4.4 Article

Concise total syntheses of Marinoquinolines A-C

期刊

TETRAHEDRON LETTERS
卷 53, 期 10, 页码 1271-1274

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2011.12.124

关键词

Total synthesis; Natural product; Marinoquinoline; Pyrroloquinoline; Antitumor

资金

  1. NCET
  2. Fok Ying Tong Education Foundation [121040]
  3. Ministry of Education of China [2009ZX09103-128]
  4. Fundamental Research Funds for the Central Universities [JKZ2009002, JKGZ201110]

向作者/读者索取更多资源

The first concise total syntheses of pyrroloquinoline natural products, Marinoquinolines A-C, have been achieved in six linear steps from commercially available starting materials. The key steps were a reaction between (p-tolylsulfonyl)methylisocyanide (TosMIC) and alpha, beta-unsaturated ester under basic condition to prepare the pyrrole moiety and Morgen-Walls reaction to construct quinoline ring. (C) 2012 Elsevier Ltd. All rights reserved.

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