A theoretical investigation of the enantioselective reduction of prochiral ketones promoted by chiral diamines
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference33 articles.
1. Reduction of Carbonyl Compounds with Chiral Oxazaborolidine Catalysts: A New Paradigm for Enantioselective Catalysis and a Powerful New Synthetic Method
2. Enantiomerically Pure Compounds via Chiral Organoboranes
3. Asymmetric reduction with chiral organoboranes based on .alpha.-pinene
4. Asymmetric syntheses with chiral oxazaborolidines
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1. Insights into the origin of selectivity for [2+2] cycloaddition step reaction involved in the mechanism of enantioselective reduction of ketones with borane catalyzed by a B-methoxy oxazaborolidine catalyst derived from (–)-β-pinene: an HMDFT and combined topological ELF, NCI and QTAIM study;Theoretical Chemistry Accounts;2021-10-14
2. Recent Advances on Computational Investigations ofN-Heterocyclic Carbene Catalyzed Cycloaddition/Annulation Reactions: Mechanism and Origin of Selectivities;ChemCatChem;2017-12-11
3. Theoretical Investigations toward the Asymmetric Insertion Reaction of Diazoester with Aldehyde Catalyzed by N-Protonated Chiral Oxazaborolidine: Mechanisms and Stereoselectivity;The Journal of Physical Chemistry A;2015-07-16
4. Enantioselective Reaction;Organic Stereochemistry;2015-06-26
5. DFT study on the reaction mechanisms and stereoselectivities of NHC-catalyzed [2 + 2] cycloaddition between arylalkylketenes and electron-deficient benzaldehydes;Organic & Biomolecular Chemistry;2014-05-14
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