Synthesis of Novel 2,3-Dihydro-2,3-furandione and 1H-Pyrazole-3-Carboxylic Acid Derivatives
Corresponding Author(s) : Sevket Hakan Ungoren
hungoren@erciyes.edu.tr
Asian Journal of Chemistry,
Vol. 16 No. 2 (2004): Vol 16 Issue 2
Abstract
The reaction of oxalyl chloride with unsymmetrically substituted diketones (1a-e) furnished the corresponding 2,3-dihydro-2,3-furandiones (2a-e). In addition, 1H-phrazole-3-carboxylic acids (5c-e) were synthesized by the reaction of (2c-e) with phenylhydrazine and 1,5-diphenylcarbazide.
Keywords
1H-Pyrazole-3-carboxylic acid
Michael-type addition
2,3-Dihydro-2,3-furandione
Cyclocondensation
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Hakan Ungoren, S.; Deniz, B.; Altural, B. Synthesis of Novel 2,3-Dihydro-2,3-Furandione and 1H-Pyrazole-3-Carboxylic Acid Derivatives. ajc 2016, 16, 805-810.
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