An approach to the construction of the aromatic portions of naphthomycin and the rubradirins - nucleophilic additions to unsymmetrically substituted naphthoquinones

Alan P. Kozikowski, Kiyoshi Sugiyama, James P. Springer

Research output: Contribution to journalArticlepeer-review

Abstract

A Diels-Alder entry into the highly substituted naphthoquinones present in the rubradirins and naphthomycin is described.

Original languageEnglish (US)
Pages (from-to)3257-3260
Number of pages4
JournalTetrahedron Letters
Volume21
Issue number34
DOIs
StatePublished - 1980

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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