Solvent effects on the diastereoselection in LiAlH4 reduction of α-substituted ketones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference30 articles.
1. Torsional strain involving partial bonds. The stereochemistry of the lithium aluminium hydride reduction of some simple open-chain ketones
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3. Reversal of .pi.-facial diastereoselection upon electronegative substitution of the substrate and the reagent
4. Stereoselectivities of nucleophilic additions to cyclohexanones substituted by polar groups. Experimental investigation of reductions of trans-decalones and theoretical studies of cyclohexanone reductions. The influence of remote electrostatic effects
5. On the Origin ofπ-Facial Diastereoselectivity in Addition Reactions of Cyclohexane-Based Systems
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