Quantum chemical modeling of chiral catalysis. Part 12. On the influence of the nature of the ring system on binding in ketone - borane complexes of chiral oxazaborolidines used as catalysts in the enantioselective reduction of ketones
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference23 articles.
1. Asymmetric syntheses with chiral oxazaborolidines
2. Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implications
3. New enantioselective routes to biologically interesting compounds
4. X-Ray crystal structure of a chiral oxazaborolidine catalyst for enantioselective carbonyl reduction
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3. Density functional study on enantioselective reduction of keto oxime ether with borane catalyzed by oxazaborolidine;Science in China Series B: Chemistry;2006-08
4. A Model for Double Asymmetric Induction in the Stereocontrolled Reduction of Glycosyl α-Ketoesters with Oxazaborolidines;Journal of the American Chemical Society;2004-05-14
5. Quantum chemical study on enantioselective reduction of keto oxime ether with borane catalyzed by oxazaborolidine. Part 5. The reduction process in which oxime is reduced first and carbonyl is reduced through a four-membered ring and a seven-membered ring intermediates;Journal of Molecular Structure: THEOCHEM;2004-01
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