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Furyl intermediates of cardenolides, their synthesis and production of cardenolides and their isomers therefrom

机译:心内酯的呋喃基中间体,及其合成和生产心内酯及其异构体

摘要

The invention relates to furyl intermediates useful in the preparation of synthetic cardenolides and their isomers, to the preparation thereof, and to the conversion of such intermediates into cardenolides. The process provides for the reaction of an unsaturated steroidal 17-ketone with an alkali or alkaline earth metal p-furyl compound to produce an allylic alcohol which is subjected to acetylation and allylic rearrangement. The resulting material is then hydrogenated to produce the furyl intermediate. Cardenolides are formed therefrom by oxidation of the furyl intermediates.
机译:呋喃基中间体本发明涉及可用于制备合成的烯醇内酯及其异构体的呋喃基中间体,涉及其制备,以及将这类中间体转化为烯醇内酯的方法。该方法提供了不饱和甾族17-酮与碱金属或碱土金属对-呋喃基化合物的反应,以产生烯丙基醇,将其进行乙酰化和烯丙基重排。然后将所得材料氢化以产生呋喃基中间体。通过呋喃基中间体的氧化从中形成吗啉化物。

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