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dc.contributor.authorVijay Nair, G-
dc.contributor.authorBiju, A T-
dc.contributor.authorSmitha C. Mathew-
dc.contributor.authorBabu, B P-
dc.date.accessioned2016-01-18T07:03:01Z-
dc.date.available2016-01-18T07:03:01Z-
dc.date.issued2008-
dc.identifier.citationChemistry-An Asian Journal 3(5):810-820;2008en_US
dc.identifier.issn1861-4728-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/2111-
dc.description.abstractAzodicarboxylates have found applications in electrophilic amination reactions and in pericyclic reactions. The nucleophilic trigger in Mitsunobu reactions, that is, the zwitterion formed from triphenylphosphine and dialkyl azodicarboxylate, has been utilized recently in various heterocyclic constructions. This Focus Review summarizes the potential utility of azodicarboxylates in various carbon-nitrogen bond-forming reactions.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectAmination reactionsen_US
dc.subjectAzodicarboxylatesen_US
dc.subjectC-N bond formationen_US
dc.subjectHeterocyclesen_US
dc.subjectHuisgen zwitterionen_US
dc.subjectAsymmetric alpha-aminationen_US
dc.subjectAmino-acid derivativesen_US
dc.subjectBaylis-hillman reactionsen_US
dc.subjectMitsunobu reactionen_US
dc.subjectEnantioselective aminationen_US
dc.subjectDiethyl azodicarboxylateen_US
dc.subjectBicyclic hydrazinesen_US
dc.subjectStereoselective aminationen_US
dc.subjectElectrophilic aminationen_US
dc.titleCarbon-Nitrogen bond-forming reactions of diakyl azodicarboxylate: A promsing synthetic strategyen_US
dc.typeArticleen_US
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