A convergent total synthesis of the marine sponge alkaloid ageladine A via a strategic 6π-2-azatriene electrocyclization

Matthew L. Meketa, Steven M. Weinreb

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

A second generation total synthesis of the marine sponge metabolite ageladine A utilizing a biogenetically inspired 6π-2-azaelectrocyclization of triene 34 as the key step is performed to construct the imidazopyridine core of the metabolite.

Original languageEnglish (US)
Pages (from-to)9112-9119
Number of pages8
JournalTetrahedron
Volume63
Issue number37
DOIs
StatePublished - Sep 10 2007

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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