Intramolecular 1,3-Dipolar Cycloaddition of Azomethine Ylides Leading to Pyrido[2,3-b]quinolines
A convenient six-step route to the previously unknown 1H-pyrrolo[2,3-f]benzo[b][1,8]naphthyridine ring system using an intramolecular 1,3-dipolar cycloaddition of nonstabilized azomethine ylides has been described.
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Published in | Synthetic communications Vol. 39; no. 13; pp. 2258 - 2270 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
PHILADELPHIA
Taylor & Francis Group
09.06.2009
Taylor & Francis |
Subjects | |
Online Access | Get full text |
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