4.5 Article

One-Pot Synthesis of Diazine-Bridged Bisindoles and Concise Synthesis of the Marine Alkaloid Hyrtinadine A

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2011, 期 24, 页码 4532-4535

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201100680

关键词

Alkaloids; Arylation; Boron; C-C coupling; Multicomponent reactions; Palladium

资金

  1. Merck KGaA
  2. Darmstadt
  3. Fonds der Chemischen Industrie

向作者/读者索取更多资源

Diazine-bridged bisindoles are readily obtained from N-Boc-protected 3-iodoindoles and 3-iodo-7-azaindole in a pseudo three-component reaction involving a one-pot Masuda borylation-Suzuki arylation sequence. Some of the title compounds display promising cytotoxic properties. The versatility of this methodology is illustrated by a very concise total synthesis of the marine alkaloid hyrtinadine A.

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