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

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Fingerprint Dive into the research topics of 'Diels-alder reactions of 2H-thiopyrans'. Together they form a unique fingerprint.

  • Cite this