Recent advances in palladium-catalysed asymmetric 1,4-additions of arylboronic acids to conjugated enones and chromones

Beilstein J Org Chem. 2021 May 10:17:1048-1085. doi: 10.3762/bjoc.17.84. eCollection 2021.

Abstract

The transition metal (palladium)-catalysed asymmetric 1,4-addition of arylboronic acids to conjugated enones belong to the most important and emerging strategies for the construction of C-C bonds in an asymmetric fashion. This review covers known catalytic systems used for this transformation. For clarity, we are using the type of ligand as a sorting criterion. Finally, we attempted to create a flowchart facilitating the selection of a suitable ligand for a given combination of enone and arylboronic acid.

Keywords: Michael addition; Pd complexes; asymmetric reaction; boronic acid; chromones; conjugated enones; enantioselective catalysis.

Publication types

  • Review

Grants and funding

The authors thank the Czech Ministry of Education Youth and Sports (project number SGS_2021_004) for financial support.