ASYMMETRIC ALLYLIC ALKYLATION CATALYZED BY PALLADIUM COMPLEXES WITH NEW CHIRAL LIGANDS

Citation
Gx. Zhu et al., ASYMMETRIC ALLYLIC ALKYLATION CATALYZED BY PALLADIUM COMPLEXES WITH NEW CHIRAL LIGANDS, Tetrahedron letters, 37(26), 1996, pp. 4475-4478
Citations number
44
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404039
Volume
37
Issue
26
Year of publication
1996
Pages
4475 - 4478
Database
ISI
SICI code
0040-4039(1996)37:26<4475:AAACBP>2.0.ZU;2-K
Abstract
A potential chiral tridentate ligand based on 2,6-disubstituted pyridi ne has been prepared and its palladium complexes have been used in asy mmetric allylic alkylation. Up to 75 % ee is achieved in the reaction between 1,3-diphenyl-2-propenyl acetate and dimethyl malonate. A contr ol experiment with a similar ligand without pyridine suggests that the bidentate diphosphine coordination is responsible for the asymmetric reaction with this potential tridentate ligand. Copyright (C) 1996 Els evier Science Ltd