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首页> 外文期刊>Organic letters >Phosphine-catalyzed domino reaction: Highly stereoselective synthesis of trans-2,3-dihydrobenzofurans from salicyl n-thiophosphinyl imines and allylic carbonates
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Phosphine-catalyzed domino reaction: Highly stereoselective synthesis of trans-2,3-dihydrobenzofurans from salicyl n-thiophosphinyl imines and allylic carbonates

机译:膦催化的多米诺反应:由水杨基正硫代次膦亚胺和烯丙基碳酸酯高度立体选择性地合成反式2,3-二氢苯并呋喃

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摘要

A novel phosphine-catalyzed domino reaction of salicyl N-thiophosphinyl imines and allylic carbonates was developed. The allylic carbonate, in this reaction, serves as a new kind of 1,1-dipolar synthon. This method offered a powerful approach to the construction of a highly substituted trans-2,3-dihydrobenzofuran skeleton with high diastereoselectivity.
机译:开发了一种新的膦催化的水杨基N-硫代次膦亚胺和烯丙基碳酸酯的多米诺骨牌反应。在该反应中,碳酸烯丙酯用作新型的1,1-偶极合成子。该方法为构建具有高非对映选择性的高度取代的反式2,3-二氢苯并呋喃骨架提供了有力的方法。

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