Carbon-Nitrogen bond-forming reactions of diakyl azodicarboxylate: A promsing synthetic strategy

Vijay Nair, G; Biju, A T; Smitha C. Mathew; Babu, B P

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dc.contributor.author	Vijay Nair, G
dc.contributor.author	Biju, A T
dc.contributor.author	Smitha C. Mathew
dc.contributor.author	Babu, B P
dc.date.accessioned	2016-01-18T07:03:01Z
dc.date.available	2016-01-18T07:03:01Z
dc.date.issued	2008
dc.identifier.citation	Chemistry-An Asian Journal 3(5):810-820;2008	en_US
dc.identifier.issn	1861-4728
dc.identifier.uri	http://ir.niist.res.in:8080/jspui/handle/123456789/2111
dc.description.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.	en_US
dc.language.iso	en	en_US
dc.publisher	Wiley	en_US
dc.subject	Amination reactions	en_US
dc.subject	Azodicarboxylates	en_US
dc.subject	C-N bond formation	en_US
dc.subject	Heterocycles	en_US
dc.subject	Huisgen zwitterion	en_US
dc.subject	Asymmetric alpha-amination	en_US
dc.subject	Amino-acid derivatives	en_US
dc.subject	Baylis-hillman reactions	en_US
dc.subject	Mitsunobu reaction	en_US
dc.subject	Enantioselective amination	en_US
dc.subject	Diethyl azodicarboxylate	en_US
dc.subject	Bicyclic hydrazines	en_US
dc.subject	Stereoselective amination	en_US
dc.subject	Electrophilic amination	en_US
dc.title	Carbon-Nitrogen bond-forming reactions of diakyl azodicarboxylate: A promsing synthetic strategy	en_US
dc.type	Article	en_US