M
Mohsen Rostamizadeh
Researcher at University of Sistan and Baluchestan
Publications - 25
Citations - 379
Mohsen Rostamizadeh is an academic researcher from University of Sistan and Baluchestan. The author has contributed to research in topics: Catalysis & Heterogeneous catalysis. The author has an hindex of 10, co-authored 25 publications receiving 361 citations.
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Journal ArticleDOI
Dynamic 1H NMR spectroscopic study of the restricted SN rotation in aryl-N-(arylsulfonyl)-N-(triphenylphosphoranylidene)imidocarbamates
Ali Reza Modarresi-Alam,Ferydoon Khamooshi,Mohsen Rostamizadeh,Hossein Keykha,Mahmoud Nasrollahzadeh,Hamid Reza Bijanzadeh,Erich Kleinpeter +6 more
TL;DR: In this article, aryl-N-(arylsulfonyl)-N-(triphenylphosphoranylidene)imidocarbamates in CDCl3, CD3COCD3, and CD3OD at the temperature range of 183-298
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An efficient synthesis of 2,2′-arylmethylene bis(3-hydroxy-5,5-dimethyl-2-cyclohexene-1-one) and 1,8-dioxooctahydroxanthenes using ZnO and ZnO–acetyl chloride
Malek Taher Maghsoodlou,Sayyed Mostafa Habibi-Khorassani,Zahra Shahkarami,Nariman Maleki,Mohsen Rostamizadeh +4 more
TL;DR: In the presence of ZnO-acetyl chloride catalysts the reaction was limited to give only 1,8-dioxo-octahydroxanthenes 3a-k in very good yields.
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An efficient synthesis of α‐Amino phosphonates using silica sulfuric acid as a heterogeneous catalyst
Malek Taher Maghsoodlou,Sayyed Mostafa Habibi Khorassani,Nourollah Hazeri,Mohsen Rostamizadeh,Seyed Sajad Sajadikhah,Zahra Shahkarami,Nariman Maleki +6 more
TL;DR: In this paper, α-Amino phosphonates were obtained in a one-pot, simple, and efficient method from the reaction between aldehyde, aniline, trialkyl phosphite, and silica sulfuric acid as a catalyst in acetonitrile at room temperature.
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Dynamic 1H NMR study of the barrier to rotation about the C-N bond in primary carbamates and its solvent dependence.
Ali Reza Modarresi-Alam,Parisa Najafi,Mohsen Rostamizadeh,Hossein Keykha,Hamid-Reza Bijanzadeh,Erich Kleinpeter +5 more
TL;DR: The dynamic 1H NMR study of some primary carbamates in the solvents CDCl3 and CD3COCD3 between 183 and 298 K is reported, finding barriers to rotation show solvent dependence in contrast to the tertiary analogues and are lower in free energy.
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Highly stereoselective construction of functionalized cyclopropanes from the reaction between acetylenic esters and C–H acids in the presence of triphenylarsine
Malek Taher Maghsoodlou,Sayyed Mostafa Habibi Khorassani,Reza Heydari,Faramarz Rostami Charati,Nourollah Hazeri,Mojtaba Lashkari,Mohsen Rostamizadeh,Ghasem Marandi,Alexandre N. Sobolev,Mohamed Makha +9 more
TL;DR: In this article, a one-pot triphenylarsine-catalyzed synthesis of transcyclopropane derivatives is achieved by means of the reaction between acetylenic esters and C-H acids in the presence of triphenymine.