Citation: Abdukader Ablimita, Zhang Yonghong, Zhang Zengpeng, Liu Chenjiang. Recent Advances of the Access to Indolinones via C—H Bond Functionalization/Cyclization Cascade Strategy[J]. Chinese Journal of Organic Chemistry, ;2016, 36(5): 875-888. doi: 10.6023/cjoc201601013 shu

Recent Advances of the Access to Indolinones via C—H Bond Functionalization/Cyclization Cascade Strategy

a.
School of Chemistry and Chemical Engineering, Xinjiang University, Urumqi 830046
b.
Physics and Chemistry Detecting Center, Xinjiang University, Urumqi 830046

Corresponding author: Liu Chenjiang, pxylcj@126.com
Received Date: 12 January 2016
Revised Date: 28 March 2016

Fund Project: Project supported by the National Natural Science Foundation of China Nos. 21572195, 21562039, 21502162

Figures(30)

Due to the diverse biological activities of indolinones, especially 3,3-disubstituted indolinones, their researches of synthesis have been attracting considerable interest in the areas of organic chemistry. Recently, the radical addition and cyclization reaction of N-arylacrylamides with different radical precursors for the efficient construction of indolinones motifs have attracted much attention. This review summarizes the recent advances of the access to 3,3-disubstituted indolinones based on C—H bond functionalization/cyclization cascade strategy. These reaction mechanisms have also been introduced.
- C—H functionalization,
- oxindoles,
- cascade reaction
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