期刊
MOLECULES
卷 25, 期 23, 页码 -出版社
MDPI
DOI: 10.3390/molecules25235595
关键词
indol; indole-3-carboxylates; indole-3-carboxyamides; 3-aroylindoles; 3-acylindoles; N-oxyenamines; [3; 3]-sigmatropic rearrangement; annulation; DABCO; organocatalysis
资金
- Spanish Ministry of Science, Innovation and Universities (MICINN) [PGC2018-094503-B-C21]
- State Research Agency (AEI) [PGC2018-094503-B-C21]
- European Regional Development Funds (ERDF) [PGC2018-094503-B-C21]
A consecutive 2-step synthesis of N-unprotected polysubstituted indoles bearing an electron-withdrawing group at the C-3 position from readily available nitroarenes is reported. The protocol is based on the [3,3]-sigmatropic rearrangement of N-oxyenamines generated by the DABCO-catalyzed reaction of N-arylhydroxylamines and conjugated terminal alkynes, and delivers indoles endowed with a wide array of substitution patterns and topologies.
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