Enantioselective synthesis of (R)-(−)-baclofen via Ru(II)–BINAP catalyzed asymmetric hydrogenation
- 7 March 2003
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 14 (5) , 581-586
- https://doi.org/10.1016/s0957-4166(03)00024-7
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Cobalt(II) Chloride-Catalyzed Chemoselective Sodium Borohydride Reduction of Azides in WaterSynthesis, 2000
- Enantioselective synthesis of (R)-(−)-baclofen using Fischer-type carbene anionsTetrahedron: Asymmetry, 2000
- An efficient synthesis of (R)-(−)-baclofenTetrahedron: Asymmetry, 1999
- Enantioselective Synthesis of (R)-(-)-BaclofenSynlett, 1993
- GABA-uptake inhibitors: construction of a general pharmacophore model and successful prediction of a new representativeJournal of Medicinal Chemistry, 1991
- Synthesis and biochemical evaluation of baclofen analogs locked in the baclofen solid-state conformationJournal of Medicinal Chemistry, 1991
- Resolution of 4-Phenyl-2-pyrrolidinone: A Versatile Synthetic IntermediateSynthesis, 1991
- (–)Baclofen decreases neurotransmitter release in the mammalian CNS by an action at a novel GABA receptorNature, 1980
- Synthesis of 4-cyano-4'-halobiphenylsThe Journal of Organic Chemistry, 1976
- The Preparation of Some β-Aryl-β-carboxypiperidonesJournal of the American Chemical Society, 1959