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
Hakan Ungoren, S., Deniz, B., & Altural, B. (2016). Synthesis of Novel 2,3-Dihydro-2,3-furandione and 1H-Pyrazole-3-Carboxylic Acid Derivatives. Asian Journal of Chemistry, 16(2), 805–810. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/14582
Download Citation
Endnote/Zotero/Mendeley (RIS)BibTeX