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Claisen-type addition of glycine to a pyridoxal iminium ion in water.

Claisen-type addition of glycine to a pyridoxal iminium ion in water. Research Abstract Details 

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  • Claisen-type addition of glycine to a pyridoxal iminium ion in water. Abstract Text:

    krisztina tothKrisztina Toth,lauren m gaskellLauren M Gaskell,john p richardJohn P Richard,

    The 5'-deoxypyridoxal stabilized glycine carbanion has been generated in water at neutral and mildly basic pH. At pH < 7, this carbanion reacts mainly with the carbonyl carbon of 1 to form a stable Claisen-type adduct. At pH > or = 8, this carbanion reacts with the iminium carbon of the pyridoxal-glycine iminium ion to form the second Claisen-type adduct 3 as the major reaction product.

    Claisen-type addition of glycine to a pyridoxal iminium ion in water. Publishing Authors By Initials

    k tothK Toth,lm gaskellLM Gaskell,jp richardJP Richard,

    For similar abstracts research abstracts see: abstracts research

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    Claisen-type addition of glycine to a pyridoxal iminium ion in water. Journal Published:

    PUBLICATION TYPE: Research Support, U.S. Gov't,

    Journal: The Journal of organic chemistry

    VOLUME: 71

    Page Numbers: 7094-6

    Journal Abbreviation:

    ISSN: 0022-3263

    DAY: 1

    MONTH: Sep

    YEAR: 2006

    Claisen-type addition of glycine to a pyridoxal iminium ion in water. Information

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    LANGUAGE: eng

    NlmUniqueID: 2985193

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    Grant and Affiliation Information for Claisen-type addition of glycine to a pyridoxal iminium ion in water.

    AFFILIATION: Department of Chemistry, University of Buffalo, State University of New York, Buffalo, NY 14260-3000, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: J Org Chem

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