Issue 20, 2013

Asymmetric synthesis of trans-dihydroarylfurans in a Friedel–Crafts/substitution domino reaction under squaramide catalysis

Abstract

Dihydroarylfuran skeletons are efficiently synthesized from (Z)-bromonitroalkenes and naphthol derivatives in good yields and excellent enantioselectivities by using squaramide catalysis.

Graphical abstract: Asymmetric synthesis of trans-dihydroarylfurans in a Friedel–Crafts/substitution domino reaction under squaramide catalysis

Supplementary files

Article information

Article type
Communication
Submitted
27 Nov 2012
Accepted
24 Dec 2012
First published
03 Jan 2013

Chem. Commun., 2013,49, 2001-2003

Asymmetric synthesis of trans-dihydroarylfurans in a Friedel–Crafts/substitution domino reaction under squaramide catalysis

C. Jarava-Barrera, F. Esteban, C. Navarro-Ranninger, A. Parra and J. Alemán, Chem. Commun., 2013, 49, 2001 DOI: 10.1039/C2CC38534A

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