Aryne [3 + 2] cycloaddition with N-sulfonylpyridinium imides and in situ generated N-sulfonylisoquinolinium imides: a potential route to pyrido[1,2-b]indazoles and indazolo[3,2-a]isoquinolines

The aryne [3 + 2] cycloaddition process with pyridinium imides breaks the aromaticity of the pyridine ring. By equipping the imide nitrogen with a sulfonyl group, the intermediate readily eliminates a sulfinate anion to restore the aromaticity, leading to the formation of pyrido[1,2-b]indazoles. The...

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Veröffentlicht in:Organic & biomolecular chemistry 2012-03, Vol.10 (9), p.1922-1930
Hauptverfasser: Zhao, Jingjing, Li, Pan, Wu, Chunrui, Chen, Hongli, Ai, Wenying, Sun, Renhong, Ren, Hailong, Larock, Richard C, Shi, Feng
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Sprache:eng
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