Highly Enantioselective Rh-Catalyzed Hydrogenations with a New Chiral 1,4-Bisphosphine Containing a Cyclic Backbone
- 1 February 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 119 (7) , 1799-1800
- https://doi.org/10.1021/ja9634381
Abstract
No abstract availableThis publication has 27 references indexed in Scilit:
- BINAP: an efficient chiral element for asymmetric catalysisAccounts of Chemical Research, 1990
- Chiral Metal Complexes as Discriminating Molecular CatalystsScience, 1990
- Enantioselective Synthesis with Optically Active Transition-Metal CatalystsSynthesis, 1988
- Asymmetric hydrogenationAccounts of Chemical Research, 1983
- Asymmetric synthesis. Asymmetric catalytic hydrogenation using chiral chelating six-membered ring diphosphinesJournal of the American Chemical Society, 1981
- Asymmetric synthesis. Production of optically active amino acids by catalytic hydrogenationJournal of the American Chemical Society, 1977
- Asymmetric hydrogenation. Rhodium chiral bisphosphine catalystJournal of the American Chemical Society, 1977
- Asymmetric hydrogenation with new chiral functionalized bisphosphine-rhodium complexesJournal of the American Chemical Society, 1976
- Asymmetric catalytic reduction with transition metal complexes. I. Catalytic system of rhodium(I) with (-)-2,3-0-isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane, a new chiral diphosphineJournal of the American Chemical Society, 1972
- Catalytic asymmetric hydrogenationJournal of the Chemical Society, Chemical Communications, 1972