Issue 0, 1982
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Indole β-nucleophilic substitution. Part 3. Synthesis of four isomeric pyrido[x′,y′:5,6]oxepino[3,2-b]indolones

Michael G. Beal,   William R. Ashcroft,   Melanie M. Cooper  and  John A. Joule  

Abstract

Condensations of 2-lithio-1-phenylsulphonylindole with the four pyridine analogues of phthalide gave 1-phenylsulphonylindol-2-yl o-hydroxymethylpyridyl ketones, from which on treatment with base were obtained the title compounds, by a process of intramolecular Indole β-nucleophilic substitution. This new aspect of Indole chemistry is discussed in the context of other related processes.

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Article information

DOI
https://doi.org/10.1039/P19820000435
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1982, 435-439

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Indole β-nucleophilic substitution. Part 3. Synthesis of four isomeric pyrido[x′,y′:5,6]oxepino[3,2-b]indolones

M. G. Beal, W. R. Ashcroft, M. M. Cooper and J. A. Joule, J. Chem. Soc., Perkin Trans. 1, 1982, 435 DOI: 10.1039/P19820000435

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