Site and Stereoselectivity of the Cyclopropanation of Unsymmetrically Substituted 1,3-Dienes by the Simmonssmith Reaction.+-Reference-Cited by-同舟云学术

Site and Stereoselectivity of the Cyclopropanation of Unsymmetrically Substituted 1,3-Dienes by the Simmonssmith Reaction.+

Published:1996-05 Issue:9 Volume:26 Page:1793-1800
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Guerreiro Mário César,Schuchardt Ulf

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/00397919608002620

Reference12 articles.

1. Simmons, H. E., Cairns, T. L., Vladuchick, S. A. and Hoiness, C. M. 1973.Organic Reactions, Edited by: Dauben, W. G. Vol. v 20, 1–131. New York: John Wiley & Sons.

2. The Role of the Activator for Zinc in the Simmons-Smith Reaction. A Convenient General Procedure

3. Photochemistry of .alpha.,.beta.-unsaturated esters. IV. Cyclopropyl conjugation in olefinic esters. Conformational effects on ultraviolet absorption

4. Notizen: Eine Synthese der DL- Chrysanthemumsäure

5. Monomers and Polymers, A Synthesis of Vinyl Cyclopropane and Dicyclopropyl1

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5. Regio- and stereoselective cyclopropanation of functionalised dienes. Novel methodology for the synthesis of vinyl- and divinyl-cyclopropanes;Tetrahedron Letters;2002-03