Studies directed toward the total synthesis of the rubradirin antibiotics. 4. A new Diels-Alder-Claisen effective diene

Alan P. Kozikowski, Kiyoshi Sugiyama, Edward Huie

Research output: Contribution to journalArticle

Abstract

A new diene has been synthesized which effectively couples the Diels-Alder reaction with the Claisen rearrangement.

Original languageEnglish (US)
Pages (from-to)3381-3384
Number of pages4
JournalTetrahedron Letters
Volume22
Issue number35
DOIs
StatePublished - 1981
Externally publishedYes

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Cycloaddition Reaction
Anti-Bacterial Agents
rubradirin

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Studies directed toward the total synthesis of the rubradirin antibiotics. 4. A new Diels-Alder-Claisen effective diene. / Kozikowski, Alan P.; Sugiyama, Kiyoshi; Huie, Edward.

In: Tetrahedron Letters, Vol. 22, No. 35, 1981, p. 3381-3384.

Research output: Contribution to journalArticle

Kozikowski, Alan P. ; Sugiyama, Kiyoshi ; Huie, Edward. / Studies directed toward the total synthesis of the rubradirin antibiotics. 4. A new Diels-Alder-Claisen effective diene. In: Tetrahedron Letters. 1981 ; Vol. 22, No. 35. pp. 3381-3384.
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