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