Indole-to-Carbazole Strategy for the Synthesis of Substituted Carbazoles under Metal-Free Conditions
01 natural sciences
0104 chemical sciences
DOI:
10.1021/acs.orglett.6b02762
Publication Date:
2016-10-10T11:15:01Z
AUTHORS (5)
ABSTRACT
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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