Chiral monoaminoalcohols and diaminoalcohols of squaric acid: new catalysts for the asymmetric reduction of ketones by borane
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference21 articles.
1. Asymmetric boron-catalyzed reactions
2. Reduction of Carbonyl Compounds with Chiral Oxazaborolidine Catalysts: A New Paradigm for Enantioselective Catalysis and a Powerful New Synthetic Method
3. New chiral phosphinamide catalysts for highly enantioselective reduction of ketones
4. A Novel Phosphinamide Catalyst for the Asymmetric Reduction of Ketones by Borane
5. Chiral phosphinamides: new catalysts for the asymmetric reduction of ketones by borane
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1. Quaternary Phosphonium Salts as Active Brønsted Acid Catalysts for Friedel–Crafts Reactions;Organic Letters;2019-07-02
2. Applications of Chiral Squaramides: From Asymmetric Organocatalysis to Biologically Active Compounds;The Chemical Record;2016-03-10
3. Chiral polyethers derived from BINOL and ECH as highly enantioselective and efficient catalysts for the borane reduction of prochiral ketones;Journal of Molecular Catalysis A: Chemical;2015-03
4. Design and synthesis of novel C2-symmetric chiral shift reagents derived from squaramide and their recognition of anions and chiral carboxylate anions;Arkivoc;2014-09-13
5. A Polystyrene-Supported, Highly Recyclable Squaramide Organocatalyst for the Enantioselective Michael Addition of 1,3-Dicarbonyl Compounds to β-Nitrostyrenes;Advanced Synthesis & Catalysis;2012-10-05
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