Efficient Synthesis of 3-Methyl-Flavanones and Evaluation of Their Anti-Bacterial Activity
摘要:
AbstractA series of 2‐phenyl‐2,3‐dihydrochromon‐4‐one derivatives (flavanone derivatives) were synthesized by silica gel assisted isomerization of several α‐methyl‐2′‐hydroxy chalcones in 74%–88% yield. These flavanones were further oxidized to 3‐methyl flavones by using iodine in dimethyl sulphoxide at 60°C in presence of acid. The newly synthesized derivatives were evaluated for in vitro study against Staphylococcus aureus, Micrococcus luteus and Staphylococcus epidermis.
DOI:
10.1002/cjoc.201200254
作为产物:
描述:
在
adsorbed H2SO4 on silica gel 作用下,
以
二氯甲烷 为溶剂,
反应 3.0h,
以86%的产率得到2-(4-Methoxyphenyl)-3,6-dimethyl-2,3-dihydrochromen-4-one
参考文献:
名称:
Efficient Synthesis of 3-Methyl-Flavanones and Evaluation of Their Anti-Bacterial Activity
摘要:
AbstractA series of 2‐phenyl‐2,3‐dihydrochromon‐4‐one derivatives (flavanone derivatives) were synthesized by silica gel assisted isomerization of several α‐methyl‐2′‐hydroxy chalcones in 74%–88% yield. These flavanones were further oxidized to 3‐methyl flavones by using iodine in dimethyl sulphoxide at 60°C in presence of acid. The newly synthesized derivatives were evaluated for in vitro study against Staphylococcus aureus, Micrococcus luteus and Staphylococcus epidermis.