Tandem Reactions of 1,2,4-Oxadiazoleswith Allylamines

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13 Citations (Scopus)

Abstract

A reaction of 3-chloro-1,2,4-oxadiazoles with allylamine and diallylamine has been investigated. 3,3a,4,5-Tetrahydroisoxazolo[3,4-d]pyrimidinesare produced through a tandem ANRORC/[3þ2]cycloaddition pathway consisting of the addition of allylamine to the 1,2,4-oxadiazole, followed byring opening, nitrone formation, and finally cycloaddition. 3-N-Allylamino-1,2,4-oxadiazoles were also obtained as minor products through aclassical SNAr. Conversely, a reaction with diallylamine produces 3-N,N-diallylamino-1,2,4-oxadiazole and imidazoline through tandem SNAr/aziridination and nucleophilic ring opening.
Original languageEnglish
Pages (from-to)4749-4751
Number of pages3
JournalOrganic Letters
Volume13
Publication statusPublished - 2011

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

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