4.4 Article

Construction of pyrrolophenanthridinone scaffolds mediated by samarium(II) diiodide and access to natural product synthesis

期刊

TETRAHEDRON
卷 71, 期 34, 页码 5513-5519

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2015.06.067

关键词

Radical cyclization; Heterocycles; Pyrrolophenanthridinone scaffolds; Samarium diiodide

资金

  1. Strategic Research Foundation from the Ministry of Education, Culture, Sports, Science, and Technology of Japan (MEXT) [S0801063]
  2. Kyoto Pharmaceutical University Fund for the Promotion of Scientific Research

向作者/读者索取更多资源

Pyrrolophenanthridinone derivatives including the natural products were readily synthesized by samarium(II)-mediated reductive cyclization of aryl radical onto a benzene ring under mild reaction conditions. This methodology was applied to the concise synthesis of anhydrolycorinone, a natural pyrrolophenanthridinone and a precursor of hippadine and anhydrolycorine. (C) 2015 Elsevier Ltd. All rights reserved.

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