Issue 88, 2021

1,1-Diaminoazines as organocatalysts in phospha-Michael addition reactions

Abstract

1,1-Diaminoazines can act as effective organocatalysts for the formation of phosphorus–carbon bonds between biphenylphosphine oxide and an activated alkene (Michael acceptor). These catalysts provide the P–C adducts at a faster rate and with relatively better yields in comparison to the organocatalysts employed earlier. The notable advantage is that 1,1-diaminoazines catalyse the reaction even in an aqueous medium with very good yields. Organocatalysis using 1,1-diaminoazines was also successfully carried out between dimethylphosphite and benzylidenemalononitrile under multicomponent conditions.

Graphical abstract: 1,1-Diaminoazines as organocatalysts in phospha-Michael addition reactions

Supplementary files

Article information

Article type
Communication
Submitted
21 Aug 2021
Accepted
13 Oct 2021
First published
26 Oct 2021

Chem. Commun., 2021,57, 11717-11720

1,1-Diaminoazines as organocatalysts in phospha-Michael addition reactions

A. A. Wani, S. S. Chourasiya, D. Kathuria and P. V. Bharatam, Chem. Commun., 2021, 57, 11717 DOI: 10.1039/D1CC04657H

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