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dc.contributor.authorNandi, G C-
dc.contributor.authorIrfana, Jesin-
dc.date.accessioned2018-07-06T10:30:39Z-
dc.date.available2018-07-06T10:30:39Z-
dc.date.issued2018-05-15-
dc.identifier.citationAdvanced Synthesis and Catalysis, 360:2465–2469en_US
dc.identifier.urihttp://10.10.100.66:8080/xmlui/handle/123456789/3163-
dc.description.abstractHerein, we describe the preparation of sulfonimidoyl azides, and demonstrate their utility in the construction of N-acyl sulfonimidamides and Nsulfonimidoyl amidines. N-Acyl sulfonimidamides were synthesized in good to very good yields via “on water” copper-catalyzed three-component coupling between sulfonimidoyl azide, alkynes and water. The use of amines as nucleophiles yielded a wide range of N-sulfonimidoyl amidines. Both reactions were completed in very short time at room temperature under mild conditions, thus establishing the potential of sulfonimidoyl azides, the aza-analogues of sulfonyl azides, as an excellent precursor to derive functionalized sulfonimidamides in one step.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectSulfonimidoyl azideen_US
dc.subjectN-Acyl sulfonimidamidesen_US
dc.subjectAmidinesen_US
dc.subjectCopper-catalyzed azide-alkyne cycloadditionen_US
dc.subjectMulticomponent reactionsen_US
dc.titleDirect Synthesis of N-Acyl Sulfonimidamides and NSulfonimidoyl Amidines from Sulfonimidoyl Azidesen_US
dc.typeArticleen_US
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