Enantioselective borane reduction of ketones with oxazaborolidines boron-bound to nickel boride nanoparticles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Reduction of Carbonyl Compounds with Chiral Oxazaborolidine Catalysts: A New Paradigm for Enantioselective Catalysis and a Powerful New Synthetic Method
2. An asymmetric synthesis of MK-0417. Observations on oxazaborolidine-catalyzed reductions
3. Asymmetric synthesis using chirally modified borohydrides. Part 4. Enantio-selective reduction of ketones and oxime ethers with the reagent prepared from borane and polymer-supported (S)-(–)-2-amino-3-(p-hydroxyphenyl)-1,1-diphenylpropan-1-ol
4. Asymmetric synthesis using chirally modified borohydrides. Part 2. Enantioselective reduction of ketones with polymeric (S)-prolinol–borane reagent
5. Some enantioselective borane reductions of prochiral ketones catalysed by polymer-supported oxazaborolidines bound via the boron atom
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