首页> 外文期刊>RSC Advances >Synthetic studies en route to the first total synthesis of a naturally occurring quinone from Acorus gramineus, iso-merrilliaquinone, iso-magnoshinin and 2-epi-3,4-dihydro magnoshinin
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Synthetic studies en route to the first total synthesis of a naturally occurring quinone from Acorus gramineus, iso-merrilliaquinone, iso-magnoshinin and 2-epi-3,4-dihydro magnoshinin

机译:合成研究正在进行了从 Acorus gramineus ,异美林醌,iso-magnoshinin和2- epi -3,4-dihydro magnoshinin天然合成醌的首次合成

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摘要

A unified synthetic strategy based on [4 + 2] cycloaddition of readily accessible coupling fragments was conceptualized for the racemic total synthesis of recently isolated bioactive merrilliaquinone and other closely related quinones such as gramineusquinone B as well as neolignan, magnoshinin. The present article discloses our efforts in this direction which culminated in the total syntheses of gramineusquinone B, iso-merrilliaquinone, iso-magnoshinin and 2-epi-3,4-dihydro magnoshinin.
机译:为易于分离的生物活性美林醌和其他紧密相关的醌(如禾谷胺醌B和新木脂,厚朴素)的外消旋全合成构想了一种基于[4 + 2]环加成的容易获得的偶联片段的统一合成策略。本文公开了我们在这个方向上所做的努力,最终合成了禾谷胺醌B,异美林醌,异木香精和2- -3,4-二氢厚朴素。

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