The use of chiral phosphinites in asymmetric chemistry. 3. Enantioselective hydrogenation of α,β-unsaturated carboxylic acids catalyzed by Ru3(CO)12 and glucophinite, idophinite, and camphinite
- 1 September 1980
- journal article
- Published by Elsevier in Journal of Molecular Catalysis
- Vol. 9 (3), 307-311
- https://doi.org/10.1016/0304-5102(80)80020-4
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Chiral phosphinites derived from .alpha.-D-glucofuranose and .alpha.-L-idofuranose. A comparison to chiral phosphines in asymmetric hydrogenationThe Journal of Organic Chemistry, 1980
- Asymmetric chemistry. Comparison of chiral phosphines vs. chiral phosphinites in the asymmetric hydrogenation of prochiral olefins containing a carboxylic acid or ester groupThe Journal of Organic Chemistry, 1979
- Asymmetric chemistry. Alcohol effects upon the (+)-1,2,2-trimethyl-1,3-bis(hydroxymethyl)cyclopentane-lithium aluminum hydride reduction of acetophenoneThe Journal of Organic Chemistry, 1979
- Asymmetric synthesis by chiral ruthenium complexes : II. Enantioselective hydrogenation of α,β-unsaturated carboxylic acids catalyzed by ruthenium complexes containing the ligand ()-diopJournal of Organometallic Chemistry, 1977