首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Iron-catalyzed tandem carbon-carbon/carbon-oxygen bond formation/aromatization of 2 '-alkynyl-biphenyl-2-carbinols: a new approach to the synthesis of substituted phenanthrenes
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Iron-catalyzed tandem carbon-carbon/carbon-oxygen bond formation/aromatization of 2 '-alkynyl-biphenyl-2-carbinols: a new approach to the synthesis of substituted phenanthrenes

机译:铁催化的串联碳-碳/碳-氧键形成/芳香化的2'-炔基-联苯-2-甲醇:合成取代菲的新方法

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摘要

An iron-catalyzed efficient synthesis of substituted phenanthrenes through tandem intramolecular C-C/C-O bond formations/aromatization of 2'-alkynyl-biphenyl-2-carbinols is reported. This method provides a novel, highly efficient, and straightforward route to 9,10-substituted phenanthrene in good to excellent yields. The present strategy involves tandem Fe(OTf)(3)-catalyzed generation of benzylic carbocation, 6-exo-dig cyclization of alkyne, carbon-oxygen bond formation, and aromatization steps in one pot. (C) 2014 Elsevier Ltd. All rights reserved.
机译:通过串联分子内C-C / C-O键形成/ 2'-炔基-联苯-2-甲醇的芳香化反应,铁催化了取代菲的高效合成。该方法提供了一种新颖,高效且直接的途径,可以以良好的产率获得9,10取代的菲。本策略涉及串联Fe(OTf)(3)催化生成苄基碳正离子,炔烃的6-exo-dig环化,碳-氧键形成和一锅中的芳构化步骤。 (C)2014 Elsevier Ltd.保留所有权利。

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