ASYMMETRIC HYDROFORMYLATION OF STYRENE WITH PTCL2 (ATROPOISOMERIC DIPHOSPHINE) SNCL2 SYSTEMS

Citation
A. Scrivanti et al., ASYMMETRIC HYDROFORMYLATION OF STYRENE WITH PTCL2 (ATROPOISOMERIC DIPHOSPHINE) SNCL2 SYSTEMS, Journal of molecular catalysis. A, Chemical, 101(3), 1995, pp. 217-220
Citations number
19
Categorie Soggetti
Chemistry Physical
ISSN journal
13811169
Volume
101
Issue
3
Year of publication
1995
Pages
217 - 220
Database
ISI
SICI code
1381-1169(1995)101:3<217:AHOSWP>2.0.ZU;2-W
Abstract
The new chiral complex [PtCl2{(S)-(-)-MeOBIPHEP}], where MeOBIPHEP is the atropoisomeric diphosphine 2,2'-bis( diphenylphosphino)-6,6'-dimet hoxy-1,1'-biphenyl, has been synthesized. In the presence of SnCl2 thi s species is an efficient catalyst for the asymmetric hydroformylation of styrene. Asymmetric inductions are higher than those attainable us ing the system [PtCl2{(R)-(+)-BINAP}]/SnCl2, where BINAP is 2,2'-bis(d iphenylphosphino)-1,1'-binaphthyl. The influence of CO and H-2 partial pressures on the catalytic activity of the [PtCl2{(S)-(-)-MeOBIPHEP}] /SnCl2 system has also been studied.