SYNTHESIS OF NEW CHIRAL PHOSPHINEPHOSPHITES HAVING 2-DIPHENYLPHOSPHINOBIPHENYL-2'-YL BACKBONE AND THEIR USE IN RH(I)-CATALYZED ASYMMETRIC HYDROFORMYLATIONS

Citation
T. Higashizima et al., SYNTHESIS OF NEW CHIRAL PHOSPHINEPHOSPHITES HAVING 2-DIPHENYLPHOSPHINOBIPHENYL-2'-YL BACKBONE AND THEIR USE IN RH(I)-CATALYZED ASYMMETRIC HYDROFORMYLATIONS, Tetrahedron letters, 35(13), 1994, pp. 2023-2026
Citations number
4
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404039
Volume
35
Issue
13
Year of publication
1994
Pages
2023 - 2026
Database
ISI
SICI code
0040-4039(1994)35:13<2023:SONCPH>2.0.ZU;2-2
Abstract
New chiral phosphinephosphites l-2'-yl)((S)-1,1'-binaphthalen-2,2'-diy l)phosphite [abbreviated (R,S)-BIPHEMPHOS] and its enantiomer (S,R)-BI PHEMPHOS have been synthesized from '-dichloro-4,4',6,6'-tetramethyl-2 ,2'-biphenyldiol in enantiomerically pure form. Their Rh(I) complexes have been shown to be highly efficient catalysts for asymmetric hydrof ormylations of a variety of olefinic substrates. The corresponding pho sphinephosphites derived from 2,2'-biphenyldiol were also tested as li gands for asymmetric hydroformylation.