Diels-alder reactions of 2H-thiopyrans

Dale E. Ward, Wajdi M. Zoghaib, Chung K. Rhee, Gai Yuanzhu

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

Oxygenated 2H-thiopyrans react with typical dienophiles to produce predominantly endo adducts in modest to high yield. The adducts can be desulfurized to give compounds equivalent to a Diels-Alder adduct of a cis -diene.

Original languageEnglish
Pages (from-to)845-848
Number of pages4
JournalTetrahedron Letters
Volume31
Issue number6
DOIs
Publication statusPublished - 1990

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Cycloaddition Reaction
thiopyran

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Diels-alder reactions of 2H-thiopyrans. / Ward, Dale E.; Zoghaib, Wajdi M.; Rhee, Chung K.; Yuanzhu, Gai.

In: Tetrahedron Letters, Vol. 31, No. 6, 1990, p. 845-848.

Research output: Contribution to journalArticle

Ward, Dale E. ; Zoghaib, Wajdi M. ; Rhee, Chung K. ; Yuanzhu, Gai. / Diels-alder reactions of 2H-thiopyrans. In: Tetrahedron Letters. 1990 ; Vol. 31, No. 6. pp. 845-848.
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