当前位置: X-MOL 学术Chin. J. Chem. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Dehydroxylative Trifluoromethylthiolation, Trifluoromethylation, and Difluoromethylation of Alcohols
Chinese Journal of Chemistry ( IF 5.4 ) Pub Date : 2019-12-25 , DOI: 10.1002/cjoc.201900364
Wei Zhang 1 , Jin‐Hong Lin 1 , Wenfeng Wu 2 , Yu‐Cai Cao 3 , Ji‐Chang Xiao 1
Affiliation  

CF3S, CF3 and HCF2 groups have been identified as valuable functionalities for drug development. Despite significant accomplishments in the trifluoromethylthiolation, trifluoromethylation and difluoromethylation reactions, directly converting common functional groups into CF3S, CF3 or HCF2 groups is still highly desirable. Described here is the dehydroxylative trifluoromethylthiolation, trifluoromethylation and difluoromethylation of alcohols promoted by a R3P/ICH2CH2I system. All of these dehydroxylative reactions were achieved under mild conditions via the activation of the hydroxyl group by the R3P/ICH2CH2I system. A wide substrate scope and good functional group tolerance were observed.

中文翻译:

醇的脱羟基三氟甲基硫醇化,三氟甲基化和二氟甲基化

CF 3 S,CF 3和HCF 2基团已被确定为药物开发的有价值的功能。尽管在三氟甲基硫醇化,三氟甲基化和二氟甲基化反应方面取得了重大成就,仍然非常需要将常见的官能团直接转化为CF 3 S,CF 3或HCF 2基团。在此描述的是由R 3 P / ICH 2 CH 2 I体系促进的醇的脱羟基三氟甲基硫醇化,三氟甲基化和二氟甲基化。所有这些脱羟基反应都是在温和条件下通过R活化羟基而实现的3 P / ICH 2 CH 2 I系统。观察到较宽的底物范围和良好的官能团耐受性。
更新日期:2019-12-26
down
wechat
bug