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Asymmetric Hydrogenation of Unsaturated Ureas with the BIPI Ligands.
- Source :
-
Organic Letters . Jan2008, Vol. 10 Issue 2, p341-344. 4p. - Publication Year :
- 2008
-
Abstract
- Asymmetric hydrogenation of unsaturated urea esters with the BIPI Ligands has been examined. Optimization of the P−N ligand structure has led to the development of chiral rhodium catalysts capable of producing the targets with >99% ee. The critical phosphine borane SNAr reaction needed for ligand synthesis has been optimized to give the adducts in high yield at ambient temperature with no racemization. An extremely concise, economical, and scalable sequence to these important new ligands for catalysis of asymmetric hydrogenation has been developed. [ABSTRACT FROM AUTHOR]
- Subjects :
- *NITROGEN excretion
*URINE
*PHOSPHORUS compounds
*SURFACE chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 15237060
- Volume :
- 10
- Issue :
- 2
- Database :
- Academic Search Index
- Journal :
- Organic Letters
- Publication Type :
- Academic Journal
- Accession number :
- 28693655
- Full Text :
- https://doi.org/10.1021/ol7028542