Issue 30, 2016

Synthesis of highly substituted γ-hydroxybutenolides through the annulation of keto acids with alkynes and subsequent hydroxyl transposition

Abstract

An efficient synthesis of highly functionalized γ-hydroxybutenolides through BF3-catalyzed annulation of keto acids with alkynes is described. Many advantages such as the use of routine reagents, easy operation, and a 100% atom efficiency are demonstrated in the method. The reaction can be readily scaled up to gram quantities, offering good practicality.

Graphical abstract: Synthesis of highly substituted γ-hydroxybutenolides through the annulation of keto acids with alkynes and subsequent hydroxyl transposition

Supplementary files

Article information

Article type
Communication
Submitted
20 Feb 2016
Accepted
16 Mar 2016
First published
16 Mar 2016

Chem. Commun., 2016,52, 5269-5272

Synthesis of highly substituted γ-hydroxybutenolides through the annulation of keto acids with alkynes and subsequent hydroxyl transposition

W. Mao and C. Zhu, Chem. Commun., 2016, 52, 5269 DOI: 10.1039/C6CC01554A

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