SYNTHESIS, DETERMINATION OF ENANTIOMERIC PURITY AND STRUCTURAL CHARACTERIZATION OF ENANTIOPURE (2R,5R)-(-2,5-BIS-(DIPHENYLPHOSPHINO)-HEXANE, A CHIRAL DPPB ANALOG())

Citation
C. Wiesauer et al., SYNTHESIS, DETERMINATION OF ENANTIOMERIC PURITY AND STRUCTURAL CHARACTERIZATION OF ENANTIOPURE (2R,5R)-(-2,5-BIS-(DIPHENYLPHOSPHINO)-HEXANE, A CHIRAL DPPB ANALOG()), Tetrahedron : asymmetry, 7(2), 1996, pp. 397-398
Citations number
11
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear","Chemistry Physical
Journal title
ISSN journal
09574166
Volume
7
Issue
2
Year of publication
1996
Pages
397 - 398
Database
ISI
SICI code
0957-4166(1996)7:2<397:SDOEPA>2.0.ZU;2-M
Abstract
Enantiopure (2R,5R)-(+)-2,5-bis-(diphenylphosphino)hexane, 3, a chiral analogue of 1,4-bis-(diphenylphosphino)butane was synthesized in two steps from enantiomerically pure (2S,5S)-(+)-hexanediol. The molecular structure of (2R,5R)-3 was determined by X-ray structure analysis of its nickel-(II)-complex showing a rare dimeric species; NMR analysis o f the reaction product of 3 with {2-[1-(dimethylamino)ethyl]phenyl-C,N }-dipalladium allowed to deduce the enantiomeric purity.