Preparation of 2,3-dihydrofurans via a double allylic substitution reaction of allylic nitro compounds.

J Org Chem

Department of Applied Molecular Bioscience, Graduate School of Medicine, Yamaguchi University, 2-16-1, Tokiwadai, Ube 755-8611, Japan.

Published: September 2014

A one-step conversion of allylic nitro compounds to substituted 2,3-dihydrofurans has been developed. Allylic nitro compounds, which are readily available from nitroalkenes and formaldehyde, underwent a double allylic substitution reaction catalyzed by a palladium complex to give 2,3-dihydrofurans in good yield.

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http://dx.doi.org/10.1021/jo5013042DOI Listing

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