Reversible dimerisation of ephedrine-derived oxazaborolidines
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference23 articles.
1. Asymmetric syntheses with chiral oxazaborolidines
2. Catalytic Behavior of Optically Active Amino Alcohol–Borane Complex in the Enantioselective Reduction of Acetophenone OximeO-Alkyl Ethers
3. Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implications
4. Synthesis of allylic alcohols via palladium-catalyzed cross-coupling of vinylic epoxides and aryl or vinylic halides and triflates
5. First application of attractive intramolecular interactions to the design of chiral catalysts for highly enantioselective Diels-Alder reactions
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1. Chiral Aminoalcohols and Squaric Acid Amides as Ligands for Asymmetric Borane Reduction of Ketones: Insight to In Situ Formed Catalytic System by DOSY and Multinuclear NMR Experiments;Molecules;2021-11-14
2. Tetrahydro-1-methyl-3,3-diphenyl-1H, 3H-pyrrolo[1,2-c][1,3,2]oxazaborole;Encyclopedia of Reagents for Organic Synthesis;2013-09-16
3. A DFT study of the enantioselective reduction of oxime ethers promoted by chiral spiroborate esters;International Journal of Quantum Chemistry;2011-05-16
4. Chiral Epoxides via Borane Reduction of 2-Haloketones Catalyzed by Spiroborate Ester: Application to the Synthesis of Optically Pure 1,2-Hydroxy Ethers and 1,2-Azido Alcohols;The Journal of Organic Chemistry;2011-02-04
5. Spiroborate Ester-Mediated Asymmetric Synthesis of β-Hydroxy Ethers and Its Conversion to Highly Enantiopure β-Amino Ethers;The Journal of Organic Chemistry;2009-05-04
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