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通过杂芳醇的自身缩合和分子内 Friedel-Crafts 型反应合成二芳基和三芳基烷烃。

Di- and triheteroarylalkanes via self-condensation and intramolecular Friedel-Crafts type reaction of heteroaryl alcohols.

机构信息

Department of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Mohali, Sector 81, S A S Nagar, Manuali PO, Punjab 140 306, India.

出版信息

Org Biomol Chem. 2013 Dec 14;11(46):8030-5. doi: 10.1039/c3ob41945b.

Abstract

An efficient synthetic approach to diheteroarylmethanes and 1,3-diheteroarylpropenes has been developed via Yb(III)-catalyzed sequential self-condensation of 2-furfuryl (or 2-thienyl or 3-indolyl) alcohols followed by intramolecular Friedel-Crafts type reaction and elimination of an aldehyde. This method offers a powerful entry and a potential alternative to the traditional synthesis of diheteroarylalkanes, which are precursors to the synthesis of several intriguing heteroaryls and more significantly, to the synthesis of biofuels.

摘要

通过 Yb(III)催化的 2-糠基(或 2-噻吩基或 3-吲哚基)醇的顺序自缩合,然后进行分子内 Friedel-Crafts 型反应和醛消除,开发了一种高效合成二芳基甲烷和 1,3-二芳基丙烯的方法。该方法为传统的二芳基烷烃合成提供了有力的途径和潜在的替代方法,二芳基烷烃是合成多种有趣的杂芳环的前体,更重要的是,是合成生物燃料的前体。

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