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Asymmetric hydrogenation of unsaturated ureas with the BIPI ligands
- Source :
- Organic letters. 10(2)
- Publication Year :
- 2007
-
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.
- Subjects :
- Molecular Structure
Ligand
Phosphines
Organic Chemistry
Asymmetric hydrogenation
chemistry.chemical_element
Esters
Stereoisomerism
Borane
Ligands
Biochemistry
Catalysis
Rhodium
chemistry.chemical_compound
chemistry
Nucleophilic aromatic substitution
Organic chemistry
Urea
Hydrogenation
Physical and Theoretical Chemistry
Racemization
Phosphine
Subjects
Details
- ISSN :
- 15237060
- Volume :
- 10
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- Organic letters
- Accession number :
- edsair.doi.dedup.....c3fc8d4ad3b24e0a109f92e2690ebd08