Issue 7, 2017

Chiral GAP catalysts of phosphonylated imidazolidinones and their applications in asymmetric Diels–Alder and Friedel–Crafts reactions

Abstract

The design and synthesis of recyclable imidazolidinone catalysts using GAP chemistry/technique was described. Their applications in asymmetric Diels–Alder and Friedel–Crafts reactions with α,β-unsaturated aldehydes resulted in excellent yields and higher enantioselectivities than previous processes. As recyclable small molecular catalysts, phosphonylated imidazolidinones can be recovered and reused for up to three runs without costing significant decrease in catalytic activity.

Graphical abstract: Chiral GAP catalysts of phosphonylated imidazolidinones and their applications in asymmetric Diels–Alder and Friedel–Crafts reactions

Supplementary files

Article information

Article type
Paper
Submitted
24 Dec 2016
Accepted
24 Jan 2017
First published
24 Jan 2017

Org. Biomol. Chem., 2017,15, 1718-1724

Chiral GAP catalysts of phosphonylated imidazolidinones and their applications in asymmetric Diels–Alder and Friedel–Crafts reactions

S. Qiao, J. Mo, C. B. Wilcox, B. Jiang and G. Li, Org. Biomol. Chem., 2017, 15, 1718 DOI: 10.1039/C6OB02801B

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