An Efficient Synthesis of Unsymmetrical Dithioacetals from Sulfoxides and Thiols by the Magnesium Amide-Induced Pummerer-Type Reaction-Reference-Cited by-同舟云学术

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An Efficient Synthesis of Unsymmetrical Dithioacetals from Sulfoxides and Thiols by the Magnesium Amide-Induced Pummerer-Type Reaction

Published:1996-09 Issue:9 Volume:69 Page:2645-2647
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Kobayashi Kazuhiro,Kawakita Masataka,Akamatsu Hideki,Morikawa Osamu,Konishi Hisatoshi

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj/69/9/69_9_2645/_pdf

Reference15 articles.

1. Reactions of Sulfoxides with Magnesium Amides. Transformation of Sulfoxides into Sulfides, Dithioacetals, and Vinyl Sulfides

2. Reductive α-Substitution of Sulfoxides with Grignard Reagents Promoted by a Magnesium Amide

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1. α‐Functionalisation of Cyclic Sulfides Enabled by Lithiation Trapping;Angewandte Chemie International Edition;2023-12-07

2. α‐Functionalisation of Cyclic Sulfides Enabled by Lithiation Trapping;Angewandte Chemie;2023-12-07

3. ChemInform Abstract: An Efficient Synthesis of Unsymmetrical Dithioacetals from Sulfoxides and Thiols by the Magnesium Amide-Induced Pummerer-Type Reaction.;ChemInform;2010-08-04

4. Modern Pummerer-type reactions;Tetrahedron;2006-05

5. Functions Incorporating Two Chalcogens Other Than Oxygen;Comprehensive Organic Functional Group Transformations II;2005

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