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Synthesis of Acyl Hydrazides from Carboxamides and Hydrazine Hydrate Under Metal-Free Conditions at Room Temperature

dc.contributor.authorSingh S.; Kandasamy J.
dc.date.accessioned2025-05-23T11:17:48Z
dc.description.abstractSynthesis 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.doihttps://doi.org/10.1002/ajoc.202300115
dc.identifier.urihttp://172.23.0.11:4000/handle/123456789/7831
dc.relation.ispartofseriesAsian Journal of Organic Chemistry
dc.titleSynthesis of Acyl Hydrazides from Carboxamides and Hydrazine Hydrate Under Metal-Free Conditions at Room Temperature

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