Stereoselective synthesis of zoanthenol ABC-ring by radical strategy

Shuji Yamashita, Naoki Suda, Yujiro Hayashi, Masahiro Hirama

Research output: Contribution to journalArticlepeer-review

16 Citations (Scopus)


Zoanthenol, isolated from Zoanthus sp., possesses an extremely complex architecture including congested quaternary carbons. We describe a concise synthesis of the fully functionalized ABC-ring of zoanthenol based on sequential radical reactions.

Original languageEnglish
Pages (from-to)1389-1391
Number of pages3
JournalTetrahedron Letters
Issue number11
Publication statusPublished - 2013 Mar 13


  • Atom transfer
  • Marine natural product
  • Tandem radical cyclization
  • Zoanthenol

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry


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