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Quantitative Studies in Stereoselective Addition Reactions by Isotope Dilution. Additions of Organometallic Reagents Leading to 2,3-Dicyclohexyl-2,3-butanediol. A Strong Halide Effect1
National licenceAmerican Chemical Society | 1964| -
A Unique Reversal of Stereospecificity in the Addition of Phenyllithium vs. Phenylmagnesium Bromide to 1,2-Dicyclohexylethanedione-C14
National licenceAmerican Chemical Society | 1966| -
Quantitative studies in stereochemistry by isotope dilution. C. Electrochemistry. I. Ratio of diastereomeric pinacols formed in the electrolytic bimolecular reduction of acetophenone-7-14C
National licenceAmerican Chemical Society | 1968| -
Quantitative studies in stereochemistry. Electrochemistry. II. The ratio of diastereomeric glycols formed in the electrolytic bimolecular reduction of benzaldehyde and propiophenone
National licenceAmerican Chemical Society | 1968| -
Quantitative Studies in Stereochemistry by Isotope Dilution. Series B. Photochemistry. The Ratio of Diastereoisomeric Glycols Formed in the Ultraviolet-Promoted Bimolecular Reduction of Acetophenone-7-C14
National licenceAmerican Chemical Society | 1966| -
Quantitative studies in stereochemistry. 16. The ratio of diastereomeric pinacols produced in the aluminum amalgam bimolecular reduction of acetophenone
National licenceAmerican Chemical Society | 1979| -
Quantitative studies in stereochemistry. Series B. Photochemistry. IV. Ratios of diastereomeric pinacols formed in the ultraviolet-promoted bimolecular reduction of acetophenone-7-14C in amine media
National licenceAmerican Chemical Society | 1968| -
Quantitative studies in stereochemistry. Series B. Photochemistry. V. Ratio of diastereomeric pinacols formed in the ultraviolet-promoted biomolecular reduction of deoxybenzoin
National licenceAmerican Chemical Society | 1968| -
Quantitative studies in stereochemistry. XV. Photochemistry. VIII. Photochemical interconversion of diastereomeric acetophenone pinacols induced by shorter wavelength ultraviolet irradiation
National licenceAmerican Chemical Society | 1971| -
Quantitative studies in stereochemistry. XIII. Peroxide-induced pinacolization of acetophenone. Thermal stability of the acetophenone pinacols
National licenceAmerican Chemical Society | 1970| -
The photochemical transformation of phenyl cyclohexyl ketone into acetophenone; an unusual double type-II cleavage
National licenceRoyal Society of Chemistry | 1969| -
The electrochemical transformation of ααα-trifluoroacetophenone into acetophenone; an unusually ready hydrogenolysis of the C–F bond
National licenceRoyal Society of Chemistry | 1968| -
Quantitative studies in stereochemistry. Photochemistry. VII. Electrochemistry. 4. Photochemical and electrochemical bimolecular reduction of aldehydes and unsymmetrical ketones. Common stereochemistry
National licenceAmerican Chemical Society | 1969| -
Quantitative studies in stereochemistry. B. Photochemistry. III. Ratios of diastereomeric pinacols formed in the ultraviolet-promoted bimolecular reduction of selected para-substituted acetophenones
National licenceAmerican Chemical Society | 1968| -
The Effect of Changing Reagent upon Stereoselectivity1a
National licenceAmerican Chemical Society | 1960|
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