Synthesis and 1,3-dipolar cycloadditions of a new enantiopure cyclic nitrone

Ramón Alibés, Pilar Blanco, Pedro De March, Marta Figueredo, Josep Font, Ángel Álvarez-Larena, Juan F. Piniella

Research output: Contribution to journalArticleResearchpeer-review

33 Citations (Scopus)


A new enantiopure cyclic nitrone has been efficiently synthesized from a D-glyceraldehyde derivative. Its 1,3-dipolar cycloaddition to different classes of dipolarophiles show complete antifacial selectivity, furnishing highly functionalized enantiopure bicyclic isoxazolidines. © 2002 Elsevier Science Ltd. All rights reserved.
Original languageEnglish
Pages (from-to)523-525
JournalTetrahedron Letters
Issue number3
Publication statusPublished - 13 Jan 2003


  • Dipolar cycloaddition
  • Enantiopure cyclic nitrone
  • Facial selectivity


Dive into the research topics of 'Synthesis and 1,3-dipolar cycloadditions of a new enantiopure cyclic nitrone'. Together they form a unique fingerprint.

Cite this