1379473-99-0Relevant articles and documents
Synthetic transformations of sesquiterpene lactones. IV.* synthesis and transformations of gem-dichlorocyclopropyl-substituted isoalantolactone derivatives
Shul'ts,Belovodskii,Shakirov,Gatilov,Pokrovskii,Pokrovskii,Tolstikov
, p. 238 - 244 (2012/09/07)
Chloro-containing compounds, the ratio of which depended on the reaction time, were formed via reaction of isoalantolactone and CHCl3 through the action of a phase-transfer catalyst. 4,15-(2,2-Dichlorocycloprop-1-yl) isoalantolactone exhibited high activity and selectivity in the Heck reaction with arylhalides. Data for the cytotoxicity of the synthesized chloro-derivatives of isoalantolactone in CEM-13, MT-4, and U-937 cell tumor models were obtained. The doses of the most active compounds inhibiting the viability of tumor cells by 50% (CCID50) were 3.2-11.1 μM.