Issue 6, 2017

Efficient synthesis of multiply substituted butenolides from keto acids and terminal alkynes promoted by combined acids

Abstract

A general, efficient, and operationally simple approach to highly substituted butenolides through the annulation of keto acids and terminal alkynes is described. This reaction is promoted by the combination of Lewis and Brønsted acids, furnishing a variety of butenolides in synthetically useful yields.

Graphical abstract: Efficient synthesis of multiply substituted butenolides from keto acids and terminal alkynes promoted by combined acids

Supplementary files

Article information

Article type
Research Article
Submitted
16 Dec 2016
Accepted
13 Feb 2017
First published
14 Feb 2017

Org. Chem. Front., 2017,4, 1029-1033

Efficient synthesis of multiply substituted butenolides from keto acids and terminal alkynes promoted by combined acids

W. Mao and C. Zhu, Org. Chem. Front., 2017, 4, 1029 DOI: 10.1039/C6QO00820H

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