4.5 Article

Metal-Free Oxidative Coupling Reactions via σ-Iodonium Intermediates: The Efficient Synthesis of Bithiophenes Using Hypervalent Iodine Reagents

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2011, 期 31, 页码 6326-6334

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201100969

关键词

Iodine; Cross-coupling; Biaryls; Sulfur heterocycles; Oligomerization

资金

  1. Japan Society for the Promotion of Science (JSPS)
  2. New Energy and Industrial Technology Development Organization (NEDO) of Japan
  3. Ritsumeikan Global Innovation Research Organization (R-GIRO)
  4. Grants-in-Aid for Scientific Research [21249002, 11J09317] Funding Source: KAKEN

向作者/读者索取更多资源

The direct oxidative biaryl coupling reaction is an attractive tool for environmentally benign green chemistry. A novel direct method for the synthesis of bithiophene using a hyper-valent iodine reagent has been developed. The reaction mechanism has also been investigated, casting light on the reaction intermediate and revealing the reactivity with iodonium salts.

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