An intramolecular azomethine ylide–alkene cycloaddition approach to pyrrolo[3,2-c]quinolines-synthesis of a C2-truncated martinelline model
2001; Elsevier BV; Volume: 57; Issue: 19 Linguagem: Inglês
10.1016/s0040-4020(01)00315-5
ISSN1464-5416
AutoresHossen Mahmud, Carl J. Lovely, H. V. Rasika Dias,
Tópico(s)Chemical synthesis and alkaloids
ResumoThe hexahydropyrrolo[3,2-c]quinoline core found in the Martinella alkaloids was constructed through an intramolecular [3+2] azomethine ylide–alkene cycloaddition. Some chemical manipulations of the tricycle are reported.
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