Issue 38, 2011

Synthesis of substituted [3]dendralenes and their unique cycloaddition reactions

Abstract

Dimethylsulfonium methylide mediated olefination of 2-phenylethenylidene phosphonoacetate followed by the Horner–Wadsworth–Emmons reaction with aromatic aldehydes provided access to reactive 1,5-diaryl-2-ethoxycarbonyl [3]dendralenes which in situ underwent Diels–Alder cyclodimerisation leading to highly functionalised cyclohexenes with very high regio- and stereoselectivity.

Graphical abstract: Synthesis of substituted [3]dendralenes and their unique cycloaddition reactions

Supplementary files

Article information

Article type
Communication
Submitted
13 Jul 2011
Accepted
15 Aug 2011
First published
26 Aug 2011

Chem. Commun., 2011,47, 10809-10811

Synthesis of substituted [3]dendralenes and their unique cycloaddition reactions

R. Singh and S. K. Ghosh, Chem. Commun., 2011, 47, 10809 DOI: 10.1039/C1CC14211A

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