What Einstein Didn't Know (Wolke, Robert L.) von Stocker, Jack H

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Quantitative studies in stereochemistry. 16. The ratio of diastereomeric pinacols produced in the aluminum amalgam bimolecular reduction of acetophenone von Stocker, Jack H, Walsh, Donald J

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A Unique Reversal of Stereospecificity in the Addition of Phenyllithium vs. Phenylmagnesium Bromide to 1,2-Dicyclohexylethanedione-C14 von Stocker, Jack H

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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 Eff... von Stocker, Jack H

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Quantitative studies in stereochemistry. Electrochemistry. III. Ratio of diastereomeric pinacols produced in the electrolytic bimolecular reduction of 2-acetylpyridine. Formation o... von Stocker, Jack H, Jenevein, Roy M

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Quantitative studies in stereochemistry. Electrochemistry. II. The ratio of diastereomeric glycols formed in the electrolytic bimolecular reduction of benzaldehyde and propiophenon... von Stocker, Jack H, Jenevein, Roy M

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Quantitative studies in stereochemistry. B. Photochemistry. III. Ratios of diastereomeric pinacols formed in the ultraviolet-promoted bimolecular reduction of selected para-substit... von Stocker, Jack H, Kern, David H, Jenevein, Roy M

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Quantitative studies in stereochemistry. Series B. Photochemistry. V. Ratio of diastereomeric pinacols formed in the ultraviolet-promoted biomolecular reduction of deoxybenzoin von Stocker, Jack H, Kern, David H

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Quantitative studies in stereochemistry. XV. Photochemistry. VIII. Photochemical interconversion of diastereomeric acetophenone pinacols induced by shorter wavelength ultraviolet i... von Stocker, Jack H, Kern, David H

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Quantitative studies in stereochemistry. B. Photochemistry. II. Solvent and basicity effects on the ratio of diastereomeric glycols formed in the ultraviolet-promoted bimolecular r... von Stocker, Jack H, Kern, David H

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Quantitative Studies in Stereochemistry by Isotope Dilution. Series B. Photochemistry. The Ratio of Diastereoisomeric Glycols Formed in the Ultraviolet-Promoted Bimolecular Reducti... von Stocker, Jack H, Kern, David H

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Quantitative studies in stereochemistry by isotope dilution. C. Electrochemistry. I. Ratio of diastereomeric pinacols formed in the electrolytic bimolecular reduction of acetopheno... von Stocker, Jack H, Jenevein, Roy M

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The Effect of Changing Reagent upon Stereoselectivity1a von Stocker, Jack H, Sidisunthorn, Padet, Benjamin, Ben M, Collins, Clair J

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Quantitative studies in stereochemistry. XIII. Peroxide-induced pinacolization of acetophenone. Thermal stability of the acetophenone pinacols von Stocker, Jack H, Kern, David H

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Quantitative studies in stereochemistry. Series B. Photochemistry. IV. Ratios of diastereomeric pinacols formed in the ultraviolet-promoted bimolecular reduction of acetophenone-7-... von Stocker, Jack H, Kern, David H

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Quantitative studies in stereochemistry. Photochemistry. VII. Electrochemistry. 4. Photochemical and electrochemical bimolecular reduction of aldehydes and unsymmetrical ketones. C... von Stocker, Jack H, Jenevein, Roy M, Kern, David H

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The electrochemical transformation of ααα-trifluoroacetophenone into acetophenone; an unusually ready hydrogenolysis of the C–F bond von Stocker, Jack H., Jenevein, Roy M.

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Electrochemistry of Biological Molecules von Dryhurst, G., Stocker, Jack H.

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A Unique Reversal of Stereospecificity in the Addition of Phenyllithium vs. Phenylmagnesium Bromide to 1,2-Dicyclohexylethanedione-C 14 von Stocker, Jack H.

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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 Eff... von Stocker, Jack H.

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