Trimethylsilyl derivatives as final nucleophiles in the tandem sequence of an ArSCl-initiated AdE reaction resulting in the synthesis of polyfunctional compounds-Reference-Cited by-同舟云学术

Trimethylsilyl derivatives as final nucleophiles in the tandem sequence of an ArSCl-initiated AdE reaction resulting in the synthesis of polyfunctional compounds

Published:1997-01 Issue:2 Volume:7 Page:48-49
ISSN:0959-9436
Container-title:Mendeleev Communications
language:en
Short-container-title:Mendeleev Communications

Author:

Hayford Anthony,Lovdahl Mark,Lazareva Margarita I.,Kryschenko Yury K.,Johnson Tiffany,Dilman Alexander D.,Smoliakova Irina P.,Caple Ron,Smit William A.

Publisher

Elsevier BV

Subject

General Chemistry

Reference9 articles.

1. Stepwise Electrophilic Addition. Some Novel Synthetic Ramifications of an Old Concept

2. A Novel Method of Crossed-Aldol Condensation: Alkylation of Trimethylsilyl Enol Ethers by Alkyl 1-Chloro-2-arylthioalkyl Ethers

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1. ChemInform Abstract: Trimethylsilyl Derivatives as Final Nucleophiles in the Tandem Sequence of an ArSCl-Initiated AdE Reaction Resulting in the Synthesis of Polyfunctional Compounds.;ChemInform;2010-08-03

2. The Use oftert-Butyl Vinyl Ether in Stepwise Electrophilic Addition Reactions;Synthetic Communications;2000-09

3. Reaction of vinyl ethers with ArSCl adducts of d-glucal;Tetrahedron;1999-04

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5. Four-component couplingvia a sequence of threeAd E reactions involving arenesulfenyl chloride, two alkyl vinyl ether units, and silicon-containing π-donors as a method for the synthesis of polyfunctional compounds;Russian Chemical Bulletin;1998-05