Issue 72, 2016

Enantioselective synthesis of quaternary α-aminophosphonates by Pd-catalyzed arylation of cyclic α-ketiminophosphonates with arylboronic acids

Abstract

A highly enantioselective addition of arylboronic acids to cyclic α-ketiminophosphonates is reported using a chiral palladium phosphinooxazoline catalyst, providing an efficient and facile route to quaternary α-aminophosphonates in high yields and up to 99.9% enantioselectivity.

Graphical abstract: Enantioselective synthesis of quaternary α-aminophosphonates by Pd-catalyzed arylation of cyclic α-ketiminophosphonates with arylboronic acids

Supplementary files

Article information

Article type
Communication
Submitted
16 May 2016
Accepted
08 Aug 2016
First published
09 Aug 2016

Chem. Commun., 2016,52, 10882-10885

Enantioselective synthesis of quaternary α-aminophosphonates by Pd-catalyzed arylation of cyclic α-ketiminophosphonates with arylboronic acids

Z. Yan, B. Wu, X. Gao and Y. Zhou, Chem. Commun., 2016, 52, 10882 DOI: 10.1039/C6CC04096A

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