1384552-67-3Relevant academic research and scientific papers
Synthesis of novel benzosuberone derivatives using organophosphorus reagents and their antitumor activities
Boulos, Leila S.,Abdel-Malek, Hoda A.,El-Sayed, Naglaa F.
experimental part, p. 243 - 252 (2012/06/30)
2-Arylidenebenzosuberones react with a Wittig-Horner reagent in the presence of sodium hydride as a base to give the novel dimethyl (4-(4-methoxyphenyl)-2-oxa-2,3,4,5,6,7-hexahydrobenzo-[6,7]cyclohepta[1,2-b] pyran-3-yl)phosphonate. On the other hand, 6,7-dihydrobenzo[6,7]cyclohepta-[1,2- b]pyran-2(5H)-ones were isolated from the reaction of 2-arylidenebenzosuberones with Wittig-Horner reagents using alcoholic sodium alkoxide. The reaction of 2-arylidenebenzosuberones with trialkyl phosphites affords the alkyl phosphonate derivatives. Tris(dialkylamino)phosphines react with 2-arylidenebenzosuberones to give the oxaphospholanoxide products. 2-Arylidenebenzosuberones react with Lawesson's reagent to yield the corresponding dimers. Some of the prepared products were screened for antitumor activity.
