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首页> 外文期刊>Chemistry: A European journal >Asymmetric Synthesis of 2,3-Dihydrobenzofurans by a [4+1] Annulation Between Ammonium Ylides and In Situ Generated o-Quinone Methides
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Asymmetric Synthesis of 2,3-Dihydrobenzofurans by a [4+1] Annulation Between Ammonium Ylides and In Situ Generated o-Quinone Methides

机译:2,3-二氢苯并呋喃的不对称合成[4 + 1]环核和原位产生的O-醌甲基化物

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摘要

A highly enantio- and diastereoselective [4+1] annulation between in situ generated ammonium ylides and oquinone methides for the synthesis of a variety of 2,3-dihydrobenzofurans has been developed. The key factors controlling the reactivity and stereoselectivity were systematically investigated by experimental and computational means and the energy profiles obtained provide a deeper insight into the mechanistic details of this reaction.
机译:已经开发出在原位产生的铵y型y型氧化钇和oquinone甲基化合物之间进行高度抗映的和非对映选择性[4 + 1]环,用于合成各种2,3-二氢呋喃脲。 通过实验和计算装置系统地研究了控制反应性和立体选择性的关键因素,并且获得的能量谱提供了更深入的了解该反应的机械细节。

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