Oxazaborolidine catalyzed enantioselective reductions of cyclic meso-imides
- 14 February 1994
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 35 (7) , 1087-1090
- https://doi.org/10.1016/s0040-4039(00)79972-2
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- 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
- Origins of the enantioselectivity observed in oxazaborolidine-catalyzed reductions of ketonesThe Journal of Organic Chemistry, 1993
- Highly Enantioselective Reduction of meso-Cyclic-1,2-dicarboximides. Asymmetric Synthesis of Bicyclic 2-Pyrrolidinone and Its 5-Hydroxy CongenerHETEROCYCLES, 1993
- Enantiomerically pure polyhydroxylated acyliminium ions. Synthesis of the glycosidase inhibitors (-)-swainsonine and (+)-castanospermineJournal of the American Chemical Society, 1990
- A facile synthesis of chiral bicyclic lactams utilized in the formation of chiral quaternary carbon compoundsThe Journal of Organic Chemistry, 1989
- Highly selective formation of cis-substituted hydroxylactams via auxiliary-controlled reduction of imidesThe Journal of Organic Chemistry, 1989
- Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implicationsJournal of the American Chemical Society, 1987
- AN ASYMMETRIC SYNTHESIS OF BICYCLIC LACTONES AND ITS APPLICATION TO THE ASYMMETRIC SYNTHESIS OF (1R,3S)-CIS-CHRYSANTHEMIC ACIDChemistry Letters, 1983
- Enzymes in organic synthesis. 24. Preparations of enantiomerically pure chiral lactones via stereospecific horse liver alcohol dehydrogenase catalyzed oxidations of monocyclic meso diolsJournal of the American Chemical Society, 1982