An intramolecular azomethine ylide-alkene cycloaddition approach to pyrrolo[3,2-c]quinolines-synthesis of a C2-truncated martinelline model

Authors
Mahmud, H Lovely, CJ Dias, HVR
Citation
H. Mahmud et al., An intramolecular azomethine ylide-alkene cycloaddition approach to pyrrolo[3,2-c]quinolines-synthesis of a C2-truncated martinelline model, TETRAHEDRON, 57(19), 2001, pp. 4095-4105
Citations number
28
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON
ISSN journal
00404020 → ACNP
Volume
57
Issue
19
Year of publication
2001
Pages
4095 - 4105
Database
ISI
SICI code
0040-4020(20010507)57:19<4095:AIAYCA>2.0.ZU;2-L
Abstract
The hexahydropyrrolo[3,2-c]quinoline core found in the Martinella alkaloids was constructed through an intramolecular [3+2] azomethine ylide-alkene cy cloaddition. Some chemical manipulations of the tricycle are reported. (C) 2001 Elsevier Science Ltd. AU rights reserved.