2005•Australian Journal of ChemistryRequires access

N,N-Dialkyl (N'-Chlorosulfonyl)chloroformamidines in Heterocyclic Synthesis. I. The Preparation of [1,2,3,5]Thiatriazole and [1,3,2,4]Oxathiadiazole Derivatives

Gary D. Fallon, Saba Jahangiri, Andris J. Liepa, Ruth C. J. Woodgate

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Abstract

N,N-Dialkyl (N'-chlorosulfonyl)chloroformamidines 1 react regiospecifically with hydrazine derivatives to give [1,2,3,5]thiatriazole dioxides. Reaction of 1 with hydroxamic acids and N-methyl hydroxylamine gave derivatives of [1,3,2,4]oxathiadiazole dioxide 7, a new heterocycle.

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N,N-Dialkyl (N'-chlorosulfonyl)chloroformamidines 1 react regiospecifically with hydrazine derivatives to give [1,2,3,5]thiatriazole dioxides. Reaction of 1 with hydroxamic acids and N-methyl hydroxylamine gave derivatives of [1,3,2,4]oxathiadiazole dioxide 7, a new heterocycle.

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Available abstract

N,N-Dialkyl (N'-chlorosulfonyl)chloroformamidines 1 react regiospecifically with hydrazine derivatives to give [1,2,3,5]thiatriazole dioxides. Reaction of 1 with hydroxamic acids and N-methyl hydroxylamine gave derivatives of [1,3,2,4]oxathiadiazole dioxide 7, a new heterocycle.

Key concepts: Chemistry, Hydroxylamine, Biocatalysis, Green chemistry, Hydrazine (antidepressant), Macromolecule, Ionic liquid, Supramolecular chemistry

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N,N-Dialkyl (N'-Chlorosulfonyl)chloroformamidines in Heterocyclic Synthesis. I. The Preparation of [1,2,3,5]Thiatriazole and [1,3,2,4]Oxathiadiazole Derivatives — Research Paper | ScholarLens