Issue 6, 2004

Kinetic resolution of chiral aminoalkenes via asymmetric hydroamination/cyclisation using binaphtholate yttrium complexes

Abstract

Chiral binaphtholate yttrium aryl complexes are highly active and enantioselective catalysts for the asymmetric hydroamination of aminoalkenes, as well as the kinetic resolution of α-substituted 1-aminopent-4-enes to give trans-2,5-disubstituted pyrrolidines with good enantiomeric excess and high krel.

Graphical abstract: Kinetic resolution of chiral aminoalkenes via asymmetric hydroamination/cyclisation using binaphtholate yttrium complexes

Supplementary files

Article information

Article type
Communication
Submitted
11 Dec 2003
Accepted
26 Jan 2004
First published
20 Feb 2004

Chem. Commun., 2004, 730-731

Kinetic resolution of chiral aminoalkenes via asymmetric hydroamination/cyclisation using binaphtholate yttrium complexes

D. V. Gribkov and K. C. Hultzsch, Chem. Commun., 2004, 730 DOI: 10.1039/B316096C

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