Asymmetric Reduction of Acetophenone with Borane Catalyzed by Chiral Oxazaborolidinones Derived from L-α-Amino Acids
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397910008086884
Reference16 articles.
1. Preparation of optically active benzyl-.alpha.-d alcohol via reduction by B-3.alpha.-pinanyl-9-borabicyclo[3.3.1]nonane. A new highly effective chiral reducing agent
2. ASYMMETRIC REDUCTION OF a,b-ACETYLENIC KETONES WITH B-3-PINANYL-9-BORABICYCLO[3.3.1]NONANE: (R)-( + )-1-OCTYN-3-OL
3. Asymmetric reduction of ketones with B-(cis-10-pinanyl)-9-borabicyclo[3.3.1]nonane. Observation of a change in enantioselection between similar organoborane and organoaluminum reagents
4. Selective reductions. 37. Asymmetric reduction of prochiral ketones with B-(3-pinanyl)-9-borabicyclo[3.3.1]nonane
5. Chiral synthesis via organoboranes. 14. Selective reductions. 41. Diisopinocampheylchloroborane, an exceptionally efficient chiral reducing agent
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3. Synthesis of N-squaramidoacids and their application in asymmetric borane reduction of prochiral ketones;Chinese Journal of Chemistry;2010-08-26
4. A Genetically Encoded Boronate-Containing Amino Acid;Angewandte Chemie International Edition;2008-10-13
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