NADIA KOUKABI
‫دث‬
CONTACT INFORMATION
Name: Nadiya Koukabi
Address: Department of Chemistry, Semnan University, Seman, P.O. Box 35195-363.
Phone: 0098 - 231- 3366196
Fax: 0098 - 231- 3354058
Email: n.koukabi@gmail.com, n.koukabi@semnan.ac.ir
EDUCATION:
2006-2010 Ph.D.: Chemistry
Field: Organic Chemistry
Faculty of Chemistry, Bu-Ali Sina University, Hamedan, I.R. Iran.
2004-2006 M.Sc.: Chemistry
Field: Organic Chemistry
Faculty of Chemistry, Bu-Ali Sina University, Hamedan, I.R. Iran
2000-2004 B. Sc.: Chemistry
Field: Pure Chemistry
Department of Chemistry; Islamic Azad University of Firouzabad
Firouzabad, I.R. Iran.
CURRENT RESEARCH INTERESTS:
Application of ionic liquids and nanocatalyst such as
nanomagnetic particles in the synthesis of organic compounds
MEMBERSHIP:
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Iranian Chemical Society
PUBLISHED JOURNAL PAPERS
[1] J. Yousefi-Seyf, K. Tajeian, E. Kolvari, N. Koukabi, A. Khazaei, M.A. Zolfigol, A Green Protocol for the
Bromination and Iodination of the Aromatic Compounds using H5IO6/NaBr and H5IO6/NaI in the
Water, Bull. Korean Chem. Soc, 33 (2012) 2619.
[2] N. Koukabi, E. Kolvari, M.A. Zolfigol, A. Khazaei, B.S. Shaghasemi, B. Fasahati, A Magnetic Particle
Supported Sulfonic Acid Catalyst: Tuning Catalytic Activity between Homogeneous and Heterogeneous
Catalysis, Advanced Synthesis & Catalysis, 354 (2012) 2001-2008.
[3] N. Koukabi, E. Kolvari, M. Zolfigol, A. Khazaei, B. Shaghasemi, B. Fasahati, Hantzsch Reaction with γFe2O3 Nanoparticles Supported Sulfonic Acid, Synfacts, 8 (2012) 1156-1156.
[4] E. Kolvari, A. Khazaei, M.A. Zolfigol, N. Koukabi, M. Gilandoust, N. Bakhit, Rapid and highly efficient
trimethylsilylation of alcohols and phenols with hexamethyldisilazane (HMDS) catalysed by in situ
generated I 2 using Oxone®/KI or cerium ammonium nitrate (CAN)/KI systems under mild conditions,
Journal of Chemical Sciences, (2012) 1-6.
[5] A. Khazaei, M.A. Zolfigol, E. Kolvari, N. Koukabi, M. Gilandoust, Ultrasound Promoted One-Pot
Synthesis of gem-Chloronitro Compounds from Oximes, Organic Preparations and Procedures
International, 44 (2012) 375-380.
[6] M. Zolfigol, E. Kolvari, N. Koukabi, S. Salehzadeh, G. Chehardoli, I. Tidmarsh, K. Niknam, A new
crystal engineering approach for the synthesis of {[K. 18-Crown-6] I 3} n as a nanotube-Like and
recyclable catalyst for the chemoselective silylation of alcohols, Journal of the Iranian Chemical
Society, 8 (2011) 484-494.
[7] M. Zolfigol, A. Khazaei, E. Kolvari, N. Koukabi, M. Gilandoust, New reagent for a one-step synthesis of
gem-chloronitro compounds from oximes, Journal of the Iranian Chemical Society, 8 (2011) 10581062.
[8] N. Koukabi, E. Kolvari, A. Khazaei, M.A. Zolfigol, B. Shirmardi-Shaghasemi, H.R. Khavasi, Hantzsch
reaction on free nano-Fe2O3 catalyst: excellent reactivity combined with facile catalyst recovery and
recyclability, Chemical Communications, 47 (2011) 9230-9232.
[9] E. Kolvari, M.A. Zolfigol, N. Koukabi, B. Shirmardi-Shaghasemi, A simple and efficient one-pot
synthesis of Hantzsch 1, 4-dihydropyridines using silica sulphuric acid as a heterogeneous and reusable
catalyst under solvent-free conditions, Chemical Papers, 65 (2011) 898-902.
[10] M.A. Zolfigol, A. Khazaei, E. Kolvari, N. Koukabi, H. Soltani, M. Behjunia, H 5IO6/KI: A New
Combination Reagent for Iodination of Aromatic Amines, and Trimethylsilylation of Alcohols and
Phenols through in situ Generation of Iodine under Mild Conditions, Helvetica Chimica Acta, 93 (2010)
587-594.
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[11] A. Khazaei, M.A. Zolfigol, E. Kolvari, N. Koukabi, H. Soltani, F. Komaki, Electrophilic Bromination of
Alkenes, Alkynes, and Aromatic Amines with Potassium Bromide/Orthoperiodic Acid under Mild
Conditions, ChemInform, 41 (2010) no-no.
[12] A. Khazaei, M.A. Zolfigol, E. Kolvari, N. Koukabi, H. Soltani, L.S. Bayani, Electrophilic bromination of
alkenes, alkynes, and aromatic amines with iodic acid/potassium bromide under mild conditions,
Synthetic Communications®, 40 (2010) 2954-2962.
[13] M.A. Zolfigol, A. Khazaei, E. Kolvari, N. Koukabi, H. Soltani, M. Behjunia, V. Khakyzadeha, HIO3/KI:
A new combination reagent for iodination of aromatic amines and trimethylsilylation of alcohols and
phenols through in situ generation of iodine under mild conditions, Arkivoc, 13 (2009) 200-210.
[14] M.A. Zolfigol, K. Niknam, M. Bagherzadeh, A. Ghorbani-Choghamarani, N. Koukabi, M. Hajjami, E.
Kolvari, Tribromoisocyanuric Acid (TBCA) and Oxone®-MX Systems as Oxidizing Agents: Oxidative
Coupling of Thiols to their Corresponding Disulfides under Mild and Heterogeneous Conditions,
JOURNAL-CHINESE CHEMICAL SOCIETY TAIPEI, 54 (2007) 1115.
[15] M.A. Zolfigol, M. Bagherzadeh, S. Mallakpour, G. Chehardoli, E. Kolvari, A.G. Choghamarani, N.
Koukabi, Mild and heterogeneous oxidation of urazoles to their corresponding triazolinediones via in
situ generation Cl+ using silica sulfuric acid/KClO3 or silica chloride/oxone system, Catalysis
Communications, 8 (2007) 256-260.
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