- 著者
-
新井 和孝
- 出版者
- The Society of Synthetic Organic Chemistry, Japan
- 雑誌
- 有機合成化学協会誌 (ISSN:00379980)
- 巻号頁・発行日
- vol.39, no.5, pp.374-384, 1981-05-01 (Released:2009-11-13)
- 参考文献数
- 70
- 被引用文献数
-
5
6
In recent years, α-chlorosulfides have been utilized as very useful synthetic intermedites. Firstly, in this article, the preparation methods of α-chlorosulfides are reviewed, and the critical points of the preparative reactions are summerized as follows : (1) selectivity of degree of the chlorination, (2) α, β-elimination of hydrogen chloride, (3) cleavage of C-S bond of sulfides, and (4) regioselectivity of the chlorination. Secondly, many types of the reaction of α-chlorosulfides are introduced together with each typical application in organic synthesis, classified in three groups, (1) the reactions with nucleophiles, (2) the reactions as electrophiles, and (3) miscellaneous reactions.The scope and limitation of the synthetic utility of the reaction of α-chlorosulfides will be clarified in this review.