General synthetic route to chiral flexible biphenylphosphine ligands: The use of a chiral additive enables the preparation and observation of metal complexes incorporating the enantiopure form

Citation
K. Mikami et al., General synthetic route to chiral flexible biphenylphosphine ligands: The use of a chiral additive enables the preparation and observation of metal complexes incorporating the enantiopure form, ORG LETT, 3(2), 2001, pp. 243-245
Citations number
25
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANIC LETTERS
ISSN journal
15237060 → ACNP
Volume
3
Issue
2
Year of publication
2001
Pages
243 - 245
Database
ISI
SICI code
1523-7060(20010125)3:2<243:GSRTCF>2.0.ZU;2-L
Abstract
[GRAPHICS] The enantio- and diastereomerically pure metal complex of a chirally flexib le BIPHEP ligand is obtained through enantiomer-selective coordination of a BIPHEP-RU complex with enantiopure 3,3'-dimethyldiaminobinaphthyl, DM-DBN, followed by epimerization of the remaining BIPHEP-RU enantiomer to complex with DM-DABN. Thus, an efficient and general synthetic route to a variety of substituted BIPHEP ligands from biphenol and observation of the enantiom erically pure BIPHEP ligands in their Ru(II) complexes are described.