Efficient syntheses of 4-iodopyridine and of 4-pyridylboronic acid pinacol ester

Article abstract of DOI:10.1080/00397919608003763

4-Iodopyridine can be prepared in good yield by low temperature diazotation-Sandmeyer reaction of the corresponding amine, then efficiently converted to the air-stable pinacol ester of 4-pyridylboronic acid.

Full text of DOI:10.1080/00397919608003763

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Synthetic Communications: An
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Efficient Syntheses of 4-
Iodopyridine and of 4-
Pyridylboronic Acid Pinacol
Ester
C. Coudret a
a Molecular Electronics Group, CEMES, CNRS,
BP4347, 29 rue Jeanne Marvig, 31055, Toulouse
Cedex, France
Version of record first published: 21 Aug 2006
To cite this article: C. Coudret (1996): Efficient Syntheses of 4-Iodopyridine and of 4-
Pyridylboronic Acid Pinacol Ester, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 26:19, 3543-3547
To link to this article: http://dx.doi.org/10.1080/00397919608003763
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