4.3 Article

Facile Synthesis and Lateral π-Expansion of Bisanthenes

期刊

CHEMISTRY LETTERS
卷 42, 期 6, 页码 592-594

出版社

CHEMICAL SOC JAPAN
DOI: 10.1246/cl.130153

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资金

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan [2105]
  2. ALCA Program of the Japan Science and Technology Agency (JST)
  3. JSPS
  4. Grants-in-Aid for Scientific Research [25620057, 23550053, 24550049, 25248007, 21106014] Funding Source: KAKEN

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The improved Scholl reaction allows for the direct cyclization of anthracene oligomers to give bisanthene, teranthene, and quateranthene. Furthermore, a variety of pi-expanded bisanthenes are obtained by the Diels-Alder cycloaddition of bisanthene with several arynes. These reactions would allow us to synthesize various size- and shape-controlled polyperiacenes.

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