A Cluster-based Catalytic Hydrogenation System with High Conversion and Reversible Enantioselectivity
(2000) In Organometallics 19(26). p.5568-5568- Abstract
- Four tetranuclear ruthenium carbonyl hydrido clusters consisting of the enantiomeric pairs [H4Ru4(CO)10{-1,2-(R/S,R/S)-bdpp}] and [H4Ru4(CO)10{1,1-(R/S,R/S)-bdpp}] containing chiral (R,R)- or (S,S)-bdpp [bdpp = (2R/S,4R/S)-2,4-bis(diphenylphosphino)pentane] have been prepared and fully characterized. These clusters catalyze asymmetric hydrogenation of tiglic acid [trans-2-methyl-2-butenoic acid] with high conversion rates (75-100%) under relatively mild reaction conditions. Enantiomeric excesses of 40-46% were observed; the predominating enantiomeric form of the hydrogenated product is dependent on the configuration of the diphosphine ligand, indicating strong chiral induction.
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/959688
- author
- Homanen, Pertti LU ; Persson, Roger ; Haukka, Matti ; Pakkanen, Tapani and Nordlander, Ebbe LU
- organization
- publishing date
- 2000
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Organometallics
- volume
- 19
- issue
- 26
- pages
- 5568 - 5568
- publisher
- The American Chemical Society (ACS)
- external identifiers
-
- scopus:0034500121
- ISSN
- 1520-6041
- DOI
- 10.1021/om000367c
- language
- English
- LU publication?
- yes
- id
- 2062959a-e0cd-4998-a41a-d4b68c22a70c (old id 959688)
- date added to LUP
- 2016-04-01 12:31:24
- date last changed
- 2022-04-21 08:38:11
@article{2062959a-e0cd-4998-a41a-d4b68c22a70c, abstract = {{Four tetranuclear ruthenium carbonyl hydrido clusters consisting of the enantiomeric pairs [H4Ru4(CO)10{-1,2-(R/S,R/S)-bdpp}] and [H4Ru4(CO)10{1,1-(R/S,R/S)-bdpp}] containing chiral (R,R)- or (S,S)-bdpp [bdpp = (2R/S,4R/S)-2,4-bis(diphenylphosphino)pentane] have been prepared and fully characterized. These clusters catalyze asymmetric hydrogenation of tiglic acid [trans-2-methyl-2-butenoic acid] with high conversion rates (75-100%) under relatively mild reaction conditions. Enantiomeric excesses of 40-46% were observed; the predominating enantiomeric form of the hydrogenated product is dependent on the configuration of the diphosphine ligand, indicating strong chiral induction.}}, author = {{Homanen, Pertti and Persson, Roger and Haukka, Matti and Pakkanen, Tapani and Nordlander, Ebbe}}, issn = {{1520-6041}}, language = {{eng}}, number = {{26}}, pages = {{5568--5568}}, publisher = {{The American Chemical Society (ACS)}}, series = {{Organometallics}}, title = {{A Cluster-based Catalytic Hydrogenation System with High Conversion and Reversible Enantioselectivity}}, url = {{http://dx.doi.org/10.1021/om000367c}}, doi = {{10.1021/om000367c}}, volume = {{19}}, year = {{2000}}, }