Issue 12, 2021

Highly diastereoselective synthesis of vicinal diamines via a Rh-catalyzed three-component reaction of diazo compounds with diarylmethanimines and ketimines

Abstract

A Rh-catalyzed diastereoselective three-component reaction of diazo compounds with diarylmethanimines and ketimines has been reported that offers an efficient and convenient access to vicinal diamine derivatives with two tertiary stereocenters in high yields (75%–>95%) with high to excellent diastereoselectivities. Moreover, the generated product could be easily converted to free diamines via hydrolysis of the imine motif under mild conditions.

Graphical abstract: Highly diastereoselective synthesis of vicinal diamines via a Rh-catalyzed three-component reaction of diazo compounds with diarylmethanimines and ketimines

Supplementary files

Article information

Article type
Research Article
Submitted
16 Jan 2021
Accepted
30 Mar 2021
First published
01 Apr 2021

Org. Chem. Front., 2021,8, 2997-3003

Highly diastereoselective synthesis of vicinal diamines via a Rh-catalyzed three-component reaction of diazo compounds with diarylmethanimines and ketimines

K. Zhou, M. Bao, H. Sha, G. Dong, K. Hong, X. Xu and W. Hu, Org. Chem. Front., 2021, 8, 2997 DOI: 10.1039/D1QO00083G

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