ESKANDARKOLVARI PAGE 1/4
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Aug. 2011
CONTACT INFORMATION
Name:Eskandar Kolvari
Address:Department of Chemistry, Faculty of Science, SemnanUniversity, Seman, P.O. Box35195-363.
Phone: 0098 - 231- 3354100
Fax:0098 - 231- 3354082
Email: and
PERSONAL INFORMATION
Date of Birth:20March 1977
Place of Birth:Garmsar
Citizenship:Iran
Marital Status:Married,
POSTION: Assistant Professor.
EDUCATION:
2004-2009Ph.D.: Chemistry
Field: Organic Chemistry
Title:Application of solid acids and nano tube like reagents in organic synthesis
Faculty of Chemistry, Bu-AliSinaUniversity, Hamedan, I.R. Iran.
2000-2003 M.Sc.: Chemistry
Field: Organic Chemistry
Faculty of Chemistry, Bu-AliSinaUniversity, Hamedan, I.R. Iran
1995-2000 B. Sc.: Chemistry
Field: Applied Chemistry
Department of Chemistry;SharifUniversity of Technology, Tehran, I.R. Iran.
TEACHING EXPERIENCE (Nov., 1996-up to now)
Graduate
/ UndergraduateHeterocyclic Chemistry
New Topics in Organic Chemsitry
Reactive Intermediates / 1. Organic Chemistry I, II & III
2. Medicinal Chemistry,
3. General Chemistry,
4. Organic Chemistry Lab.
CURRENT RESEARCH INTERESTS:
Green and new methodology in Organic Chemsitry
MEMBERSHIP:
Iranian Chemical Society
REFEREED JOURNAL PAPERS[1-19]
2011------
1.Kolvari, E.; Zolfigol, M. A.; Peiravi, M. Green synthesis of quinoxaline derivatives using p-dodecylbenzensulfonic acid as a surfactant-type Bronsted acid catalyst in water. Green Chemistry Letters & Reviews2011,Accepted.
2.Kolvari, E.; Zolfigol, M. A.; Koukabi, N.; Shirmardi-Shaghasemi, B. A Simple and Efficient One-Pot Synthesis Of Hantzsch 1,4-Dihydropyridines Using Silica Sulfuric Acid as A Heterogeneous and Reusable Catalyst under Solvent-Free Conditions. Chemical Papers2011,Accepted.
3.Kolvari, E.; Zolfigol, M. A.; Banary, H. Surfactant-Assisted Synthesis of Bis(Indolyl)Methanes in Water. Chinese Chemical Letters2011,Accepted.
4.Kolvari, E.; Khazaei, A.; Zolfigol, M. A.; Koukabi, N.; Gilandoust, M.; Bakhit, N. Rapid and highly efficient trimethylsilylation of alcohols and phenols with hexamethyldisilazane (HMDS) catalyzed by in-situ generated I2 Using Oxone®/KI or cerium ammonium nitrate (CAN)/KI systems under mild conditions. Journal of Chemical Sciences2011,Accepted.
5.Zolfigol, M. A.; Kolvari, E.; Koukabi, N.; Salehzadeh, S.; Chehardoli, G.; Tidmarsh, I. S.; Niknam, K. 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 Society2011,8, 484-494.
6.Zolfigol, M. A.; Khazaei, A.; Kolvari, E.; Koukabi, N.; Gilandoust, M. New Reagent for the One-Step Synthesis of gem-Chloronitro Compounds from Oximes. Journal of Iranian Chemical Society2011,Accepted.
7.Koukabi, N.; Kolvari, E.; Khazaei, A.; Zolfigol, M. A.; Shirmardi-Shaghasemi, B.; Khavasi, H. R. Hantzsch reaction on free nano-Fe2O3 catalyst: excellent reactivity combined with facile catalyst recovery and recyclability. Chemical Communications2011,47, 9230-9232.
2010------
8.Zolfigol, M. A.; Kolvari, E.; Abdoli, A.; Shiri, M. Synthesis of new tripodal Hantzsch 1,4-dihydropyridines under solvent-free condition and their conversion to the corresponding tripodal pyridines. Molecular Diversity2010,14, 809-813.
9.Zolfigol, M. A.; Khazaei, A.; Kolvari, E.; Koukabi, N.; Soltani, H.; Behjunia, M. H(5)IO(6)/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 Acta2010,93, 587-594.
10.Khazaei, A.; Zolfigol, M. A.; Kolvari, E.; Koukabi, N.; Soltani, H.; Bayani, L. S. Electrophilic Bromination of Alkenes, Alkynes, and Aromatic Amines with Iodic Acid/Potassium Bromide Under Mild Conditions. Synthetic Communications2010,40, 2954-2962.
2009------
11.Zolfigol, M. A.; Khazaei, A.; Kolvari, E.; Koukabi, N.; Soltani, H.; Behjunia, M.; Khakyzadeh, V. HIO(3)/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. Arkivoc2009, 200-210.
12.Khazaei, A.; Zolfigol, M. A.; Kolvari, E.; Koukabi, N.; Soltani, H.; Komaki, F. Electrophilic Bromination of Alkenes, Alkynes, and Aromatic Amines with Potassium Bromide/Orthoperiodic Acid under Mild Conditions. Synthesis-Stuttgart2009, 3672-3676.
2008------
13.Zolfigol, M. A.; Salehi, P.; Shiri, M.; Sayadi, A.; Abdoli, A.; Keypour, H.; Rezaeivala, M.; Niknam, K.; Kolvari, E. A simple and efficient route for the synthesis of di and tri(bis(indolyl) methanes) as new triarylmethanes. Molecular Diversity2008,12, 203-207.
2007------
14.Zolfigol, M. A.; Shirini, F.; Chehardoli, G.; Kolvari, E. A catalytic and transition metal-free method for the chemoselective oxidation of alcohols to their corresponding carbonyl compounds using periodic acid or iodic acid in the presence of a catalytic amount of KBr. Journal of Molecular Catalysis a-Chemical2007,265, 272-275.
15.Zolfigol, M. A.; Niknam, K.; Bagherzadeh, M.; Ghorbani-Choghamarani, A.; Koukabi, N.; Hajjami, M.; Kolvari, E. Tribromoisocyanuric acid (TBCA) and Oxonee (R)-MX systems as oxidizing agents: Oxidative coupling of thiols to their corresponding disulfides under mild and heterogeneous conditions. Journal of the Chinese Chemical Society2007,54, 1115-1118.
16.Zolfigol, M. A.; Bagherzadeh, M.; Mallakpour, S.; Chehardoli, G.; Kolvari, E.; Choghamarani, A. G.; Koukabi, N. 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 Communications2007,8, 256-260.
17.Kolvari, E.; Ghorbani-Choghamarani, A.; Salehi, P.; Shirini, F.; Zolfigol, M. A. Application of N-halo reagents in organic synthesis. Journal of the Iranian Chemical Society2007,4, 126-174.
2006------
18.Kolvari, E. Sodium hydrogen sulfate: Safe and efficient. Synlett2006, 1971-1972.
2004------
19.Khazaei, A.; Mallakpour, S.; Zolfigol, M. A.; Ghorbani-Vaghei, R.; Kolvari, E. The application of N,N '-dibromo-N,N '-1,2-ethanediyl bis(P-toluenesulfonamide) as a powerful reagent for conversion of carboxylic acids into esters and amides with triphenylphosphine. Phosphorus Sulfur and Silicon and the Related Elements2004,179, 1715-1721.
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