Title: 20-Hydroxyimino-5 alpha-pregna-9(11),16-dien-3 beta-yl acetate and 17-oxo-5 alpha-androst-9(11)-en-3 beta-yl acetate
Authors: Novoa de Armas, Hector ×
Peeters, Oswald
Blaton, Norbert
De Ranter, Camiel
Garcia, JAR
Moreno, MR
Ginarte, YMA #
Issue Date: Dec-2000
Publisher: Munksgaard int publ ltd
Series Title: Acta crystallographica section c-crystal structure communications vol:56 pages:E582-E583
Abstract: In the title compounds, C23H33NO3 and C21H30O3, respectively, the ester linkage in ring A is equatorial. In these steroids, the six-membered rings A and B have chair conformations, but ring C can be better described as a half-chair. The five-membered ring D adopts a 14 alpha -envelop conformation. The A/B, B/C and C/D ring junctions are trans.
ISSN: 2053-2296
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Biocrystallography
× corresponding author
# (joint) last author

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