Mohammad Ali Zolfigol
Bu-Ali Sina University
832 Papers
6.8K Citations
Mohammad Ali Zolfigol is an academic researcher from Bu-Ali Sina University. The author has contributed to research in topics: Catalysis & Chemistry. The author has an hindex of 56, co-authored 765 publications. Previous affiliations of Mohammad Ali Zolfigol include Razi University & Payame Noor University.
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Papers
NaBrO3/NaHSO4×H2O as a Versatile Reagent System for the Oxidation of Benzylic Alcohols and Aldehydes.
TL;DR: In this paper, the authors showed that the oxidation of benzylic alcohols and aldehydes by NaBrO3 is efficiently promoted in the presence of NaHSO4·H2O.
Efficient Cleavage of Carbon—Nitrogen Double Bonds under Solvent‐Free Conditions.
TL;DR: In this article, the conversion of oximes, hydrazones and semicarbazones into the corresponding carbonyl compounds is obtained conveniently using (NH4)2Cr2O7 in the presence of ZrCl4 and wet SiO2 under solvent free conditions.
H5IO6/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.
Mohammad Ali Zolfigol,Ardeshir Khazaei,Eskandar Kolvari,Nadiya Koukabi,Hamid Soltani,Maryam Behjunia +5 more
TL;DR: In this paper, a simple method for the in situ generation of iodine using H5IO6/KI has been developed, and its application in silylation of OH group and iodination of aromatic amines is described.
Oxidation of Alcohols Using (NH4)2Cr2O4 in the Presence of Al(HSO4)3 and Wet SiO2.
TL;DR: In this article, a mild and efficient method for the oxidation of alcohols by ammonium dichromate in the presence of Al(HSO4)3 and wet SiO2 in solution or under solvent-free conditions is reported.
Efficient Trimethylsilylation and Tetrahydropyranylation of Alcohols in the Presence of 1,3‐Dibromo‐5,5‐dimethylhydantoin.
TL;DR: In this article, a trimethylsilylation and tetrahydropyranylation of benzylic and primary and secondary aliphatic alcohols proceed efficiently in the presence of 1,3-dibromo-5,5-dimethylhydantoin (DBH) under mild and completely heterogeneous reaction conditions in excellent yields.