期刊
ADVANCED SYNTHESIS & CATALYSIS
卷 364, 期 1, 页码 64-70出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.202100882
关键词
Rh(III)-catalyzed; C-H allylation; C-H prenylation; C4-selective functionalization; branched allyl indoles
资金
- Guangdong Pharmaceutical University [51377002]
- National Natural Science Foundation of China [22001044]
- Youth Innovation Talents Project of Colleges and Universities in Guangdong Province [51377201, 51340208]
In this study, Rh(III)-catalyzed C-H allylation and prenylation of indoles using a weak carbonyl coordination directing group have been reported, providing various allylated and prenylated indoles in moderate to satisfied yields. These reactions demonstrate high functional-groups compatibility and broad substrate scope, making them potentially valuable in organic synthesis. Scale-up experiments and mechanistic studies were also conducted to further investigate this transformation.
Herein, Rh(III)-catalyzed C4-selective C-H allylation and prenylation of indoles by using a weak carbonyl coordination directing group have been reported. By employing 5-methylene-1,3-dioxan-2-ones, 4-vinyl-1,3-dioxolan-2-ones and 2-methyl-2,3-butadiene as scalable cross-coupling partners, these divergent synthesis protocols proceed smoothly under redox-neutral reaction conditions, delivering various allylated and prenylated indoles in moderate to satisfied yields. This transformation exhibits high functional-groups compatibility and broad substrate scope. Scale-up experiment and mechanistic studies were also accomplished.
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