Issue 9, 2014

Imino exchange reaction in a dearomatization strategy: synthesis of N-acyl diarylamines and phenothiazines from two anilines

Abstract

N-Sulfonyl cyclohexadienimines generated from an iodine(III)-induced oxidative dearomatization of N-sulfonyl protected para-substituted anilines are ready to undergo an imino exchange reaction with another aniline, which provides an alternative way to access N-acyl diarylamines and phenothiazines.

Graphical abstract: Imino exchange reaction in a dearomatization strategy: synthesis of N-acyl diarylamines and phenothiazines from two anilines

Supplementary files

Article information

Article type
Research Article
Submitted
18 Jul 2014
Accepted
14 Aug 2014
First published
18 Aug 2014

Org. Chem. Front., 2014,1, 1055-1057

Author version available

Imino exchange reaction in a dearomatization strategy: synthesis of N-acyl diarylamines and phenothiazines from two anilines

L. Zhang, H. Wang, B. Yang and R. Fan, Org. Chem. Front., 2014, 1, 1055 DOI: 10.1039/C4QO00201F

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