Regiospecific carboalkoxylation of 2,5-dibromopyridine

Article abstract of DOI:10.1080/00397919708006053

Carboalkoxylation of 2,5-dibromopyridine with carbon monoxide and an alcohol in the presence of palladium acetate and 1,1'-bis(diphenylphosphino)ferrocene (dppf) occurs regiospecifically to afford esters of 5-bromo-pyridine-2-carboxylic acid in good yield.

Full text of DOI:10.1080/00397919708006053

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Synthetic Communications:
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Synthetic Organic Chemistry
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Regiospecific
Carboalkoxylation of 2,5-
Dibromopyridine
R. J. Chambers a & A. Marfat a
a Pfizer Central Research , Groton, CT, 06340
Published online: 22 Aug 2006.
To cite this article: R. J. Chambers & A. Marfat (1997) Regiospecific
Carboalkoxylation of 2,5-Dibromopyridine, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry,
27:3, 515-520, DOI: 10.1080/00397919708006053
To link to this article: http://dx.doi.org/10.1080/00397919708006053
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