A cascade radical-mediated macrocyclisation–transannulation approach to oestrogen steroids

Miguel Angel González Cardente, Stuart McCulloch, Gerald Pattenden
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Abstract

A new approach to ring A aromatic steroids, based on cascade 13-endo-trig/dig macrocyclisations followed by sequential 5-exo-trig and 6-exo-trig transannulations, exemplified in the syntheses of the cis,anti,trans tetracycle 9 and the trans,syn tetracycle 13 from the ortho-substituted aryl polyen(yne) precursors, 8 and 12 respectively, is described.

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级联自由基介导的雌激素类固醇大环化-环化途径
本文描述了一种基于级联13-内三角/dig大环化,然后依次进行5-外三角和6-外三角环化的环A芳香甾体的新方法,该方法分别由邻位取代芳基聚烯(yne)前体8和12合成顺式,反式,反式,反式,反式四环9和反式,syn四环13。
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