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乌尔曼型分子内 C-O 反应合成六元并噻吩[3,2-b]呋喃衍生物

Ullmann-Type Intramolecular C-O Reaction Toward Thieno[3,2-b]furan Derivatives with up to Six Fused Rings.

机构信息

School of Chemistry and Chemical Engineering, University of Chinese Academy of Sciences , Beijing 100049, P. R. China.

Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences , Beijing 100190, P. R. China.

出版信息

J Org Chem. 2017 Oct 20;82(20):10920-10927. doi: 10.1021/acs.joc.7b01745. Epub 2017 Sep 28.

Abstract

A new strategy for the efficient synthesis of thieno[3,2-b]benzofuran derivatives (15 examples) was achieved on the basis of successive regioselective intermolecular Suzuki and newly developed intramolecular Ullmann C-O reactions in up to a 70% overall yield. The fast intramolecular C-O reaction can be realized by an efficient catalytic combination of CuI/1,10-phenanthroline in up to a 97% yield. This method is suitable for the construction of highly fused thieno[3,2-b]furan-containing heterocycles including DTBDF and TTDBF. The π-π and hydrogen-bonding interactions observed for the C-DTBDF single crystal suggest its great potential for OFET applications in the near future.

摘要

一种高效合成噻吩并[3,2-b]苯并呋喃衍生物(15 个实例)的新策略是基于连续的区域选择性的Suzuki 反应和新开发的分子内Ullmann C-O 反应,总收率高达 70%。通过高效的催化组合 CuI/1,10-菲咯啉,快速的分子内 C-O 反应可以实现高达 97%的产率。该方法适用于高度稠合的噻吩并[3,2-b]呋喃杂环的构建,包括 DTBDF 和 TTDBF。C-DTBDF 单晶中观察到的π-π和氢键相互作用表明其在不久的将来在 OFET 应用中有很大的潜力。

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