期刊
ORGANIC LETTERS
卷 18, 期 20, 页码 5384-5387出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b02762
关键词
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资金
- National Natural Science Foundation of China [21602187, 21572194, 21372187]
- Hunan Provincial Innovative Foundation for Postgraduate [CX2016B260]
- Program for Innovative Research Cultivation Team in University of Ministry of Education of China [1337304]
An efficient indole-to-carbazole strategy has been developed under metal-free conditions. This carbazole formation was highly promoted by NH4I with high regioselectivity through formal [2 + 2 + 2] annulation of indoles, ketones, and nitroolefins. It thus conveniently enabled the assembly of a large number of diversified carbazole products with good tolerance of a broad range of functional groups.
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