618457-34-4Relevant academic research and scientific papers
Stereoselective halogenation of the 16-hydroxymethyl-3-methoxy-13α-estra-1,3,5(10)-trien-17-ols and their solvolytic investigation
Woelfling, Janos,Mernyak, Erzsebet,Forgo, Peter,Schneider, Gyula
, p. 451 - 458 (2007/10/03)
The primary hydroxy functions of 16α-hydroxymethyl-3-methoxy-13α-estra-1,3,5(10)-trien-17β-ol (3a) and 16β-hydroxymethyl-3-methoxy-13α-estra-1,3,5(10)-trien-17α-ol (4a) were stereoselectively transformed into good leaving groups. On alkaline methanolysis of the 16-halomethyl or 16-tolylsulfonyloxymethyl derivatives, a new D-seco-13α-estrone derivative was obtained in high yield.
