Issue 1, 1989
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Perkin communications. Diastereoselective alkylation of ketone enolates using a 1,3-dithiane 1-oxide auxiliary

Philip C. Bulman Page,   Alexandra M. Z. Slawin,   Donald Westwood  and  David J. Williams  

Abstract

Acyldithiane 1-oxides readily undergo deprotonation to give chelated metal enolates which react with iodomethane to give alkylated products with good selectivity.

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Article information

DOI
https://doi.org/10.1039/P19890000185
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1989, 185-187

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Perkin communications. Diastereoselective alkylation of ketone enolates using a 1,3-dithiane 1-oxide auxiliary

P. C. B. Page, A. M. Z. Slawin, D. Westwood and D. J. Williams, J. Chem. Soc., Perkin Trans. 1, 1989, 185 DOI: 10.1039/P19890000185

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