Asymmetric hydroformylation and hydrogenation catalyzed by chiral rhodium and ruthenium complexes of phosphorylated 2,2 '-bis(diphenyl-phosphino)-1,1'-binaphthyls

Citation
A. Kockritz et al., Asymmetric hydroformylation and hydrogenation catalyzed by chiral rhodium and ruthenium complexes of phosphorylated 2,2 '-bis(diphenyl-phosphino)-1,1'-binaphthyls, J MOL CAT A, 174(1-2), 2001, pp. 119-126
Citations number
41
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
ISSN journal
13811169 → ACNP
Volume
174
Issue
1-2
Year of publication
2001
Pages
119 - 126
Database
ISI
SICI code
1381-1169(20011001)174:1-2<119:AHAHCB>2.0.ZU;2-4
Abstract
In situ-generated rhodium complexes of mono- and bisphosphorylated enantiop ure BINAP ligands have been used for the asymmetric hydroformylation of sty rene and vinylacetate. Corresponding Ru-complexes have been investigated in the homogeneous and biphasic asymmetric hydrogenation of dimethyl itaconat e. An increase in the enantioselectivity of about 6-9% compared to BINAP wa s observed in the vinylacetate hydroformylation. For the aqueous biphasic h ydroformylation of styrene the most enantio selective rhodium diphosphine c atalyst (27% e.e.) up to now has been found. (C) 2001 Elsevier Science B.V. All rights reserved.