Synthesis 2002(1): 0031-0033
DOI: 10.1055/s-2002-19303
SHORTPAPER
© Georg Thieme Verlag Stuttgart · New York

Mixed Cyano-Gilman Cuprates - Advances in Conjugate Addition to α,β-Unsaturated Pyroglutaminol

Lennart Bunch, Povl Krogsgaard-Larsen, Ulf Madsen*
Department of Medicinal Chemistry, The Royal Danish School of Pharmacy, Universitetsparken 2, DK-2100 Copenhagen, Denmark
Fax: +45(35)306040; e-Mail: um@dfh.dk;
Further Information

Publication History

Received 10 August 2001
Publication Date:
04 August 2004 (online)

Abstract

Conjugate addition of lower order cuprates to protected α,β-unsaturated pyroglutaminol 1 is of limited value, mainly due to the requirement for a large excess of the transferable ligand (10 equiv). Here we report advances using mixed cyano-Gilman cuprates which allow the use of only 1.2 equiv of the transferable ligand, to give the desired product in acceptable to good yield (68-84%). Diethyl ether as the solvent was found advantageous versus THF, since the use of TMSCl could be avoided.

12

The chemical purity of the commercially available trans-2-trimethylsilylvinylbromide was estimated to be approximately 85%.