In:
Zeitschrift für Naturforschung B, Walter de Gruyter GmbH, Vol. 40, No. 5 ( 1985-5-1), p. 656-660
Abstract:
The rearrangement of 3-oxo-14β-hydroxy-12β-methanesulfoxy-card-20(22)-enolide and 14β-hydroxy-12β-methanesulfoxy-pregnane-3,20-dione during elimination of the sulfoxygroups was studied. By means of 2D-NMR analysis the structures were determined as 13,17-seco-12,17-cyclo-steroids.
Type of Medium:
Online Resource
ISSN:
1865-7117
,
0932-0776
DOI:
10.1515/znb-1985-0516
Language:
English
Publisher:
Walter de Gruyter GmbH
Publication Date:
1985
detail.hit.zdb_id:
2078109-X
detail.hit.zdb_id:
124635-5
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