Open AccessCyanuric Chloride‐Catalyzed Michael Addition of Indoles to Nitroolefins under Solvent‐Free Conditions
Author(s) -
Xiao Juan Yang,
Yun Jing
Publication year - 2012
Publication title -
journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.436
H-Index - 50
eISSN - 2090-9063
pISSN - 2090-9071
DOI - 10.1155/2013/429235
Subject(s) - cyanuric chloride , chemistry , michael reaction , catalysis , solvent , organic chemistry , chloride
Cyanuric chloride is an inexpensive, efficient, and mild catalyst for the Michael addition of indoles to nitroolefins at 70°C under solvent-free conditions. The simple experimental procedure, solvent-free reaction conditions, utilization of an inexpensive and readily available catalyst, short period of conversion, and excellent yields are the advantages of the present method
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