Issue 76, 2020

Asymmetric acyl-Mannich reaction of isoquinolines with α-(diazomethyl)phosphonate and diazoacetate catalyzed by chiral Brønsted acids

Abstract

An efficient asymmetric acyl-Mannich reaction of isoquinolines with α-(diazomethyl)phosphonate and diazoacetate has been developed using chiral spiro phosphoric acids as catalysts. This reaction allowed the construction of a series of chiral 1,2-dihydroisoquinolines bearing a tertiary stereocenter at the C1 position with up to 98% yield and 99% ee.

Graphical abstract: Asymmetric acyl-Mannich reaction of isoquinolines with α-(diazomethyl)phosphonate and diazoacetate catalyzed by chiral Brønsted acids

Supplementary files

Article information

Article type
Communication
Submitted
04 May 2020
Accepted
13 Aug 2020
First published
18 Aug 2020

Chem. Commun., 2020,56, 11235-11238

Asymmetric acyl-Mannich reaction of isoquinolines with α-(diazomethyl)phosphonate and diazoacetate catalyzed by chiral Brønsted acids

W. Wu, Y. Wang, J. Guo, L. Cai, Y. Chen, Y. Huang and Y. Peng, Chem. Commun., 2020, 56, 11235 DOI: 10.1039/D0CC03201H

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