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Samiran Halder

Researcher at University of Calcutta

Publications -  5
Citations -  151

Samiran Halder is an academic researcher from University of Calcutta. The author has contributed to research in topics: Glycal & Catalysis. The author has an hindex of 3, co-authored 5 publications receiving 144 citations.

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Journal ArticleDOI

Generation of Nitrile Oxides under Nanometer Micelles Built in Neutral Aqueous Media: Synthesis of Novel Glycal-Based Chiral Synthons and Optically Pure 2,8-Dioxabicyclo[4.4.0]decene Core

TL;DR: A highly efficient strategy for chemoselective oxidation of aldoximes to nitrile oxides by iodosobenzene in neutral aqueous media is reported.
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Synthesis of glycal-based chiral benzimidazoles by VO(acac)2-CeCl3 combo catalyst and their self-aggregated nanostructured materials.

TL;DR: Theoretical calculation by the B3LYP/6-31G** level of theory of the glycal-based chiral benzimidazoles shows out of planar geometry of the 1H-anthra[1,2-d]imidrazole-6,11-dione moiety, which is responsible for the strong self-aggregation to generate ultralong nanostructured materials.
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PhIO as a powerful cyclizing reagent: regiospecific [3+2]-tandem oxidative cyclization of imine toward cofacially self-aggregated low molecular mass organic materials.

TL;DR: The powerful cyclization and tandem oxidation property of environmentally benign PhIO is developed for the first time, which leads to regiospecific [3+2]-tandem oxidative cyclization of imine at room temperature in rapid access to a new class of compounds, 1,2-functionalized 4,5-diarylimidazoles, in excellent yield with synthetic efficiency.
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PhIO as a Powerful Cyclizing Reagent: Regiospecific [3 + 2]‐Tandem Oxidative Cyclization of Imine Toward Cofacially Self‐Aggregated Low Molecular Mass Organic Materials.

TL;DR: In this paper, the powerful cyclization and tandem oxidation property of environmentally benign PhIO is developed for the first time, which leads to regiospecific [3+2]-tandem oxidative cyclization of imine at room temperature in rapid access to a new class of compounds, 1,2-functionalized 4,5-diarylimidazoles, in excellent yield with synthetic efficiency.
Journal ArticleDOI

Synthesis of Glycal-Based Chiral Benzimidazoles by VO(acac)2—CeCl3 Combo Catalyst and Their Self-Aggregated Nanostructured Materials.

TL;DR: In this article, an operationally simple protocol for the synthesis of a wide range of chiral benzimidazoles in high yields without formation of undesired 1,2-disubstituted and pseudoglycal byproducts is presented.