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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.

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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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