Issue 17, 1997
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Synthesis of 1,2-fused indoles by radical cyclisation1

Christopher J. Moody  and  Claire L. Norton  

Abstract

Treatment of the 1-(ω-iodoalkyl)indole-3-carbaldehydes 8–13 with tributyltin hydride and AIBN results in radical cyclisation to give the 1,2-fused indoles 14–19 containing five-, six- and seven-membered rings. The tetrahydropyridoindole 18 is converted into the indolequinone 23.

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Article information

DOI
https://doi.org/10.1039/A700985B
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1997, 2639-2644

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Synthesis of 1,2-fused indoles by radical cyclisation1

C. J. Moody and C. L. Norton, J. Chem. Soc., Perkin Trans. 1, 1997, 2639 DOI: 10.1039/A700985B

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