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)]


Published in:
Chinese Science Bulletin, 35, 9, 744-6
Year:
1990
Keywords:
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)
Laboratories:




 Record created 2010-11-25, last modified 2018-03-17


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