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Nitrones and oxaziridines. XLVI. Formation of pyrrolo[3, 2, 1-ij]quinolines by intramolecular nitrone cycloaddition

Journal Article


Abstract


  • Intramolecular 1, 3-dipolar cycloaddition occurs between nitrones derived from indole-7-carbaldehydes and adjacent allylic substituents on the indole nitrogen atoms. The resulting pyrroloquinoline derivatives (4a-i) have been characterized fully. A range of other potential precursors to cycloaddition reactions have been synthesized, but cyclization sequences have not been completed. © 1993 ASEG.

Publication Date


  • 1993

Citation


  • Black, D. S. C., Keller, P. A., & Kumar, N. (1993). Nitrones and oxaziridines. XLVI. Formation of pyrrolo[3, 2, 1-ij]quinolines by intramolecular nitrone cycloaddition. Australian Journal of Chemistry, 46(6), 843-862. doi:10.1071/CH9930843

Scopus Eid


  • 2-s2.0-84970614001

Start Page


  • 843

End Page


  • 862

Volume


  • 46

Issue


  • 6

Abstract


  • Intramolecular 1, 3-dipolar cycloaddition occurs between nitrones derived from indole-7-carbaldehydes and adjacent allylic substituents on the indole nitrogen atoms. The resulting pyrroloquinoline derivatives (4a-i) have been characterized fully. A range of other potential precursors to cycloaddition reactions have been synthesized, but cyclization sequences have not been completed. © 1993 ASEG.

Publication Date


  • 1993

Citation


  • Black, D. S. C., Keller, P. A., & Kumar, N. (1993). Nitrones and oxaziridines. XLVI. Formation of pyrrolo[3, 2, 1-ij]quinolines by intramolecular nitrone cycloaddition. Australian Journal of Chemistry, 46(6), 843-862. doi:10.1071/CH9930843

Scopus Eid


  • 2-s2.0-84970614001

Start Page


  • 843

End Page


  • 862

Volume


  • 46

Issue


  • 6