Synthetic Communications®

Facile and efficient Michael addition of indole to nitroolefins catalyzed by Zn (OAc) 2· 2H2O

X Ji, H Tong, Y Yuan

Index: Ji, Xiang; Tong, Haibo; Yuan, Yu Synthetic Communications, 2011 , vol. 41, # 3 p. 372 - 379

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Citation Number: 8

Abstract

View all references ] The 3-position of indole is one of the building blocks for biologically active compounds. Addition of indole to nitroolefins fulfills the synthesis of 3-substituted indole. Traditionally the Michael addition of indole to nitroalkenes is catalyzed by a strong base and Brønsted acid. [ 3 3. (a) Hiemstra , H. ; Wiberg , H. Addition of aromatic thiols to conjugated cycloalkenones, catalyzed by chiral β-hydroxy amines: A mechanistic study of ...