Acid Catalyzed Alcoholysis of Sulfinamides: Unusual Stereochemistry, Kinetics and a Question of Mechanism Involving Sulfurane Intermediates and Their Pseudorotation-Reference-Cited by-同舟云学术

Acid Catalyzed Alcoholysis of Sulfinamides: Unusual Stereochemistry, Kinetics and a Question of Mechanism Involving Sulfurane Intermediates and Their Pseudorotation

Published:2015-02-11 Issue:2 Volume:20 Page:2949-2972
ISSN:1420-3049
Container-title:Molecules
language:en
Short-container-title:Molecules

Author:

Bujnicki Bogdan,Drabowicz Józef,Mikołajczyk Marian

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

Link

http://www.mdpi.com/1420-3049/20/2/2949/pdf

Reference33 articles.

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2. High-coordinated Sulfur Compounds;Drabowicz,1993

3. Hypervalent Sulfuranes as Transient and Isolable Structures: Occurence, Synthesis and Reactivity;Drabowicz,1999

4. Stereochemical aspect of the chemistry of hypervalent chalcogen compounds;Drabowicz;Rev. Heteroatom Chem.,2000

5. Recent advances in spirochalcogenurane stereochemistry—A mini review

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