Issue 2, 2009

Synthesis and evaluation of guanidinyl pyrrolidines as bifunctional catalysts for enantioselective conjugate additions to cyclic enones

Abstract

Guanidinyl pyrrolidines derived from ‘S’-proline are effective catalysts for the enantioselective conjugate addition of malonate, nitroalkane and other carbon and heteroatom nucleophiles to cyclohexenone and cyclopentenone in the absence of basic additives. The stereoselectivity is strongly dependant on catalyst loading as well as reaction concentration.

Graphical abstract: Synthesis and evaluation of guanidinyl pyrrolidines as bifunctional catalysts for enantioselective conjugate additions to cyclic enones

Supplementary files

Article information

Article type
Paper
Submitted
14 Jul 2008
Accepted
19 Sep 2008
First published
17 Nov 2008

Org. Biomol. Chem., 2009,7, 319-324

Synthesis and evaluation of guanidinyl pyrrolidines as bifunctional catalysts for enantioselective conjugate additions to cyclic enones

S. V. Pansare and R. Lingampally, Org. Biomol. Chem., 2009, 7, 319 DOI: 10.1039/B812038B

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