Issue 70, 2020, Issue in Progress

Enantioselective amination of 4-alkylisoquinoline-1,3(2H,4H)-dione derivatives

Abstract

A mild and efficient enantioselective amination of 4-alkylisoquinoline-1,3(2H,4H)-dione derivatives was established, which is compatible with a broad range of substrates and delivers the final products in excellent yields (up to 99%) and ee values (up to 99%) with low catalyst loading (down to 1 mol%). The synthetic potential of this methodology was also demonstrated in the gram scale level.

Graphical abstract: Enantioselective amination of 4-alkylisoquinoline-1,3(2H,4H)-dione derivatives

Supplementary files

Article information

Article type
Paper
Submitted
11 Sep 2020
Accepted
06 Nov 2020
First published
25 Nov 2020
This article is Open Access
Creative Commons BY license

RSC Adv., 2020,10, 42912-42915

Enantioselective amination of 4-alkylisoquinoline-1,3(2H,4H)-dione derivatives

C. Cheng, Y. Li, X. Jia, J. Zhang, Y. Zhao, W. Feng, L. Tang and Y. Yang, RSC Adv., 2020, 10, 42912 DOI: 10.1039/D0RA07806A

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