Note on the Direct α-Phenylsulfenylation of Enolates Generated During 1, 4-Addition Reactions on α, β-Unsaturated Ketones-Reference-Cited by-同舟云学术

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Note on the Direct α-Phenylsulfenylation of Enolates Generated During 1, 4-Addition Reactions on α, β-Unsaturated Ketones

Published:2010-09-01 Issue:4 Volume:86 Page:329-330
ISSN:0037-9646
Container-title:Bulletin des Sociétés Chimiques Belges
language:en
Short-container-title:Bull. Soc. Chim. Belges

Author:

Samson M.,De Wilde H.,Vandewalle M.

Publisher

Wiley

Subject

General Chemistry

Reference13 articles.

1. A review has recently appeared on the regiospecific generation of enolate anions;J. d'Angelo, Tetrahedron,1976

2. New synthetic reactions. Sulfenylation-dehydrosulfenylation as a method for introduction of unsaturation

3. New synthetic reactions. Sulfenylations and dehydrosulfenylations of esters and ketones

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A convergent carbohydrate approach to the synthesis of taxol. Part 1. Ring A subunit;Tetrahedron Letters;1995-04

2. Organocopper Reagents: Substitution, Conjugate Addition, Carbo/Metallocupration, and Other Reactions;Organic Reactions;1992-04-08

3. Nucleophilic Addition–Electrophilic Coupling with a Carbanion Intermediate;Comprehensive Organic Synthesis;1991

4. Tandem Vicinal Difunctionalization: β-Addition to α,β-Unsaturated Carbonyl Substrates Followed by α-Functionalization;Organic Reactions;1990-04-05

5. S-Cyanosilylenolethers: Preparation and Potential Intermediates in Synthesis;Synthetic Communications;1978-01

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