-transparent.png){kind=logo}
Various 17 alpha-ethynylsteroids were prepared and derivatized as the corresponding triethylsilyl compounds 2-35, which were examined for a ratio of antifertility to estrogenic activity that would be more beneficial than that of the presently used agent. Among the triethylsilyl compounds evaluated, only 23 displayed this desired ratio, although two other compounds without the triethylsilyl moiety, 18 and 26, shared similar characteristics.
Related Publications
R H Peters, and
D F Crowe, and
M A Avery, and
W K Chong, and
M Tanabe
January 1997,
Journal of andrology,
R H Peters, and
D F Crowe, and
M A Avery, and
W K Chong, and
M Tanabe
September 1983,
Journal of pharmaceutical sciences,
R H Peters, and
D F Crowe, and
M A Avery, and
W K Chong, and
M Tanabe
January 2012,
Pharmacological reports : PR,
R H Peters, and
D F Crowe, and
M A Avery, and
W K Chong, and
M Tanabe
September 1988,
Pharmaceutical research,
R H Peters, and
D F Crowe, and
M A Avery, and
W K Chong, and
M Tanabe
January 2017,
Mini reviews in medicinal chemistry,
R H Peters, and
D F Crowe, and
M A Avery, and
W K Chong, and
M Tanabe
March 2003,
Chemical & pharmaceutical bulletin,
R H Peters, and
D F Crowe, and
M A Avery, and
W K Chong, and
M Tanabe
July 2001,
Bioorganic & medicinal chemistry letters,
R H Peters, and
D F Crowe, and
M A Avery, and
W K Chong, and
M Tanabe
May 1975,
Journal of pharmaceutical sciences,
R H Peters, and
D F Crowe, and
M A Avery, and
W K Chong, and
M Tanabe
April 1975,
Journal of pharmaceutical sciences,
R H Peters, and
D F Crowe, and
M A Avery, and
W K Chong, and
M Tanabe
December 1972,
Journal of reproduction and fertility,
