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Practical and Useful Methods for the Enantioselective Reduction of Unsymmetrical Ketones

Synthesis · 1992 · Vol. 1992(07) · pp. 605–617
Vinod K. Singh

Abstract

Enantioselective reduction of unsymmetrical ketones to optically active alcohols is very important in organic synthesis. Catalytic methods have been developed for this process and have not been reviewed previously. In this article the recently developed oxazaborolidine catalyzed reduction along with other useful reagents will be discussed. 1. Introduction 2. Oxazaborolidines 3. B-3-pinanyl-9-borabicyclo[3.3.1]nonane 4. Chlorodiisopinocampheylborane 5. 2,5-Dimethylborolane 6. BINAL-H 7. BINAP-Ru Complex 8. Conclusion

Asymmetric Hydrogenation and CatalysisAsymmetric Synthesis and CatalysisChemical Synthesis and ReactionsEnantioselective synthesisChemistryReagentReduction (mathematics)Optically activeCombinatorial chemistryCatalysisBINAPKetoneOrganic chemistry
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