cis-1-amino-2-indanol in asymmetric synthesis. Part I. A practical catalyst system for the enantioselective borane reduction of aromatic ketones
- 1 September 1994
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 35 (36) , 6631-6634
- https://doi.org/10.1016/s0040-4039(00)73453-8
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Nitrogen Donors in Organometallic Chemistry and Homogeneous CatalysisAngewandte Chemie International Edition in English, 1994
- A practical process for the preparation of tetrahydro-1-methyl-3,3-diphenyl-1H,3H-pyrrolo[1,2-c][1,3,2]oxazaborole-borane. A highly enantioselective stoichiometric and catalytic reducing agentThe Journal of Organic Chemistry, 1993
- Asymmetric boron-catalyzed reactionsChemical Reviews, 1993
- In SituOxazaborolidines, Practical Enantioselective Hydride ReagentsSynlett, 1993
- Asymmetric syntheses with chiral oxazaborolidinesTetrahedron: Asymmetry, 1992
- A mechanistic and structural analysis of the basis for high enantioselectivity in the oxazaborolidine-catalyzed reduction of trihalomethyl ketones by catecholboraneTetrahedron Letters, 1992
- X-Ray crystal structure of a chiral oxazaborolidine catalyst for enantioselective carbonyl reductionTetrahedron Letters, 1992
- Synthesis and antiviral activity of a series of HIV-1 protease inhibitors with functionality tethered to the P1 or P1' phenyl designJournal of Medicinal Chemistry, 1992
- Practical and Useful Methods for the Enantioselective Reduction of Unsymmetrical KetonesSynthesis, 1992
- An efficient and catalytically enantioselective route to (S)-(-)-phenyloxiraneThe Journal of Organic Chemistry, 1988