| Title | Asymmetric Hydrogenation of alpha-Primary and Secondary Amino Ketones: Efficient Asymmetric Syntheses of (-)-Arbutamine and (-)-Denopamine. | | Author(s) | Shang G, Liu D, Allen SE, Yang Q, Zhang X | | Institution | Department of Chemistry, The Pennsylvania State University, 104 Chemistry Building, University Park, PA 16802, USA. | | Source | Chemistry 2007 Jun 25. | | Abstract | Two beta-receptor agonists (-)-denopamine and (-)-arbutamine were prepared in good yields and enantioselectivities by asymmetric hydrogenation of unprotected amino ketones for the first time by using Rh catalysts bearing electron-donating phosphine ligands. A series of alpha-primary and secondary amino ketones were synthesized and hydrogenated to produce various 1,2-amino alcohols in good yields and with good enantioselectivies. This Rh electron-donating phosphine-catalyzed asymmetric hyderogenation represents one of the most promising and convenient approaches towards the asymmetric synthesis of chiral amino alcohols. | | Language | ENG | | Pub Type(s) | JOURNAL ARTICLE
| | PubMed ID | 17591728 |
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