Issue 6, 2014

Tandem synthesis of 3-allyl-chromones from alkynones and allylic alcohols under metal-free conditions

Abstract

A novel and efficient approach to 3-allyl-chromones from alkynones and allylic alcohols via a tandem Michael addition–Claisen rearrangement–O-arylation reaction has been developed. Diversely structural 3-allyl-chromones were afforded in up to 93% yield for 24 examples. This synthetic strategy is regiospecific, highly efficient, environment friendly and metal-free.

Graphical abstract: Tandem synthesis of 3-allyl-chromones from alkynones and allylic alcohols under metal-free conditions

Supplementary files

Article information

Article type
Communication
Submitted
29 Oct 2013
Accepted
05 Nov 2013
First published
05 Nov 2013

Chem. Commun., 2014,50, 652-654

Tandem synthesis of 3-allyl-chromones from alkynones and allylic alcohols under metal-free conditions

X. Wang, G. Cheng and X. Cui, Chem. Commun., 2014, 50, 652 DOI: 10.1039/C3CC48259F

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