Issue 14, 2021

Recent advances of chromone-based reactants in the catalytic asymmetric domino annulation reaction

Abstract

Chiral polycyclic chromanones are important heterocyclic frameworks that constitute the core structures of many natural products and bioactive molecules. As starting materials, the chromone-based reactants are very efficient building blocks in the synthesis of these scaffolds, which could be achieved in one step via catalytic asymmetric annulation reactions and is difficult to duplicate with other strategies. In this review, the catalytic asymmetric domino annulation of polycyclic chromanones is summarized and classified according to the types of chromone-based reactants for the first time. Both organocatalysis and metallic organocatalysis of the asymmetric domino annulation reaction were described along with the catalytic mechanisms and related transformations.

Graphical abstract: Recent advances of chromone-based reactants in the catalytic asymmetric domino annulation reaction

Article information

Article type
Review Article
Submitted
15 Feb 2021
Accepted
09 Apr 2021
First published
14 Apr 2021

Org. Chem. Front., 2021,8, 3968-3989

Recent advances of chromone-based reactants in the catalytic asymmetric domino annulation reaction

M. Zhang, Y. Gong, W. Zhou, Y. Zhou and X. Liu, Org. Chem. Front., 2021, 8, 3968 DOI: 10.1039/D1QO00269D

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements