NITRONES AND OXAZIRIDINES .46. FORMATION OF PYRROLO[3,2,1-IJ]QUINOLINES BY INTRAMOLECULAR NITRONE CYCLOADDITION

Authors
BLACK DS KELLER PA KUMAR N
Citation
Ds. Black et al., NITRONES AND OXAZIRIDINES .46. FORMATION OF PYRROLO[3,2,1-IJ]QUINOLINES BY INTRAMOLECULAR NITRONE CYCLOADDITION, Australian Journal of Chemistry, 46(6), 1993, pp. 843-862
Citations number
16
Categorie Soggetti
Chemistry
Journal title
Australian Journal of Chemistry → ACNP
ISSN journal
00049425
Volume
46
Issue
6
Year of publication
1993
Pages
843 - 862
Database
ISI
SICI code
0004-9425(1993)46:6<843:NAO.FO>2.0.ZU;2-G
Abstract
Intramolecular 1,3-dipolar cycloaddition occurs between nitrones deriv ed from indole-7-carbaldehydes and adjacent allylic substituents on th e indole nitrogen atoms. The resulting pyrroloquinoline derivatives (4 a-i) have been characterized fully. A range of other potential precurs ors to cycloaddition reactions have been synthesized, but cyclization Sequences have not been completed.