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One-pot synthesis and property study on thieno[3,2-b]furan compounds

机译:Thieno的一壶合成及性质研究[3,2-B]呋喃化合物

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摘要

Based on the regioselective intermolecular Suzuki coupling and subsequent intramolecular Ullmann C-O coupling reactions, one-pot synthesis of benzo[4,5]thieno[3,2-b]benzofurans (BTBFs) was developed after optimization of the reaction conditions including catalysts, solvents, bases, ligands and reaction times. The one-pot reaction, with only 2 mol% Pd(PPh3)(4) and 2 mol% copper(i) thiophene-2-carboxylate (CuTc) as the catalysts, K(3)PO(4)3H(2)O as the base and tert-butanol as the solvent, afforded moderate to good yields (up to 70%) for a variety of substrates.
机译:基于区域选择性分子间铃木偶联和随后的分子内ullmann CO偶联反应,在优化包括催化剂,溶剂的反应条件下,开发了苯并[4,5]噻吩并[3,2-B]苯并呋喃(BTBFS)的一锅合成 ,碱,配体和反应时间。 单罐反应,仅用2摩尔%Pd(PPH3)(4)和2mol%铜(I)噻吩-2-羧酸盐(Cutc)作为催化剂,K(3)PO(4)3H(2) o作为碱和叔丁醇作为溶剂,得到中等的产率(高达70%)的各种基材。

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  • 来源
    《RSC Advances》 |2019年第13期|共5页
  • 作者单位

    Univ Chinese Acad Sci Sch Chem Sci Beijing 100049 Peoples R China;

    Univ Chinese Acad Sci Sch Chem Sci Beijing 100049 Peoples R China;

    Univ Chinese Acad Sci Sch Chem Sci Beijing 100049 Peoples R China;

    Univ Chinese Acad Sci Sch Chem Sci Beijing 100049 Peoples R China;

    Univ Chinese Acad Sci Sch Chem Sci Beijing 100049 Peoples R China;

    Univ Chinese Acad Sci Sch Chem Sci Beijing 100049 Peoples R China;

    Chinese Acad Sci Beijig Natl Lab Mol Sci CAS Key Lab Organ Solids Inst Chem Beijing 100190 Peoples R China;

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  • 正文语种 eng
  • 中图分类 化学;
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