作者:Isidro S. Marcos、Rosalina F. Moro、Isabel Costales、Pilar Basabe、David Díez、Faustino Mollinedo、Julio G. Urones
DOI:10.1016/j.tet.2012.07.010
日期:2012.9
The synthesis of 12-epi-ent-polyalthenol, 10, and its epimer at C-19, 11, from ent-halimic acid as starting material has been carried out. The structure of the natural product polyalthenol 1 is confirmed in this way. The synthesized indole sesquiterpenes 10 and 11 and their acetylderivatives 32 and 33 inhibited cellular proliferation of a number of human leukaemic and solid tumour cell lines.
12-合成外延- ENT -polyalthenol,10,其在C-19,差向异构体11,从ENT -halimic羧酸作为起始物质已被进行。以此方式确认了天然产物聚苯酚1的结构。合成的吲哚倍半萜10和11及其乙酰基衍生物32和33抑制了许多人白血病和实体瘤细胞系的细胞增殖。