4.4 Article

A facile two-step synthesis of thiophene end-capped aromatic systems

期刊

TETRAHEDRON LETTERS
卷 53, 期 14, 页码 1816-1818

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2012.01.122

关键词

Naphthodithiophene; Nucleophilic aromatic substitution; Oxygen-sulfur replacement; Sulfur-containing aromatic heterocycles; Thiophene

资金

  1. National Synchrotron Research Center [2-2549/PS01]
  2. Royal Golden Jubilee (RGJ) program
  3. Development and Promotion of Science and Technology Talents (DPST)
  4. Center of Excellence for Innovation in Chemistry (PERCH-CIC)
  5. Thailand Graduate Institute of Science and Technology (TGIST)

向作者/读者索取更多资源

Thiophene end-capped aromatic analogues, that is, naphthothiophenes, naphthodithiophenes, pyrenothiophene, and benzotrithiophene, can be prepared from commercially available hydroxyarenes in two steps, including (1) a consecutive acid-mediated nucleophilic aromatic substitution of hydroxyarenes with 2-mercaptoethanol, followed by cyclization to form an arene-fused dihydrothiophene, and (2) oxidation of the dihydrothiophene unit to thiophene. (C) 2012 Elsevier Ltd. All rights reserved.

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