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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 43, 2013 - Issue 12
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Original Articles

Chemoselective and Regiospecific Formylation of 1-Phenyl-1H-pyrazoles Through the Duff Reaction

, , , , , , , , , , & show all
Pages 1633-1639 | Received 23 Nov 2011, Accepted 11 Jan 2012, Published online: 06 Mar 2013
 

Abstract

The synthesis of formylated 1-phenyl-1H-pyrazole derivatives under the Duff reaction conditions is reported. Our results indicate that 1-phenyl-1H-pyrazole systems containing electron-withdrawing and electron-donating substituents at the phenyl moiety react under the Duff reaction conditions to furnish formylated derivatives in good yields.

Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications® to view the free supplemental file.

GRAPHICAL ABSTRACT

ACKNOWLEDGMENTS

We are thankful to FAPEG CH02/2007, CAPES, CNPq, FAPEMIG, and INCT-INOFAR for grants and financial support.

Notes

a Determined by NMR and GC-MS.

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