Steroids p. 697 - 702 (1996)
Update date:2022-09-26
Topics:
Vincze, Iren
Hackler, Laszlo
Szendi, Zsuzsa
Schneider, Gyula
Aminosteroids were prepared and acylated with protected amino acids by means of the mixed anhydride or the active ester method. The tert- butyloxycarbonyl-(BOC) protecting group was eliminated by acidolysis, and the benzyloxycarbonyl-(Z) group by catalytic hydrogenation. 3β- and 6β- Glycylamidosteroids were prepared by indirect amination of chloroacetamido derivatives, formed by the Ritter reaction on the corresponding 3α,5α- cyclo and 5α,6α-epoxy steroids. Water soluble double salts were produced from the compounds for pharmacological investigations.
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