Issue 86, 2013

Palladium-catalyzed insertion of α,β-unsaturated N-tosylhydrazones and trapping with carbon nucleophiles

Abstract

Palladium-catalyzed carbene migratory insertion–cyclization reactions were reported, delivering dihydronaphthalene and indene derivatives in moderate to good yields. A three-component cross-coupling was also developed. The reactions are easy to handle, under mild conditions and various functional groups are tolerated.

Graphical abstract: Palladium-catalyzed insertion of α,β-unsaturated N-tosylhydrazones and trapping with carbon nucleophiles

Supplementary files

Article information

Article type
Communication
Submitted
23 Jul 2013
Accepted
27 Aug 2013
First published
28 Aug 2013

Chem. Commun., 2013,49, 10190-10192

Palladium-catalyzed insertion of α,β-unsaturated N-tosylhydrazones and trapping with carbon nucleophiles

Y. Ye, P. Zhou, J. Luo, M. Zhong and Y. Liang, Chem. Commun., 2013, 49, 10190 DOI: 10.1039/C3CC45583A

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