Generation of a substituted 1,2,4-thiadiazole ring via the [3+2] cycloaddition reaction of benzonitrile sulfide toward trichloroacetonitrile. A DFT study of the regioselectivity and of the molecular mechanism-Reference-Cited by-同舟云学术

Generation of a substituted 1,2,4-thiadiazole ring via the [3+2] cycloaddition reaction of benzonitrile sulfide toward trichloroacetonitrile. A DFT study of the regioselectivity and of the molecular mechanism

Published:2015-12 Issue:12 Volume:18 Page:1277-1283
ISSN:1631-0748
Container-title:Comptes Rendus Chimie
language:en
Short-container-title:Comptes Rendus Chimie

Author:

Emamian Saeedreza

Publisher

Elsevier BV

Subject

General Chemical Engineering,General Chemistry

Reference64 articles.

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2. Mechanism and regioselectivity of the 1,3-dipolar cycloaddition of thiocarbonyl S-imide with cyclopent-3-ene-1,2-dione and methoxyethene: a density functional theory approach

3. Mechanism and regioselectivity of 1,3-dipolar cycloaddition reactions of sulphur-centred dipoles with furan-2,3-dione: A theoretical study using DFT

4. Can the high reactivity of azomethine betaines in [3 + 2] cycloaddition reactions be explained using singlet-diradical character descriptors? What molecular mechanism is actually involved in these cycloadditions?

5. A DFT analysis of the participation of zwitterionic TACs in polar [3+2] cycloaddition reactions

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