烯丙基重排
化学
区域选择性
催化作用
亲核细胞
有机化学
基质(水族馆)
反应条件
硫黄
组合化学
海洋学
地质学
作者
Zhen Luo,Zheng‐Qiang Liu,Tingting Yang,Xin Zhuang,Chuan‐Ming Hong,Fei-Fei Zou,Zhi-Yong Xue,Qinghua Li,Tang‐Lin Liu
出处
期刊:Organic Letters
[American Chemical Society]
日期:2022-01-06
卷期号:24 (2): 741-745
被引量:17
标识
DOI:10.1021/acs.orglett.1c04206
摘要
A highly regioselective and catalyst-free sulfonation of allylic alcohols with sulfinyl amides has been realized. Such a mix-and-go procedure provides a convenient approach to synthetically various allylic sulfones under mild reaction conditions. Furthermore, this novel reaction shows ample substrate scope and outstanding functional group tolerance and could also be scaled-up. Meanwhile, it is the first example that sulfinyl amides act as a powerful sulfur nucleophile in the reactions. 1,1,1,3,3,3-Hexafluoro-2-propanol (HFIP) as a solvent plays a critical role in allylic sulfonation.
科研通智能强力驱动
Strongly Powered by AbleSci AI