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                <identifier>oai:data.mendeley.com/x97s9ypxjz.1</identifier>
                <datestamp>2023-08-13T06:42:30Z</datestamp>
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    <dc:creator>Krstenansky, John</dc:creator>
    <dc:title>NMR spectra of substituted alpha-aminonitrilecyclohexane mixtures.</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>The NMR spectra of product mixtures resulting from the reaction of substituted cyclohexanones with an amine hydrochloride and potassium cyanide in water.  The resulting products exhibit a preference for one of the two possible geometric isomers due to diastereofacial selectivity during the attack by the cyanide ion on the intermediate iminium. A pdf file is included as a key to the identity of the folders containing the NMR data on the individual compounds.</dc:description>
    <dc:subject>Stereochemistry</dc:subject>
    <dc:subject>Nuclear Magnetic Resonance Spectroscopy</dc:subject>
    <dc:subject>Selectivity</dc:subject>
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    <dc:date>2023-08-13T06:42:30Z</dc:date>
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