Steroidal silicon side-chain analogs as potential antifertility agents
摘要:
A number of silicon-substituted analogues of ethynylestradiol that exhibit modified and enhanced biological activities have been synthesized. Particularly noteworthy are a group of [(trialkylsilyl)ethynyl]estradiol analogues that exhibit high antifertility potency and markedly reduced estrogenic activity. The best compounds synthesized are 17 alpha-[(triethylsilyl)ethynyl]estradiol (5) and 17 alpha-[(tert-butyldimethylsilyl)ethynyl]estradiol (33), which show a separation of antifertility from estrogenic activity in the rat. The results of structure-activity studies indicate a good correlation between the observed biological activities and the calculated van der Waals volumes of the three variable silicon substituents.
Transformations of (chloromethyl)silacycloalkanes under the influence of aluminum chloride
作者:N. S. Nametkin、V. M. Vdovin、K. S. Pushchevaya、A. N. Egorochkin
DOI:10.1007/bf00911854
日期:1967.11
Steroidal silicon side-chain analogs as potential antifertility agents
作者:Richard H. Peters、David F. Crowe、Masato Tanabe、Mitchell A. Avery、Wesley K. M. Chong
DOI:10.1021/jm00387a011
日期:1987.4
A number of silicon-substituted analogues of ethynylestradiol that exhibit modified and enhanced biological activities have been synthesized. Particularly noteworthy are a group of [(trialkylsilyl)ethynyl]estradiol analogues that exhibit high antifertility potency and markedly reduced estrogenic activity. The best compounds synthesized are 17 alpha-[(triethylsilyl)ethynyl]estradiol (5) and 17 alpha-[(tert-butyldimethylsilyl)ethynyl]estradiol (33), which show a separation of antifertility from estrogenic activity in the rat. The results of structure-activity studies indicate a good correlation between the observed biological activities and the calculated van der Waals volumes of the three variable silicon substituents.
Chemistry of organosilicon compounds
作者:Hideki Sakurai、Toshifumi Hirose、Akira Hosomi
DOI:10.1016/s0022-328x(00)89612-6
日期:1975.2
The intramolecular hydrosilylation of (4-pentenyl)hydrosilanes with transitionmetal salt catalysts afforded five- and six-membered ring-closure products in high yields, with the former predominating. This has been rationalized in terms of a reaction scheme based on the Harrod—Chalk mechanism in which both Si-metal and C-metal bonds were involved. The seven-membered intermediate leading to the six-membered