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Direct C(sp3)–H acyloxylation of indolin-3-ones with carboxylic acids catalysed by KI†
Yong-Long Zhao,Yong-Qin Tang,Xing-Hai Fei,Fen-Fen Yang,Zhuo-Xian Cao,Dong-Zhu Duan,Qing-Jie Zhao,Yuan-Yong Yang,Meng Zhou,Bin He
Green Chemistry Pub Date : 03/04/2020 00:00:00 , DOI:10.1039/C9GC04446A
Abstract

The first KI-catalyzed direct acyloxylation of indolin-3-ones with carboxylic acids has been developed using 30% aq. H2O2 as a green oxidant at room temperature. Through this strategy, various C2-acyloxy indolin-3-ones were obtained in up to 96% yield. Moreover, the C2-acyloxy indolin-3-ones can serve as versatile intermediates for the synthesis of nucleophilic 2-monoarylated indolin-3-ones and 3-ylidene indoles.

Graphical abstract: Direct C(sp3)–H acyloxylation of indolin-3-ones with carboxylic acids catalysed by KI
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