Issue 17, 2011

N-Heterocyclic carbene-catalyzed cascade epoxide-opening and lactonization reaction for the synthesis of dihydropyrone derivatives

Abstract

N-Heterocyclic carbene was employed as an efficient organic catalyst to catalyze a cascade epoxide-opening and lactonization reaction. This organocatalytic process could transform various readily accessible γ-epoxy-α,β-enals into dihydropyrone derivatives in good to excellent yields.

Graphical abstract: N-Heterocyclic carbene-catalyzed cascade epoxide-opening and lactonization reaction for the synthesis of dihydropyrone derivatives

Supplementary files

Article information

Article type
Communication
Submitted
30 May 2011
Accepted
24 Jun 2011
First published
24 Jun 2011

Org. Biomol. Chem., 2011,9, 5948-5950

N-Heterocyclic carbene-catalyzed cascade epoxide-opening and lactonization reaction for the synthesis of dihydropyrone derivatives

J. Qi, X. Xie, J. He, L. Zhang, D. Ma and X. She, Org. Biomol. Chem., 2011, 9, 5948 DOI: 10.1039/C1OB05854A

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