Synthesis of Acyl Hydrazides from Carboxamides and Hydrazine Hydrate Under Metal-Free Conditions at Room Temperature
| dc.contributor.author | Singh S.; Kandasamy J. | |
| dc.date.accessioned | 2025-05-23T11:17:48Z | |
| dc.description.abstract | Synthesis of acyl hydrazides from amides has been achieved at room temperature through N-activation reactions. A wide spectrum of functionalized primary and secondary amides was initially converted into N-Boc, N-nitroso and N-tosyl amides and subjected to transamidation with hydrazine hydrate to obtain the desired acyl hydrazides in 76–94% yields. Broad substrate scope, shorter reaction time and mild reaction conditions are the merits of the developed methodology. © 2023 Wiley-VCH GmbH. | |
| dc.identifier.doi | https://doi.org/10.1002/ajoc.202300115 | |
| dc.identifier.uri | http://172.23.0.11:4000/handle/123456789/7831 | |
| dc.relation.ispartofseries | Asian Journal of Organic Chemistry | |
| dc.title | Synthesis of Acyl Hydrazides from Carboxamides and Hydrazine Hydrate Under Metal-Free Conditions at Room Temperature |