The AlCl3 catalyzed benzoylation of ethyl pyrrole-2-acetate: An unusual 6-substitution

Article abstract of DOI:10.1080/00397919208019277

In this study, synthetic methodologies have been developed which are potentially useful in preparing 4- and 5-aroylpyrrole-2-acetic acids bearing no alkyl substituents on the heterocyclic nitrogen. These compounds are structurally related to a class of NS

Full text of DOI:10.1080/00397919208019277

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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The AlCL3 Catalyzed
Benzoylation of Ethyl
Pyrrole-2-Acetate: An Unusual
6-Substitution
Elena Alexandrou a , Eleni Rekka a & Vassilis J.
Demopoulos a
a Department of Pharmaceutical Chemistry,
School of Pharmacy , University of Thessaloniki ,
Thessaloniki, 540 06, Greece
Published online: 23 Sep 2006.
To cite this article: Elena Alexandrou , Eleni Rekka & Vassilis J. Demopoulos
(1992) The AlCL3 Catalyzed Benzoylation of Ethyl Pyrrole-2-Acetate: An
Unusual 6-Substitution, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 22:5, 761-766, DOI:
10.1080/00397919208019277
To link to this article: http://dx.doi.org/10.1080/00397919208019277
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