7459-69-0Relevant articles and documents
An efficient and straightforward approach for accessing thionoesters: Via palladium-catalyzed C-N cleavage of thioamides
Liu, Yinbo,Mo, Xiaofeng,Majeed, Irfan,Zhang, Mei,Wang, Hui,Zeng, Zhuo
supporting information, p. 1532 - 1537 (2022/03/01)
We report for the first time the coupling of activated thioamides with alcohols to efficiently form thionoesters via a palladium-catalyzed C-N cleavage strategy. The new approach employs thioamides as a thioacylating reagent to give thionoesters in moderate to good yields. Notably, this methodology demonstrates a broad substrate scope, as alkyl/aryl alcohols are well tolerated, and this process might facilitate the synthesis of sulfur-containing compounds under simple and mild conditions. This journal is
A general and efficient route to thionoesters via thionoacyl nitrobenzotriazoles
Shalaby, M. Ashraf,Rapoport, Henry
, p. 1065 - 1070 (2007/10/03)
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