65612-84-2Relevant articles and documents
Formal total synthesis of artocarpin
Mizota, Isao,Taniguchi, Kana,Shimizu, Makoto
, p. 310 - 322 (2017/03/14)
A formal total synthesis of artocarpin was achieved via selective demethylation, iodination, followed by Suzuki-Miyaura coupling reaction of the key flavone derivative. It took only 7 steps in the overall yield of 55% starting from commercially available 3,5-dimethoxyphenol.
Natural product analogues Albanin A/E and its preparation method and application
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, (2016/10/07)
The invention discloses a natural product Albanin A/E analogue. The inventor does research and prepares the natural product Albanin A/E analogue with the flavonoids compound framework structure on the basis of the natural product Albanin A and the natural product Albanin E, and complete synthesis and in-depth study of cervical cancer cell resistance activity are conducted on the natural product Albanin A/E analogue. The in-vitro cancer cell inhibition activity test shows that the compound has obvious effects on inhibiting cervical cancer Hela cells, and can be used for preparing candidate medicine for treating cervical cancer.