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Highly enantioselective Ru-catalyzed hydrogenation of β-keto esters using electron-donating bis(trialkylphosphine) ligand-TangPhos
- Source :
-
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry . Mar2006, Vol. 47 Issue 12, p1901-1903. 3p. - Publication Year :
- 2006
-
Abstract
- Abstract: Highly electron-donating bis(trialkylphosphine) TangPhos and its corresponding ruthenium complexes provided high enantioselectivities for the hydrogenation of β-keto esters. Up to 99.8% and 99.5% ee have been achieved in hydrogenation of β-alkyl and β-aryl substituted β-keto esters, respectively. Asymmetric hydrogenation of ethyl 4-chloro acetoacetate in 98.2% ee is also reported. [Copyright &y& Elsevier]
- Subjects :
- *ORGANIC compounds
*HYDROGENATION
*ESTERS
*AMYL acetate
Subjects
Details
- Language :
- English
- ISSN :
- 00404039
- Volume :
- 47
- Issue :
- 12
- Database :
- Academic Search Index
- Journal :
- Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 19768916
- Full Text :
- https://doi.org/10.1016/j.tetlet.2006.01.093