1985
DOI: 10.1007/bf00811255
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Zur Stereochemie der Vitamin D3-Epoxide R�ntgenstrukturanalyse einer 5,6-7,8-10,19-Triepoxidverbindung

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“…The reaction of oestrone 2-hydroxyethyl ether (1 32) with isocyanuric chloride, N-chlorosuccinimide, or ethyl chloroiminocarbonate gives 10~-chloro-3,3-ethylenedioxyoestra-1,4dien-17-one (133); the yield is improved if the reaction occurs in the presence of various alcoholsprobably through the formation of mixed ketals. Removal of the protecting group with acid and reaction of the ketone with calcium carbonate in dimethylformamide then yields 9,ll -didehydro-oestrone (1 34)…”
Section: Androstanes and Oestranesmentioning
confidence: 99%
“…The reaction of oestrone 2-hydroxyethyl ether (1 32) with isocyanuric chloride, N-chlorosuccinimide, or ethyl chloroiminocarbonate gives 10~-chloro-3,3-ethylenedioxyoestra-1,4dien-17-one (133); the yield is improved if the reaction occurs in the presence of various alcoholsprobably through the formation of mixed ketals. Removal of the protecting group with acid and reaction of the ketone with calcium carbonate in dimethylformamide then yields 9,ll -didehydro-oestrone (1 34)…”
Section: Androstanes and Oestranesmentioning
confidence: 99%