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Sulfur-directed carbon–sulfur bond cleavage for Rh-catalyzed regioselective alkynylthiolation of alkynes
Chemical Communications ( IF 4.9 ) Pub Date : 2017-07-21 00:00:00 , DOI: 10.1039/c7cc04997h
Takanori Shibata 1, 2, 3, 4, 5 , Akihito Mitake 1, 2, 3, 4, 5 , Yosuke Akiyama 3, 4, 5, 6, 7 , Kyalo Stephen Kanyiva 3, 4, 5, 8
Affiliation  

Sulfur-directed sp C–S bond cleavage along with a regioselective reaction with alkynes proceeded to give (Z)-enyne sulfides in high to excellent yields. Mechanistic studies were conducted, including characterization of an intermediate. An intramolecular variant realized the construction of a dibenzodithiepin skeleton, which is a seven-membered ring with two sulfur atoms.

中文翻译:

硫定向的碳硫键裂解,用于Rh催化的炔烃区域选择性炔基硫醇化反应

硫定向的sp C–S键断裂以及与炔烃的区域选择性反应继续以高到极好的收率得到(Z)-烯炔硫化物。进行了机理研究,包括中间体的表征。分子内变体实现了二苯并二硫平骨架的构造,该骨架是具有两个硫原子的七元环。
更新日期:2017-07-28
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