Clauson–Kaas-type synthesis of pyrrolyl-phenols, from the hydrochlorides of aminophenols, in the presence of nicotinamide

M Chatzopoulou, E Kotsampasakou…

Index: Chatzopoulou, Maria; Kotsampasakou, Eleni; Demopoulos, Vassilis J. Synthetic Communications, 2013 , vol. 43, # 21 p. 2949 - 2954

Full Text: HTML

Citation Number: 4

Abstract

A facile Clauson–Kaas-type pyrrolyl-phenol synthesis has been achieved in the presence of nicotinamide, which is inexpensive and nontoxic. The starting material is aminophenol hydrochloride. This is advantageous in certain cases because it is the only isolatable form of the corresponding aminophenol. ... [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications® for the following free ...

Related Articles:

Copper-catalysed N-arylation of pyrrole with aryl iodides under ligand-free conditions

[Liu, Lili; Wu, Fengtian; Liu, Yan; Xie, Jianwei; Dai, Bin; Zhou, Zhuoqiang Journal of Chemical Research, 2014 , vol. 38, # 3 p. 180 - 182]

Highly efficient and reusable copper-catalyzed N-arylation of nitrogen-containing heterocycles with aryl halides

[Kim, A. Young; Lee, Hyun Ju; Park, Ji Chan; Kang, Hyunju; Yang, Haesik; Song, Hyunjoon; Park, Kang Hyun Molecules, 2009 , vol. 14, # 12 p. 5169 - 5178]

Copper MOF: scope and limitation in catalytic hydroxylation and nitration of aryl halides

[Priyadarshini; Amal Joseph; Kantam, M. Lakshmi; Sreedhar Tetrahedron, 2013 , vol. 69, # 31 p. 6409 - 6414]

Novel approach for the synthesis of N-substituted pyrroles starting directly from nitro compounds in water

[Synthetic Communications, , vol. 42, # 4 p. 548 - 553]

More Articles...