Issue 5, 2020

Recent advances in phosphine catalysis involving γ-substituted allenoates

Abstract

Organophosphine catalysis of allenoates has doubtlessly been one of the most ideal and powerful synthetic strategies for the generation of highly functionalized carbo-/hetero-cycle motifs, which are important structural motifs in biologically active natural products and pharmaceuticals. Because of their diverse and amazing reactivity, chemists usually pay more attention to the study of 2,3-butadienoates and α-substituted allenoates. More recently, there is a growing interest in the study of phosphine catalysis of γ-substituted allenoates, which usually have low reactivity and selectivity. This feature article will describe the selected examples of organophosphine catalysis of γ-substituted allenoates with a wide range of electrophiles.

Graphical abstract: Recent advances in phosphine catalysis involving γ-substituted allenoates

Article information

Article type
Feature Article
Submitted
21 10月 2019
Accepted
09 12月 2019
First published
10 12月 2019

Chem. Commun., 2020,56, 680-694

Recent advances in phosphine catalysis involving γ-substituted allenoates

E. Li and Y. Huang, Chem. Commun., 2020, 56, 680 DOI: 10.1039/C9CC08241G

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