Issue 59, 2014

Construction of fused- and spiro-oxa-[n.2.1] skeletons by a tandem epoxide rearrangement/intramolecular [3+2] cycloaddition of cyclopropanes with carbonyls

Abstract

A Lewis acid promoted tandem reaction of epoxide rearrangement and intramolecular [3+2] cycloaddition reaction of cyclopropanes with carbonyls formed by epoxide rearrangement in situ, which were obtained with difficulty by a general method, is reported. A wide variety of fused- and spiro-oxa-[n.2.1] skeletons could be efficiently constructed.

Graphical abstract: Construction of fused- and spiro-oxa-[n.2.1] skeletons by a tandem epoxide rearrangement/intramolecular [3+2] cycloaddition of cyclopropanes with carbonyls

Supplementary files

Article information

Article type
Communication
Submitted
10 Apr 2014
Accepted
05 Jun 2014
First published
13 Jun 2014

Chem. Commun., 2014,50, 8061-8064

Construction of fused- and spiro-oxa-[n.2.1] skeletons by a tandem epoxide rearrangement/intramolecular [3+2] cycloaddition of cyclopropanes with carbonyls

L. Wang, Z. Shi, X. Cao, B. Li and P. An, Chem. Commun., 2014, 50, 8061 DOI: 10.1039/C4CC02641A

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