Infoscience

Journal article

Study on the synthesis of some new biflavonoids. (VI). The catalytic hydrogenation of 3,3"-biflavones

The biflavone I was hydrogenated and the configuration of the chamaejasmin-type biflavone products was detd. [on SciFinder (R)]

    Keywords: Configuration (abs. ; of trimethoxydiphenylbibenzopyrandione) ; methoxydiphenylbibenzopyran hydrogenation; bibenzopyran methoxydiphenyl hydrogenation; chamaejasmin analog prepn configuration

    Note:

    CAN 114:6071

    26-4

    Biomolecules and Their Synthetic Analogs

    Lab. Appl. Org. Chem.,Lanzhou Univ.,Lanzhou,Peop. Rep. China.

    Journal

    1001-6538

    written in English.

    131036-43-6P; 131036-44-7P Role: FORM (Formation, nonpreparative), PREP (Preparation) (formation of, in hydrogenation of trimethoxydiphenylbibenzopyrandione); 120341-56-2 Role: RCT (Reactant), RACT (Reactant or reagent) (hydrogenation of); 69618-96-8DP (Chamaejasmin) Role: PRP (Properties), SPN (Synthetic preparation), PREP (Preparation) (prepn. and abs. configuration of); 131036-42-5P Role: PRP (Properties), SPN (Synthetic preparation), PREP (Preparation) (prepn. and configuration of); 131036-41-4P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. and hydrogenation and configuration of)

    Reference

    • EPFL-ARTICLE-158218

    Record created on 2010-11-25, modified on 2016-08-08

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