Issue 71, 2014

A convergent rhodium-catalysed asymmetric synthesis of tetrahydroquinolines

Abstract

Rh-catalysed conjugate additions of 2-aminophenyl boronic acid derivatives were exploited in diastereoselective and asymmetric syntheses of tetrahydroquinolines. In both cases, combinatorial variation of the substitution of the tetrahydroquinoline ring system was possible.

Graphical abstract: A convergent rhodium-catalysed asymmetric synthesis of tetrahydroquinolines

Supplementary files

Article information

Article type
Communication
Submitted
27 Jūn. 2014
Accepted
18 Jūl. 2014
First published
23 Jūl. 2014
This article is Open Access
Creative Commons BY license

Chem. Commun., 2014,50, 10222-10224

Author version available

A convergent rhodium-catalysed asymmetric synthesis of tetrahydroquinolines

H. Y. Li, J. Horn, A. Campbell, D. House, A. Nelson and S. P. Marsden, Chem. Commun., 2014, 50, 10222 DOI: 10.1039/C4CC04940C

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