90486-63-8Relevant articles and documents
Synthesis of Pyranoisoflavones from Pyronochalcones: Synthesis of Elongatin and Its Angular Isomer
Tsukayama, Masao,Kawamura, Yasuhiko,Tamaki, Hiroto,Kubo, Tomoya,Horie, Tokunaru
, p. 826 - 832 (2007/10/02)
Elongatin (4',5-dihydroxy-2',5'-dimethoxy-2'',2''-dimethylpyranoisoflavone) was synthesized by an oxidative rearrangement of the corresponding pyronochalcone with thallium(III) nitrate and a regioselective reduction of 7-(4-benzoyloxy-2,5-dimethoxyphenyl)-2,3-dihydro-2,2-dimethyl-5-tosyloxy-4H,6H-benzodipyran-4,6-dione with sodium borohydride-palladium chloride, followed by dehydration of the resultant alcohol and hydrolysis.Its angular isomer (4',5-dihydroxy-2',5'-dimethoxy-2'',2''-dimethylpyranoisoflavone) was also synthesized from the corresponding pyronochalcone in a similar manner.
A CONVENIENT SYNTHESIS OF A LINEAR PYRANOISOFLAVONE: SYNTHESIS OF ELONGATIN AND ITS ANGULAR ISOMER
Tsukayama, Masao,Iguchi, Yukihisa,Horie, Tokunaru,Masumura, Mitsuo,Nakayama, Mitsuru
, p. 709 - 712 (2007/10/02)
Linear 4',5-dihydroxy-2',5'-dimethoxy-2",2"-dimethyl-dihydropyranoisoflavone, which had been prepared from 6-acetyl-5-benzyloxy-7-hydroxy-2,2-dimethylchroman via four steps, was dehydrogenated with DDQ to give elongatin.Its angular isomer was als