Theoretical Study of Nucleophilic Substitution at Two-Coordinate Sulfur-Reference-Cited by-同舟云学术

Theoretical Study of Nucleophilic Substitution at Two-Coordinate Sulfur

Published:2001-02-15 Issue:6 Volume:66 Page:2005-2010
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Bachrach Steven M.¹,Gailbreath BettyCep D.¹

Affiliation:

1. Department of Chemistry, Trinity University, 715 Stadium Drive, San Antonio, Texas 78212, and Department of Chemistry, Northern Illinois University, DeKalb, Illinois 60115

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo001463q

Reference27 articles.

1. Nucleophilic substitution at dicoordinated sulfur. Effect of the leaving group on the reaction between triphenylmethyl sulfenyl derivatives and butylamine

2. Formation of an intermediate in nucleophilic substitution at dicoordinated sulfur

3. The relative nucleophilicity of some common nucleophiles toward sulfinyl sulfur. The nucleophile-catalyzed hydrolysis of aryl sulfinyl sulfones

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