Novel trinitrogen-containing triheterocycles via the intramolecular nitrile oxide cycloaddition reaction

Andrew J. Ferreira, Danielle M. Solano, James S. Oakdale, Mark J. Kurth

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

The intramolecular nitrile oxide cycloaddition (INOC) reaction is applied to the synthesis of novel isoxazolooxazepinoindazole, benzoisoxazolodiazepinoindazolone, and spiro[isoxazoloazepine]piperidine heterocycles. Each of these targets incorporates a unique trinitrogen-containing triheterocyclic framework.

Original languageEnglish (US)
Article numberM68111SS
Pages (from-to)3241-3246
Number of pages6
JournalSynthesis
Issue number20
DOIs
StatePublished - 2011

Fingerprint

Nitriles
Cycloaddition
Oxides
piperidine

Keywords

  • alkenes
  • cycloadditions
  • heterocycles
  • pericyclic reactions
  • spiro compounds

ASJC Scopus subject areas

  • Organic Chemistry
  • Catalysis

Cite this

Ferreira, A. J., Solano, D. M., Oakdale, J. S., & Kurth, M. J. (2011). Novel trinitrogen-containing triheterocycles via the intramolecular nitrile oxide cycloaddition reaction. Synthesis, (20), 3241-3246. [M68111SS]. https://doi.org/10.1055/s-0030-1260188

Novel trinitrogen-containing triheterocycles via the intramolecular nitrile oxide cycloaddition reaction. / Ferreira, Andrew J.; Solano, Danielle M.; Oakdale, James S.; Kurth, Mark J.

In: Synthesis, No. 20, M68111SS, 2011, p. 3241-3246.

Research output: Contribution to journalArticle

Ferreira, Andrew J. ; Solano, Danielle M. ; Oakdale, James S. ; Kurth, Mark J. / Novel trinitrogen-containing triheterocycles via the intramolecular nitrile oxide cycloaddition reaction. In: Synthesis. 2011 ; No. 20. pp. 3241-3246.
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