Condensation of 1, 2-dicarbonyl compounds with modified Huisgen zwitterions: synthesis of N-aryl–N-acyl hydrazones. Issue 3 (19th December 2019)

• Record Type: Journal Article
• Authors: Liu, Jialin; Cao, Jilei; Liu, Rongfang; Li, Ruifeng; Qiao, Yan; Zhou, Rong
• Is Part Of: Organic & biomolecular chemistry. Volume 18:Issue 3(2019)
• Page Start: 530
• Page End: 537
• Publication Date: 2019-12-19
• Subjects: Chemistry, Organic -- Periodicals; Bioorganic chemistry -- Periodicals; Chemistry, Physical organic -- Periodicals; 547
• DOI: 10.1039/c9ob02508a
• Languages: English
• ISSNs: 1477-0520

Abstract

Abstract : The reactivity patterns of the modified Huisgen zwitterions derived from arylazocarboxylates toward 1, 2-dicarbonyl compounds have been studied for the first time for a facile synthesis of N -aryl– N -acyl hydrazones. Abstract : A phosphine-mediated deoxygenative condensation of 1, 2-dicarbonyl compounds such as aroylformates, α-diketones, and isatins with arylazocarboxylates has been developed for a facile synthesis of N -aryl– N -acyl hydrazones in moderate to excellent yields under very mild conditions. Mechanistic investigation based on 31 P NMR tracking experiments unveils that the reaction is initiated with the in situ formation of the modified Huisgen zwitterions from arylazocarboxylates and PPh3 and proceeds via a nitrogen to nitrogen ester group migration process. This study also represents the first exploration of the reactivity patterns of the modified Huisgen zwitterions derived from arylazocarboxylates toward electrophiles such as 1, 2-dicarbonyl compounds.