74693-73-5Relevant academic research and scientific papers
Isoflavans derivatives as inhibitors of soybean lipoxygenase: In-vitro and docking studies
Mascayano, Carolina,Rezende, Marcos Caroli,Rivera, Yenifer,Espinosa, Victoria
body text, p. 935 - 937 (2012/05/05)
The lipoxygenases (LOX) are a family of non-heme iron-containing dioxygenases which catalyze the stereospecific insertion of molecular oxygen into arachidonic acid, leading to hydroxy derivatives as end products. In this work, we studied the behavior of s
Synthesis of a New Isoflavone Occuring in Tephrosia maxima (Pers)
Parmar, V. S.,Singh, Suddham,Jain, Rajni
, p. 484 - 485 (2007/10/02)
7,8-Methylenedioxy-3',4'-dimethoxyisoflavone (I), a new isoflavone isolated from the aerial parts and roots of Tephrosia maxima has been synthesized by oxidative rearrangement of 2'-hydroxy-3',4'-methylenedioxy-3,4-dimethoxychalcone (IV) with thallium(III) nitrate (TTN) in trimethyl orthoformate (TMOF), followed by acid-catalysed cyclization.It has also been synthesized from 2,3,4-trihydroxy-3',4'-dimethoxydeoxybenzoin (V).
A Convenient Synthesis of 6,7-Methylenedioxy-3',4'-dimethoxyisoflavone
Bhardwaj, D. K.,Bisht, M. S.,Jain, R. K.,Mehta, C. K.
, p. 82 - 84 (2007/10/02)
6,7-Methylenedioxy-3',4'-dimethoxyisoflavone (I) has been synthesized from 2',4',5'-tribenzyloxy-3,4-dimethoxy-chalkone (III).The epoxide (IV) of III is converted into the isoflavone (VI) trough the α-formyldesoxybenzoin (V).Methylenation of VI gives I.
