期刊
ORGANIC LETTERS
卷 12, 期 17, 页码 3736-3739出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol101130e
关键词
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资金
- NIH NCRR [P20 RR15569]
- Arkansas Bioscience Institute
A general method for the synthesis of 2,3-disubstituted indoles is described. The key feature of this method is the amination of aromatic C-H bonds via FeCl2-catalyzed ring opening of 2H-azirines. The method tolerates a variety of functional groups such as Br, F, NO2, OMe, CF3, OTBS, alkenes, and OPiv. The method can also be extended to synthesize azaindoles.
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