Issue 16, 1997
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Synthesis of the marine dibromooxoindoline convolutamydine C

Soyfur Miah,   Christopher J. Moody,   Ian C. Richards  and  Alexandra M. Z. Slawin  

Abstract

A synthesis of the marine 4,6-dibromo-3-hydroxyoxoindoline convolutamydine C 3 is described. The key steps are the rhodium(II) perfluorobutyramide catalysed cyclisation of diazoamide 17 to give the oxoindoline 18, and the subsequent high yielding one-pot hydrolysis–decarboxylation–oxidation of 19 to 20. X-Ray crystal structures have been determined for the diazoamides 10 and 17 and for the oxoindolines 11 and 13.

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Article information

DOI
https://doi.org/10.1039/A700683G
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1997, 2405-2412

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Synthesis of the marine dibromooxoindoline convolutamydine C

S. Miah, C. J. Moody, I. C. Richards and A. M. Z. Slawin, J. Chem. Soc., Perkin Trans. 1, 1997, 2405 DOI: 10.1039/A700683G

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