Synthesis of some new biflavonoids. I. Synthesis of the aromatic 1,4-diketones
Five arom. 1,4-diketones I [R = 2,4,6-(MeO)3, H, 4-Me, 4-MeO, 2,4-(MeO)2] were prepd. using succinyl chloride as acylating reagent. Arom. 1,4-diketone I [R = 2,4,6-(MeO)3] was also prepd. by using succinic anhydride as acylating reagent. The first method could be used for the prepn. of arom. 1,4-diketones with the same arom. groups, and the second for the different arom. groups. [on SciFinder (R)]
1989
25
3
60
3
CAN 114:5946
25-16
Benzene, Its Derivatives, and Condensed Benzenoid Compounds
Lanzhou Univ.,Lanzhou,Peop. Rep. China.
Journal
written in Chinese.
543-20-4 (Succinyl chloride) Role: RCT (Reactant), RACT (Reactant or reagent) (acylation by, of arom. compds.); 108-30-5 (Succinic anhydride) Role: RCT (Reactant), RACT (Reactant or reagent) (acylation by, of trimethoxybenzene); 71-43-2 (Benzene); 100-66-3 (Methoxybenzene); 108-88-3 (Toluene); 151-10-0; 621-23-8 Role: RCT (Reactant), RACT (Reactant or reagent) (acylation of, with succinyl chloride); 131002-94-3P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and acylation by, of trimethoxybenzene); 63213-25-2P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and chlorination of); 495-71-6P; 13145-56-7P; 15982-64-6P; 16290-20-3P; 120341-51-7P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of)
REVIEWED
OTHER