Asymmetric oxazaborolidine-catalyzed reduction of prochiral ketones with N-tert-butyl-N-trimethylsilylamine–borane
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference21 articles.
1. Asymmetric syntheses with chiral oxazaborolidines
2. Reduction of Carbonyl Compounds with Chiral Oxazaborolidine Catalysts: A New Paradigm for Enantioselective Catalysis and a Powerful New Synthetic Method
3. Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implications
4. A stable and easily prepared catalyst for the enantioselective reduction of ketones. Applications to multistep syntheses
5. Role of NaBH4 Stabilizer in the Oxazaborolidine-Catalyzed Asymmetric Reduction of Ketones with BH3-THF
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2. Asymmetric reduction of ketones catalyzed by α,α-diphenyl-(L)-prolinol modified with imidazolium ionic liquid and BH3·SMe2 as a recoverable catalyst;Journal of Molecular Catalysis A: Chemical;2015-03
3. β-Hydroxyamide derivatives of salicylic acid as organocatalysts for enantioselective reductions of prochiral ketones;Tetrahedron: Asymmetry;2013-07
4. Borane - Amines;Fieser and Fieser's Reagents for Organic Synthesis;2013-04-26
5. Corey–Itsuno Reduction of Ketones: A Development of Safe and Inexpensive Process for Synthesis of Some API Intermediates;Organic Process Research & Development;2012-04-11
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