16α-Hydroxy Steroids

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Rearrangement of 14/3-Hydroxy-12ß-sulfoxy-steroids to 13,17-Seco-12,17-cyclo-steroids; a 2D-NMR Analysis

During our work on cardiaoctive steroids we studied the elimination of the 12/3-sulfoxy-group. It is well known that 12/J-tosyloxyor 12/3-mesyloxysteroids with C/D-trans juncture undergo elimination to yield C-nor-D-homo steroids with 12(13) or 13(18) double bonds [1—6]. The same rearrangement product was obtained by the reaction of a 12/3-tosyloxycardenolide [7] with C/D-eis juncture. No GrobF...

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ژورنال

عنوان ژورنال: Journal of Biological Chemistry

سال: 1960

ISSN: 0021-9258

DOI: 10.1016/s0021-9258(18)69461-x