硫分解
有机硫化合物
化学
区域选择性
有机化学
戒指(化学)
催化作用
组合化学
硫黄
多酚
原花青素
抗氧化剂
作者
Zhihua Chen,Saeed Mohammadi Nasr,Mosstafa Kazemi,Masoud Mohammadi
出处
期刊:Mini-reviews in Organic Chemistry
[Bentham Science]
日期:2019-07-24
卷期号:17 (4): 352-362
被引量:38
标识
DOI:10.2174/1570193x16666190723111746
摘要
The β-hydroxy sulfides are an important class of organosulfur compounds that have a key role in the synthesis of bioactive compounds containing biological and natural products. The thiolysis of epoxides is the most common and best route for the synthesis of β-hydroxy sulfides. During the last decade, the applications of a diverse range of catalysts and promoter agents in green and organic mediums as well as under solvent-free conditions for the regioselective ring-opening reactions of epoxides with thiols in order to synthesize β-hydroxy sulfides have been studied by various research groups. This review is focused on the important achievements reported in the literature for the thiolysis of epoxides.
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