[2,3] Sigmatropic Rearrangement of Unstable Sulfur Ylides from Allyl Sulfonium Salts. Comparative Study of Electrochemical Reduction with the Base Method and Mechanism Elucidation by the MO Method-Reference-Cited by-同舟云学术

[2,3] Sigmatropic Rearrangement of Unstable Sulfur Ylides from Allyl Sulfonium Salts. Comparative Study of Electrochemical Reduction with the Base Method and Mechanism Elucidation by the MO Method

Published:2004-09 Issue:9 Volume:77 Page:1687-1695
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Okazaki Yuichi,Ando Fumio,Koketsu Jugo

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference17 articles.

1. Studies on the action of 2,3-epoxysqualene-sterol cyclase on unnatural substrates produced by alkylidene transfer from sulfonium alkylides to 4,8,13,17,21-pentamethyldocosa-4,8,12,16,20-pentaenal

2. Azabicyclobutanes. Synthesis of 3-phenyl-1-azabicyclo[1.1.0]butane

3. Dimethyloxosulfonium Methylide ((CH3)2SOCH2) and Dimethylsulfonium Methylide ((CH3)2SCH2). Formation and Application to Organic Synthesis

4. Studies of Acenaphthene Derivatives. XX. The Reactions of Benzylideneacenaphthenones with Sulfonium Ylides

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