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Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/2111
Title: Carbon-Nitrogen bond-forming reactions of diakyl azodicarboxylate: A promsing synthetic strategy
Authors: Vijay Nair, G
Biju, A T
Smitha C. Mathew
Babu, B P
Keywords: Amination reactions
Azodicarboxylates
C-N bond formation
Heterocycles
Huisgen zwitterion
Asymmetric alpha-amination
Amino-acid derivatives
Baylis-hillman reactions
Mitsunobu reaction
Enantioselective amination
Diethyl azodicarboxylate
Bicyclic hydrazines
Stereoselective amination
Electrophilic amination
Issue Date: 2008
Publisher: Wiley
Citation: Chemistry-An Asian Journal 3(5):810-820;2008
Abstract: Azodicarboxylates 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.
URI: http://ir.niist.res.in:8080/jspui/handle/123456789/2111
ISSN: 1861-4728
Appears in Collections:2008

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