share
Chin. J. Org. Chem. ›› 2008, Vol. 28 ›› Issue (9): 1566-1571. Previous Articles Next Articles
Original Articles
金蔚蔚; 吴文彦; 张 倩*; 夏 鹏
收稿日期:
修回日期:
发布日期:
通讯作者:
JIN, Wei-Wei ; WU, Wen-Yan ; ZHANG, Qian* ; XIA, Peng
Received:
Revised:
Published:
Contact:
Share
Some different demethylation products and the double bond isomer of 2-bromo-4-[1-eth-(E)- ylidene-2-(4-methoxy-phenyl)-butyl]-1-methoxy-benzene (3) were obtained under different conditions dur-ing synthesizing 3’-methoxyl-1,2-diethystilbestrol (2). The angiogenesis inhibitory activities of some com-pounds were evaluated on human umbilical vein endothelial cells and the assay data indicated that the groups substituted on the skeleton of diethystilbestrol analogs could significantly affect their anti-angiogenesis activities.
Key words: 2-bromo-4-[1-eth-(E)-ylidene-2-(4-methoxy-phenyl)-butyl]-1-methoxy-benzene, isomerisation of double bond reaction, angiogenesis inhibitor, demethylation reaction
JIN, Wei-Wei ; WU, Wen-Yan ; ZHANG, Qian* ; XIA, Peng. Demethylation and Double-Bond Isomerisation of 2-Bromo-4-[1-eth- (E)-ylidene-2-(4-methoxy-phenyl)-butyl]-1-methoxy-benzene[J]. Chin. J. Org. Chem., 2008, 28(9): 1566-1571.
Export EndNote|Reference Manager|ProCite|BibTeX|RefWorks