4.5 Article

Synthesis of 5-(2-methoxy-1-naphthyl)-and 5-[2-(methoxymethyl)-1-naphthyl]-11H-benzo[b]fluorene as 2,2′-disubstituted 1,1′-binaphthyls via benzannulated enyne-allenes

期刊

BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
卷 7, 期 -, 页码 496-502

出版社

BEILSTEIN-INSTITUT
DOI: 10.3762/bjoc.7.58

关键词

benzannulated enediynyl alcohols; benzannulated enyne-allenes; 2,2 '-disubstituted 1,1 '-binaphthyls; 5-(1-naphthyl)-11H-benzo[b]fluorenes; Schmittel cascade cyclizations

资金

  1. National Science Foundation [CHE-0909613, CHE-9120098]
  2. NSF-EPSCoR [1002165R]
  3. Direct For Mathematical & Physical Scien [0909613] Funding Source: National Science Foundation
  4. Division Of Chemistry [0909613] Funding Source: National Science Foundation

向作者/读者索取更多资源

5-(2-Methoxy-1-naphthyl)-and 5-[2-(methoxymethyl)-1-naphthyl]-11H-benzo[b]fluorene were synthesized by treatment of the corresponding benzannulated enediynes with potassium tert-butoxide in refluxing toluene to give benzannulated enyne-allenes for the subsequent Schmittel cascade cyclization reactions. The structures of these two 5-(1-naphthyl)-11H-benzo[b]fluorenes could be regarded as 2,2'-disubstituted 1,1'-binaphthyls with the newly constructed benzofluorenyl group serving as a naphthyl moiety.

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