Experimental transition state for the B-chlorodiisopinocampheylborane (DIP-Cl) reduction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference30 articles.
1. Chiral synthesis via organoboranes. 14. Selective reductions. 41. Diisopinocampheylchloroborane, an exceptionally efficient chiral reducing agent
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3. Thermal reactions of B-alkyl-9-borabicyclo[3.3.1]nonane (9-BBN). Evidence for unusually facile dehydroboration with B-pinanyl-9-BBN
4. Relationship between the structure and enantioselectivity in the asymmetric reduction of 2′,6′-disubstituted acetophenones with DIP-ChlorideTM. An ab initio study
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1. The Corey-Bakshi-Shibata Reduction: Mechanistic and Synthetic Considerations - Bifunctional Lewis Base Catalysis with Dual Activation;Lewis Base Catalysis in Organic Synthesis;2016-08-17
2. (+)-B-Chlorodiisopinocampheylborane;Encyclopedia of Reagents for Organic Synthesis;2015-04-01
3. New Applications of Isotope Effects in the Determination of Organic Reaction Mechanisms;Advances in Physical Organic Chemistry;2012
4. Oxidation and Reduction;Organic Reaction Mechanisms Series;2011-12-06
5. Reactions of Aldehydes and Ketones and their Derivatives;Organic Reaction Mechanisms Series;2011-12-06
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