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Unusual Wagner-Meerwein rearrangement in the denitroamination of steroidal 20R-nitroamines: crystal structure of 17α-methyl-12a-methylene-c(12a)-homo-18-nor-(13S)-androst-5-en-3β-yl acetate

AutorFreire, Raimundo ; Salazar, José A.; Suárez, Ernesto ; Betancor, Carmen; Melián, Daniel; Prangé, Thierry; Pascard, Claudine
Fecha de publicación1985
EditorTurpin Distribution
CitaciónJournal of Chemical Research(S) 1985: 152-153 (1985)
ResumenIn previous papers we have reported that treatment of several steroidal nitroamines with acetic anhydride and pyridine leads to nitrogen free-products. In the study of the denitroamination of the (20R)-nitroaminopregnane derivative (1) we found that, in addition to substitution and β-hydrogen elimination products, the arearranged compounds (2) and (4) were formed.
Descripción2 pages, 1 figure, 1 scheme.-- Supplementary material available in full-text paper in Journal of Chemical Research(M), http://hdl.handle.net/10261/17594
URIhttp://hdl.handle.net/10261/17595
ISSN0308-2350
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