A theoretical investigation of cyclohexanone reduction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference12 articles.
1. The Stereochemistry of Hydride Reductions
2. On the Stereochemistry of the Reduction of Cyclic Ketones with Lithium Tri-t-butoxyaluminum Hydride
3. Torsional strain involving partial bonds. The steric course of the reaction between allyl magnesium bromide and 4-t-butyl-cyclohexanone
4. The influence of steric and torsional strain on the steric course of additions to cyclohexanones. The reaction between 4-T-butylcyclohexanone and T-butylallyl magnesium bromide.
5. Stereoselective organometallic alkylation reactions. II. Organomagnesium and organoaluminum addition to ketones having varied steric requirements. New concept of stereochemical control
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1. DFT and MP2 study on the electrophilic addition reaction of bromine to exo-tricyclo[3.2.1.02.4]oct-6-ene;Journal of Molecular Modeling;2009-11-11
2. Ab initio and DFT study on the electrophilic addition of bromine to endo-tricyclo[3.2.1.02,4]oct-6-ene;Journal of Molecular Modeling;2005-10-26
3. Diastereoselectivity in Gas-Phase Hydride Reduction Reactions of Ketones;Journal of the American Chemical Society;1999-07-21
4. Electronic Control of Facial Selection in Additions to Sterically Unbiased Ketones and Olefins;Chemical Reviews;1999-04-07
5. Theoretical studies on long-range substituent effects in the reduction of 7-norbornanones;J. Chem. Soc., Perkin Trans. 2;1996
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