the C9 diacetylenic triol from the fungus Clitocybe
rhizophora; J. Chem. Soc. C, 3308-3313.
(With R. W. Bradshaw, A. C. Day, C. B. Page, V. Thaller, R. A. V. Hodge) Natural acetylenes.
XXXII. Synthesis of crepenynic acid (9-octadecen-12-ynoic acid); J. Chem. Soc. C,1156-1158.
(With A. M. Bell, J. W. Browne, W. A. Denny, A. Kasal, G. D. Meakins) Microbiological
hydroxylation of steroids. VI. Hydroxylation of simple mono- and dioxygenated 5-androstanes and
of 3-oxoestranes with the fungus Aspergillus ochraceus; J. Chem. Soc., Perkin I, 2930-2936.
(With A. M. Bell, W. A. Denny, G. D. Meakins, W. E. Mueller) Microbiological hydroxylation of
steroids. V. Pattern of hydroxylation of dioxygenated 5-androstanes with cultures of the fungus
Calonectria decora; J. Chem. Soc., Perkin I, 2759-2765.
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1974
(With A. M. Bell, P. C. Cherry, I. M. Clark, W. A. Denny, G. D. Meakins, P. D. Woodgate)
Microbiological hydroxylation of steroids. IV. Pattern of dihydroxylation of monooxygenated 5androstanes with cultures of the fungus Calonectria decora; J. Chem. Soc., Perkin I, 2081-2095.
(With I. M. Clark, W. A. Denny, G. D. Meakins, A. Pendlebury, J. T. Pinhey) Steroid group.
LXXXIV. Preparation and reactions of 15-oxygenated androstanes; J. Chem. Soc., Perkin I, 27652770.
(With I. M. Clark, A. S. Clegg, W. A. Denny, G. D. Meakins, A. Pendlebury) Steroid group.
LXXXIII. 1-, 2-, 3-, 4-, 6-, 12-, -5-, and 16-Monohydroxy-5-androstanes and their derivatives; J.
Chem. Soc., Perkin I, 499-502.
(With A. S. Clegg, W. A. Denny, V. Kumar, G. D. Meakins, V. E. M. Thomas) Steroid group.
LXXXII. Preparation of nine mono- and eight dioxoandrostanes, 5-estran-17-one, and 5-pregnane2,20-dione; J. Chem. Soc., Perkin I, 492-498.
(With S. O. Badanyan, R. K. Bentley, J. K. Jenkins, V. Thaller) Natural acetylenes. XXXVII.
Polyacetylenes from the Campanulaceae plant family. Tetrahydropyranyl and open chain C 14
polyacetylenic alcohols from Campanula pyramidalis L. and Campanula medium L.; J. Chem. Soc.,
Perkin I, 145-147.
(With G. C. Barley, V. Thaller, R. A. V. Hodge) Natural acetylenes. XXXIX. Synthesis of methyl
[1,9-14C]-, [9,14C]-, and [10-3H]-crepenynate, methyl [9-14C]- and [10-3H]-linoleate, and methyl [914
C]- and [10-3H]-oleate; J. Chem. Soc., Perkin I, 151-154.
(With A. M. Bell, I. M. Clark, W. A. Denny, G. D. Meakins, W. E. Mueller, E. E. Richards)
Microbiological hydroxylation of steroids. IX. Hydroxylation of diketones and keto alcohols derived
from 5-androstane with the fungi Rhizopus arrhizus and Rhizopus circinnans. Steroidal 18- and 19proton magnetic resonance signals; J. Chem. Soc., Perkin I, 2131-2136.
(With R. K. Bentley, R. A. M. Ross, V. Thaller) Natural acetylenes. XXXVI. Polyacetylenes from the
Lobeliaceae plant family. C14 enediyne triol from Lobelia cardinalis; J. Chem. Soc., Perkin I, 140144.
(With J. W. Browne, W. A. Denny, G. D. Meakins, Y. Morisawa, A. Pendlebury, J. Pragnell)
Microbiological hydroxylation of steroids. VII. The pattern of dihydroxylation of mono-oxo-5androstanes and 5-estranes with the fungus Rhizopus nigricans; J. Chem. Soc., Perkin I, 1493-1499.
(With V. E. Chambers, W. A. Denny, J. M. Evans, A. Kasal, G. D. Meakins, J. Pragnell)
Microbiological hydroxylation of steroids. VIII. The pattern of monohydroxylation of diketones and
keto-alcohols derived from 5-androstane with cultures of the fungus, Rhizopus nigricans; J. Chem.
Soc., Perkin I, 1500-1511.
(With A. S. Clegg, W. A. Denny, G. D. Meakins, J. T. Pinhey) Microbiological hydroxylation of
steroids. X. 1 , 11 -dihydroxylation of 3-hydroxy-5-pregnan-20-one and the hydroxylation of
other 20-oxo-5-pregnanes with the fungus Aspergillus ochraceus; J. Chem. Soc., Perkin I, 21372141.
(With A. G. Fallis, M. T. W. Hearn, V. Thaller, J. L. Turner) Natural acetylenes. XL. Syntheses of
polyacetylenic C18 and C16 esters with 9-ene-12,14-diyne unsaturation, and their labelling; J. Chem.
Soc., Perkin I, 743-749.
(With M. T. W. Hearn, M. G. Pellatt, V. Thaller, J. L. Turner) Natural acetylenes. XLII. Novel C7, C8,
C9, and C10 polyacetylenes from fungal cultures; J. Chem. Soc., Perkin I, 2785-2788.
Microbiological hydroxylation of steroids and related compounds; Pure Appl. Chem., 33, 39-52.
(With J. W. Keeping, M. G. Pellatt, V. Thaller) Natural acetylenes. XXXVIII. Biosyntheses of
acetylenedicarboxamide (cellocidin) in Streptomyces SF-536 cultures; J. Chem. Soc., Perkin I, 148150.
(With M. Ahmed, G. C. Barley, M. T. W. Hearn, V. Thaller, J. A. Yates) Natural acetylenes. XLIII.
Polyacetylenes from cultures of the fungus Fistulina pallida; J. Chem. Soc., Perkin I, 1981-1987.
(With M. J. Ashton, A. S. Bailey) Microbiological hydroxylation. XII. Comparative behavior of Dhomogonane (perhydrochrysene) ketones and steroids; J. Chem. Soc., Perkin I, 1658-65.
(With M. J. Ashton, A. S. Bailey) Microbiological hydroxylation. XIII. Cyclododecanone and
cyclopentadecanone as substrates for steroid-hydroxylating fungi; J. Chem. Soc., Perkin I, 1665-1669.
(With A. M. Bell, V. E. Chambers, G. D. Meakins, W. E. Muller, J. Pragnell) Microbiological
hydroxylation of steroids. XI. Convenient routes to 3,7-, 3,11-, 3,12-, 7,11-, 7,17-, and 11,17dioxygenated 5-androstanes and to 5-androstan-11-one; J. Chem. Soc., Perkin I, 312-317.
(With R. K. Bentley, C. A. Higham, J. K. Jenkins, V. Thaller) Natural acetylenes. XLIV. C14
polyacetylenes from Trachelium caeruleum L. (Campanulaceae); J. Chem. Soc., Perkin I, 1987-1991.
(With F. Blaney, D. E. Johnston, M. A. McKervey, J. Pragnell) Hydroxylation of diamantan-1- and 4-ol with the fungus Rhizopus nigricans; J. Chem. Soc., Chem. Commun., 297-298.
(With M. T. W. Hearn, V. Thaller, J. L. Turner) Natural acetylenes. XLVI. Polyacetylenes from
cultures of the fungus Lepista glaucocana (Bres.) Singer; J. Chem. Soc., Perkin I, 2335-2336.
(With C. A. Higham, J. W. Keeping, V. Thaller) Natural acetylenes. XLV. Polyacetylenes from
cultures of the fungus Collybia peronata Bolt. ex Fr. Kummer; J. Chem. Soc., Perkin I, 1991-1994.
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1977
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1978
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1979
(With V. Thaller) Developments in natural polyacetylenes; An. Quim., 70, 1009-1014.
(With G. D. Meakins, J. Pragnell, W. E. Mueller, A. L. Wilkins) Studies in the steroid group.
LXXXV. Convenient preparations of 3,6- and 6,17-dioxygenated 5-androstanes; J. Chem. Soc.,
Perkin I, 2376-2380.
(With A. M. Bell, G. D. Meakins, J. O. Miners, A. L. Wilkins) Microbiological hydroxylation. XX.
Hydroxylation of dioxygenated 5-androstanes with the fungi Absidia regnieri and Syncephelastrum
racemosum; J. Chem. Soc., Perkin I, 2040-2043.
(With A. M. Bell, A. D. Boul, G. D. Meakins, J. O. Miners, A. L. Wilkins) Microbiological
hydroxylation. XVIII. Introduction of 16, 9-, and 3-hydroxy-groups into dioxygenated 5androstanes by the fungus Diaporthecelastrina; J. Chem. Soc., Perkin I, 1364-1366.
(With A. M. Bell, G. D. Meakins, J. O. Miners, A. Pendlebury) Microbiological hydroxylation. XV.
Hydroxylation in the terminal rings of mono- and dioxygenated 5-androstanes with the fungus
Daedalea rufescens; J. Chem. Soc., Perkin I, 357-360.
(With V. E. M. Chambers, G. D. Meakins, J. O. Miners, J. T. Pinhey, A. L. Wilkins) Microbiological
hydroxylation. XVII. Carbon-19 hydroxylation of 17-oxo-5-androstanes and 17-oxo-3,5-cyclo-5androstanes by the fungus Calonectria decora; J. Chem. Soc., Perkin I, 1359-1363.
(With V. E. M. Chambers, G. D. Meakins, J. O. Miners, A. L. Wilkins) Microbiological
hydroxylation. XIV. Hydroxylation in the terminal rings of dioxygenated 5-androstanes with the
fungi Wojnowicia graminis and Ophiobolus herpotrichus; J. Chem. Soc., Perkin I, 55-58.
(With J. M. Evans, G. D. Meakins, J. O. Miners, A. Pendlebury, A. L. Wilkins) Microbiological
hydroxylation. Part XVI. Incubation of derivatives (mainly acetals) of 5-androstane ketones with the
fungi Calonectria decora, Aspergillus ochraceus, and Rhizopus nigricans; J. Chem. Soc., Perkin I,
1356-1359.
(With G. D. Meakins, J. O. Miners, A. L. Wilkins) Microbiological hydroxylation. XXI.
Hydroxylations of 3-halo-17-oxo-3-halo-7-oxo-, and 17-halo-3-oxoandrostanes by the fungi
Calonectria decora, Rhizopus nigricans, and Aspergillus ochraceus; J. Chem. Soc., Perkin I, 23082312.
(With G. D. Meakins, J. O. Miners, J. H. Pragnell, A. L. Wilkins) Microbiological hydroxylation.
XIX. Action of an ant fungus (Acromyrmex fungus) on oxygenated androstanes, pregnanes, and
cholestanes; J. Chem. Soc., Perkin I, 1552-1554.
(With V. Thaller, J. L. Turner) Natural acetylenes. XLVII. Biosynthetic experiments with the fungus
Lepista diemii Singer. Biogenesis of the C8 acetylenic cyano acid diatretyne 2; J. Chem. Soc., Perkin
I, 424-428.
(With C. T. Bedford, D. Bhattacharjee, J. R. F. Fairbrother, S. Safe, V. Thaller) Natural acetylenes.
XLIX. Polyacetylenes from Dahlia scapigera (A. Dietr.) Link and Otto var. scapigera f. scapigera and
some Dahlia hybrids; J. Chem. Soc., Perkin I, 735-741.
(With W. A. Denny, P. M. Fredericks, I. Ghilezan, G. D. Meakins, J. O. Miners) 16,18Dihydroxylation of oxygenated 5-androstanes with the fungus Leptoporus fissilis; Chem. Commun.,
900-901.
(With I. Ghilezan, G. D. Meakins, J. O. Miners) Preparation of 3-hydroxy-5-androstan-16-one; J.
Chem. Soc., Perkin I, 1350-1351.
(With G. D. Meakins, J. O. Miners, R. N. Mirrington, A. L. Wilkins) Microbiological hydroxylation.
XXII. Hydroxylation of 3,20-, 7,20-, and 11,20-dioxygenated 5-pregnanes; J. Chem. Soc., Perkin I,
1842-1847.
(With M. Ahmed, M. T. W. Hearn, V. Thaller) Natural acetylenes. LI. Biosynthetic studies with C18
acetylenic precursors in fungal cultures. Origin of the carbon skeletons of mycomycin and
drosophilins C and D; J. Chem. Res. S, 125.
(With A. S. Bailey, M. L. Gilpin) Microbiological hydroxylation. Part 23. Bicyclic substrates for
steroid-hydroxylating fungi; J. Chem. Soc., Perkin I, 265-270.
(With A. S. Bailey, M. L. Gilpin) Microbiological hydroxylation. Part 22. Preparation of some
bicyclic substrates containing 15-16 carbon atoms; J. Chem. Soc., Perkin I, 259-265.
(With C. M. Piggin, V. Thaller, J. L. Turner) Natural acetylenes. L. The origin of the carbon skeletons
of C8 fungal polyacetylenes and the C8 thiophene acetylene, junipal; J. Chem. Res. S, 68-69.
(With V. Thaller) Natural acetylenes; Chapter 14 in The Chemistry of the Carbon-Carbon Triple
Bond (ed. S. Patai), Wiley, Chichester, 621-633.
(With V. Thaller) Polyacetylene compounds; Chapter 5.5 in part 3 (Steroids etc) of Methodicum
Chimicum, 11, 175-179.
(With T. G. C. Bird, G. Felsky, P. M. Fredericks, G. D. Meakins) Studies in the steroid group. Part
86. Preparation of oxygenated monofluoro- and gem-difluoro-5-androstanes using
diethylaminosulfur trifluoride and tetra-n-butylammonium fluoride; J. Chem. Res. S., 388-389.
(With T. G. C. Bird, P. M. Fredericks, G. D. Meakins) Convenient general preparation of oxygenated
monofluoro- and gem-difluoro-5-androstanes using diethylaminosulfur trifluoride; Chem. Commun.,
65-66.
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(362) 1945
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1947
1948
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1950
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1951
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1952
(With T. G. C. Bird, P. M. Fredericks, G. D. Meakins) Microbiological hydroxylation. Part 23.
Hydroxylations of fluoro-5-androstanones by the fungi Calonectria decora, Rhizopus nigricans, and
Aspergillus ochraceus; J. Chem. Soc., Perkin I, 750-755.
(With W. A. Denny, P. M. Fredericks, I. Ghilezan, G. D. Meakins, J. O. Miners) Microbiological
hydroxylation. Part XXIV. 16,18-Dihydroxylation of oxygenated 5-androstanes by the fungus
Leptoporus fissilis, J. Chem. Res. S., 20-21.
(With M. Ahmed, M. Y. Jarrah, A. F. Magalhaes, M. G. Roberts, V. Thaller) Natural acetylenes. Part
57. The isolation of polyacetylenic amino acids from cultures of the Tricholomataceae fungus
Fayodia bisphaerigera (J. Lange) Singer: synthesis of N-alkynoyl alanine and glycine methyl esters; J.
Chem. Res. S., 262-263.
(With T. A. Macrides, V. Thaller) Natural acetylenes. Part 56. Biosynthetic experiments with the
fungus Lepista diemii (Singer). Origin of the nitrile group of the C 8 acetylenic cyano-acid, diatretyne
2; J. Chem. Res. S., 157.
(With M. Ahmed, G. J. Broad, A. A. Taha, V. Thaller) Natural acetylenes. Part 58. Polyacetylenic
isoprenyl ethers from cultures of the fungus Fayodia bisphaerigera (J. Lange) Singer. Isolation and
synthesis; J. Chem. Res. S., 199.
(With G. C. Barley, U. Graf, C. A. Higham, M. Y. Jarrah, I. O'Neill, R. Tachikawa, V. Thaller, J. L.
Turner) Natural acetylenes. Part 61. Fungal polyacetylenes and the crepenynate pathway: the
biosynthesis of some C9-C14 polyacetylenes in fungal cultures; J. Chem. Res. S., 232-233.
(With S. G. Errington, I. W. Farrell, T. G. Halsall, M. T. W. Hearn, V. Thaller) A nor-sesquiterpenoid
acid from cultures of the fungus Lepista glaucocana (Bres.) singer; J. Chem. Res. S., 47.
(With I. W. Farrell, C. A. Higham, V. Thaller) Natural acetylenes. Part 62. Fungal polyacetylenes and
the crepenynate pathway: experiments relevant to the biogenesis of the acetylenic bond; J. Chem.
Res., 234-235.
(With G. C. Barley, V. Thaller) Crepenynate as a precursor of falcarinol in carrot tissue culture; in
Bioactive Molecules. Vol 7. Chemistry and Biology of Naturally-Occurring Acetylenes and Related
Compounds, Elsevier, Amsterdam, 85-91.
(With J.T. McCombie) Unsaturated alcohols (Imperial Chemical Industries Ltd.). GB560081.
(With J.T. McCombie) New unsaturated alcohols and their esters and ethers (Imperial Chemical
Industries Ltd.). GB571777.
(With R.W. Peevers) 7-Dehydrosterols (Glaxo Laboratories Ltd.). GB574432.
(With J.T. McCombie) 1-Alkoxy-2,4-pentadienes (Imperial Chemical Industries Ltd.). US2429411.
(With I.M. Heilbron) 2,5-Dimethylfuran and acetonylacetone. GB611072.
(With A.E. Bide, R.J. Nicholls) 7-Chlorocholesteryl acetate and 7-dehydrocholesterol (Glaxo
Laboratories Ltd.). GB608482.
(With I.M. Heilbron) Alkynylalkenylcarbinols. GB633972.
(With I.M. Heilbron) Cyclohexene derivatives (Glaxo Laboratories Ltd.). GB633892.
(With I.M. Heilbron) 1-Ethynylcyclohexenes (Glaxo Laboratories Ltd.). GB627453.
(With I.M. Heilbron) 2,5-Dimethylfuran and acetonylacetone. US2470070.
(With K.J. Reed) Cyanines (Imperial Chemical Industries Ltd.). GB616223.
(With I.M. Heilbron) Derivatives of cyclohexene (Glaxo Laboratories Ltd.). US2531567.
(With I.M. Heilbron) Alkynylalkenylcarbinols. US2525672.
(With A.E. Bide, R. J. Nicholls) Esters of 7-halo cholesterol (Glaxo Laboratories, Ltd.). US2531688.
(With M.C. Whiting) -Methylene--lactones. GB640489.
(With M.C. Whiting, H.P.W. Huggill, D.B. Kelly) Glasslike polymers (Imperial Chemical Industries
Ltd.). GB641310.
(With I.K.M. Robson) Methylolpentadecyl phenol and its derivatives (British Resin Products Ltd.).
GB634960.
(With I.M. Heilbron, B.C.L. Weedon, A.B.A. Jansen) 3-Methyl-4,6-octadien-1-yn-3-ol (Glaxo
Laboratories Ltd.). DE818348.
(With I.M. Heilbron, B.C.L. Weedon, B.A. Hems, A.B.A. Jansen) Unsaturated carbinols (Glaxo
Laboratories Ltd.). DE810628.
(With I.M. Heilbron, B.C.L. Weedon, B.A. Hems, A.B.A. Jansen) Vitamin A precursors (Glaxo
Laboratories Ltd.). US2608588.
(With I.M. Heilbron, B.C.L. Weedon, A.B.A. Jansen) Unsaturated carbinols (Glaxo Laboratories
Ltd.). GB674059.
(With I.M. Heilbron, B.C.L. Weedon) 6-Methyl-3,5,7-octatrien-2-one (Glaxo Laboratories Ltd.).
US2606930.
(With I.M. Heilbron, B.C.L. Weedon, B.A. Hems, A.B.A. Jansen) Unsaturated carbinols (Glaxo
Laboratories Ltd.). GB667106.
(With I.M. Heilbron, B.C.L. Weedon) Unsaturated ketones (Glaxo Laboratories Ltd.). GB665146.
Jones 14
(385)
(386)
(387)
1953
1955
(388)
1956
(389)
(390)
(391)
1958
1959
(392)
(393)
1960
1971
(With I.M.Heilbron, B.C.L. Weedon, A.B.A. Jansen) Unsaturated carbinols (Glaxo Laboratories
Ltd.). GB665147.
(With R.M. Evans) Vitamin A synthesis (Glaxo Laboratories Ltd.). GB696235.
(With H.B. Henbest, G.F. Woods, D.E. Hathway, G.H. Thomas) 11-Oxo 9-steroids (Glaxo
Laboratories Ltd.). GB738381.
(With H.B. Henbest, G.F. Woods, D.E. Hathway, G.H. Thomas) 11-Oxo 9-steroids (Glaxo
Laboratories Ltd.). DE944608.
(With H.B. Henbest) 9-Halo-11-oxo-5-steroids (Glaxo Laboratories Ltd.). GB794336.
(With H.B. Henbest) 9-Halo-11-oxo-5-steroids (Glaxo Laboratories Ltd.). US2910471.
(With H.B. Henbest, G.F. Woods, D.E. Hathway, G.H. Thomas) 11-Oxo-9-steroids (Glaxo
Laboratories Ltd.). US2897213.
Halogen-substituted ethynyl carbinols (Beecham Research Laboratories Ltd.). GB836280.
(With G.D. Meakins, A.S. Clegg) Microbiological hydroxylation of steroids (Glaxo Laboratories
Ltd.). DE2116601.
Obituaries and memoirs
(394) 1958
John Lionel Simonsen; Proc. Chem. Soc., 86-89.
(395) 1952
(With L. Bateman) Heinz Peter Koch; J. Chem. Soc., 269.
(396)
Albert Edward Gillam; J. Chem. Soc., 267-268.
(397) 1962
Ian Morris Heilbron; Proc. Chem. Soc., 242-245.
(398) 1973
George Rowntree Ramage; Chemistry in Britain, 364.
(399) 1979
Robert Burns Woodward; Chemistry in Britain, 634.
(400) 1982
(With P. Garratt) Franz Sondheimer; Biog. Memoirs R. Soc., 28, 505-536.
(401) 1983
Alan W. Johnson; Chemistry in Britain, 931-932.
(402) 1984
(With R. Bonnett) Alan Woodworth Johnson; Biog. Memoirs R. Soc., 30, 319- 348.
(403) 1985
Lionel Charles Cross; Chemistry in Britain, 164.
(404) 1989
F. Arnold Robinson; Chemistry in Britain, 69.
(405) 1990
Johnson, Alan Woodworth and Spinks, Alfred; in The Dictionary of National Biography 1981-1985,
Oxford University Press.
(406) 1991
Robert Downs Haworth; Biog. Memoirs R. Soc., 37, 265-276.
Miscellaneous
(407) 1936
(408) 1949
(409) 1953
(410)
1966
(411)
1970
(412)
(413)
(414)
1973
1982
(415)
1984
(416)
(417)
(418)
1989
1992
1998
Synthesis in the sesquiterpene series [PhD thesis, University of Wales].
Professor Sir Ian Heilbron [An appreciation]; Sci. J. Roy. Coll. Sci., 19, 1-8.
(Editor, with A. H. Cook; I. M. Heilbron and H. M. Bunbury were Editors in Chief; T. G. Halsall and
J. R. A. Pollock were Assistant Editors) Dictionary of Organic Compounds, New and Revised Edition
in Four Volumes, Eyre and Spottiswoode.
Industry-University cooperation [An address at the opening of the Unilever Research Laboratory, The
Frythe, Welwyn]; Chem. and Ind., 864-866.
Introduction; to Essays in Free-radical Chemistry [A tribute to D.H. Hey F.R.S. and W.A. Waters
F.R.S.], The Chemical Society.
(With V. Thaller) Microbiological polyacetylenes; in CRC Handbook of Microbiology, 3, 63-74.
Our Society [Presidential Address at the Annual Chemical Congress], Chemistry in Britain, 506-507.
What’s What in Organic Chemistry [A review of Dictionary of Organic Compounds, 5th Edn.];
Nature, 300, 386.
(With V. Thaller) Microbiological polyacetylenes; in CRC Handbook of Microbiology, 2nd Edn., 5,
83-99.
An architect reflects [An essay on CS/RSC publishing activities]; Chemistry in Britain, 111-112.
Early English steroid history; Steroids, 8, 357-362.
The Joneses and Others [Family history]; printed for private circulation.
This bibliography was compiled partly from ERHJ’s personal records and reprint collection, partly from SciFinder
Scholar®, and partly by accidental discovery. Bibliographic searching was somewhat confused by the fact that ERHJ is
credited as E.R. Jones in some early publications, and an Emrys R.H. Jones appears as author of a number of papers in
organic chemistry in the period 1955-1965.
Online searching of the Library of Congress catalogue revealed a video recording of an interview given by ERHJ
which was made under the auspices of ACS in 1992 (LC Centre number 93511064), but no copy of this could be
located in the UK.
No attempt was made to trace the secret wartime reports by ERHJ and colleagues on work undertaken by them,
mostly for the Ministry of Supply, which may survive at the PRO, possibly in classes SUPP23, SUPP28 and/or WO189:
much of this work, which was mostly on the preparation of lachrymatory halocompounds, was declassified and
published after the War in J. Chem. Soc.
Jones 15
Letters to The Times, of which ERHJ wrote several (e.g. 29 September 1986 on PhD career statistics he had
collected) are not included; nor are brief book reviews, or reports of committees and public bodies of which he was
chairman, which he no doubt wrote most of (e.g. Safety in Research, 1983, a report for the Royal Society).
ERHJ’s bound reprint collection (compiled by him) contains over 150 papers on which his name does not appear as
an author, but which (judging by context and the acknowledgements) he made a major contribution to many of and
which perhaps ought to be regarded as output of the Jones school. These papers are not listed above.
Thanks are due Mr Peter Sozanski d’Alancaisez of Balliol College for expert assistance with the manipulation in
Endnote® of data retrieved from SciFinder Scholar®.
Jones 16