A convenient rearrangement of 1-phenylpyrrole-2-carboxaldehydes into their 3-isomers

Article abstract of DOI:10.1080/00397919408010193

1-Phenylpyrrole-2-carboxaldehydes are selectively and in high yield converted by treatment with trifluoromethanesulfonic acid (triflic acid) to 1-phenylpyrrole-3-carboxaldehydes.

Full text of DOI:10.1080/00397919408010193

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Synthetic Communications: An
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A Convenient Rearrangement
of 1-Phenylpyrrole-2-
carboxaldehydes into Their 3-
Isomers
Patrick Dallemagne a , Sylvain Rault a , Frédéric Fabis
a , Hugues Dumoulin a & Max Robba a
a Centre d'Etudes et de Recherche sur le Médicament
de Normandie Laboratoire de Chimie Thérapeutique ,
U.F.R. des Sciences Pharmaceutiques 1 , rue
Vaubénard, 14032, Caen, France
Published online: 23 Sep 2006.
To cite this article: Patrick Dallemagne , Sylvain Rault , Frédéric Fabis , Hugues
Dumoulin & Max Robba (1994) A Convenient Rearrangement of 1-Phenylpyrrole-2-
carboxaldehydes into Their 3-Isomers, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 24:13, 1855-1857,
DOI: 10.1080/00397919408010193
To link to this article: http://dx.doi.org/10.1080/00397919408010193
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