775315-33-8Relevant academic research and scientific papers
One-pot synthesis of 3-methylflavones and their transformation into (E)-3-styrylflavones via Wittig reactions
Rocha, Djenisa H. A.,Pinto, Diana C. G. A.,Silva, Artur M. S.
, p. 2683 - 2686 (2014/01/06)
An efficient one-pot synthesis of 3-methylflavone derivatives is established. Furthermore, their transformation into phosphorus ylides, which are then used in the diastereoselective synthesis of (E)-styrylflavones through Wittig reactions, is also studied
Synthesis of 3-methylflavones and their antioxidant and antibacterial activities
Jayashree, B. S.,Alam, Afroze,Vijay Kumar, D.,Nayak, Yogendra
, p. 1991 - 1996,6 (2020/07/30)
An attempt was made to synthesise newer 3-methylflavones with various substitution on the ring A and B of 2-phenylchromen-4-one. They were evaluated for antioxidant activity and antibacterial activity against the Gram-positive and Gram-negative bacteria.
Antioxidant and antibacterial activity of new 3-methylflavones
Jayashree,Alam, Afroze,Kumar, D. Vijay,Nayak, Yogendra
, p. 237 - 240 (2011/12/15)
Synthesis of new 3-methylflavones with various substitution on the ring A and B is being described. They were evaluated for antioxidant and antibacterial activity against Gram positive and Gram negative bacteria. Test compounds such as F-4,9,11,12 and 20
Lead optimization providing a series of flavone derivatives as potent nonsteroidal inhibitors of the cytochrome P450 aromatase enzyme
Gobbi, Silvia,Cavalli, Andrea,Rampa, Angela,Belluti, Federica,Piazzi, Lorna,Paluszcak, Anja,Hartmann, Rolf W.,Recanatini, Maurizio,Bisi, Alessandra
, p. 4777 - 4780 (2007/10/03)
Following our SAR studies on aromatase inhibitors, new compounds were designed by appropriately modifying the structure of flavone 1 using our previously reported CoMFA model. While the introduction of substituents on the 2-phenyl ring alone did not cause
