Heterocyclization approach for electrooxidative coupling of functional primary alkylamines with aromatics

T Morofuji, A Shimizu, J Yoshida

Index: Morofuji, Tatsuya; Shimizu, Akihiro; Yoshida, Jun-Ichi Journal of the American Chemical Society, 2014 , vol. 136, # 12 p. 4496 - 4499

Full Text: HTML

Citation Number: 11

Abstract

A new approach for electrooxidative coupling of aromatic compounds and primary alkylamines bearing a functional group such as a hydroxyl group and an amino group was developed. The key to the success of the transformation is heterocyclization of functional primary alkylamines. Treatment of primary alkylamines bearing a functional group with nitriles or their equivalents gives the corresponding heterocycles. The electrochemical ...

Related Articles:

Copper (II) hydroxide complexes of N-heterocyclic carbenes and catalytic oxidative amination of arylboronic acids

[Liu, Bo; Liu, Bin; Zhou, Yongbo; Chen, Wanzhi Organometallics, 2010 , vol. 29, # 6 p. 1457 - 1464]

Catalyst??Free N??Arylation Using Unactivated Fluorobenzenes

[Diness, Frederik; Fairlie, David P. Angewandte Chemie - International Edition, 2012 , vol. 51, # 32 p. 8012 - 8016]

Photophysical processes of some benzimidazole derivatives

[Chen, Zhaobin; Zhang, Caihong; Feng, Liheng Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, 2005 , vol. 62, # 1-3 p. 592 - 595]

More Articles...