化学
分子内力
硫代氨基甲酸酯类
钯
芳基
催化作用
电泳剂
药物化学
组合化学
氧化磷酸化
立体化学
有机化学
生物化学
烷基
作者
Yingwei Zhao,Yinjun Xie,Chungu Xia,Hanmin Huang
标识
DOI:10.1002/adsc.201400306
摘要
Abstract A palladium‐catalyzed intramolecular CH bond sulfuration reaction of aryl thiocarbamates has been developed. This strategy provides a new route to benzo[ d ][1,3]oxathiol‐2‐ones with tolerance of a wide range of substituents. Mechanistic studies suggested that the CH activation–sulfuration to afford 2‐imino‐1,3‐benzoxathiole intermediate might involve an electrophilic palladation process. magnified image
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