A New Catalytic System for the Hydroformylation of Styrene Using Alkene Complexes of Platinum(0)
✍ Scribed by Carlo Botteghi; Stefano Paganelli; Ugo Matteoli; Alberto Scrivanti; Rocco Ciorciaro; Luigi M. Venanzi
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- German
- Weight
- 196 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The platinum(0) complexes [Pt(C~2~H~4~)(PP)] (PP = 1,2‐bis[(diphenylphosphino)methyl]benzene (2) and (+)‐DIOP = (+)‐1,4‐bis(diphenylphosphino)‐1,4‐dideoxy‐2,3‐O‐isopropyliden‐D‐threitol), when promoted by CH~3~SO~3~H, become active catalysts for styrene hydroformylation with total yields of aldehydes ranging from 44 to 67% und selectivities towards 3‐phenylpropanal ranging from 80 to 88%. Smaller amounts of the corresponding alcohols (3–18%) are also obtained with a selectivity towards 3‐phenylpropanol of 94–96%. When DIOP complexes were used, no stereoselectivity for asymmetric hydroformylation was observed.
📜 SIMILAR VOLUMES
The new mixed phosphane-phosphite ligands 1 and 2, derived from 3,3Ј-di-tert-butyl-2,2Ј-dihydroxy-5,5Ј-dimethoxybiphenyl and (S)-binaphthol, respectively, reacted with [Rh(COD)(THF) 2 ]CF 3 SO 3 to give the compounds [Rh(COD)(1)]CF 3 SO 3 and [Rh(COD)(2)]CF 3 SO 3 in which the ligands 1 and (S)-2 ar