A computational study on the reaction mechanism and energetics of Markovnikov and anti-Markovnikov addition in alkyne hydrothiolation reactions-Reference-Cited by-同舟云学术

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A computational study on the reaction mechanism and energetics of Markovnikov and anti-Markovnikov addition in alkyne hydrothiolation reactions

Published:2016-12 Issue: Volume:1098 Page:13-21
ISSN:2210-271X
Container-title:Computational and Theoretical Chemistry
language:en
Short-container-title:Computational and Theoretical Chemistry

Author:

Jayasree Elambalassery G.,Reshma Sobhana

Funder

Department of Science and Technology – Science and Engineering Research Board

Kerala State Council for Science, Technology and Environment

Publisher

Elsevier BV

Subject

Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry

Reference30 articles.

1. Stereoselective formation of Z- or E-vinyl thioethers from arylthiols and acetylenes under transition-metal-free conditions;Liao;Eur. J. Org. Chem.,2013

2. The emergence of transition-metal-mediated hydrothiolation of unsaturated carbon-carbon bonds: a mechanistic outlook;Castarlenas;Angew. Chemie - Int. Ed.,2013

3. Alkyne hydrothiolation catalyzed by a dichlorobis(aminophosphine) complex of palladium: selective formation of cis-configured vinyl thioethers;Gerber;Chem. - A Eur. J.,2012

4. Addition of SH bonds across electron-deficient olefins catalyzed by well-defined copper(I) thiolate complexes;Delp;Inorg. Chem.,2007

5. Highly stereoselective anti-Markovnikov hydrothiolation of alkynes and electron-deficient alkenes by a supported Cu-NHC complex;Yang;Green Chem.,2014

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4. Computationally unraveling the mechanism and selectivity of five and six membered N‐heterocyclic carbene‐catalyzed alkyne hydrochalcogenation;International Journal of Quantum Chemistry;2021-03-10

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