Nair, Vijay ; Biju, A. T. ; Mathew, Smitha C. ; Babu, Beneesh Pattoorpadi (2008) Carbon-nitrogen bond-forming reactions of dialkyl azodicarboxylate: a promising synthetic strategy Chemistry - An Asian Journal, 3 (5). pp. 810-820. ISSN 1861-4728
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Official URL: http://onlinelibrary.wiley.com/doi/10.1002/asia.20...
Related URL: http://dx.doi.org/10.1002/asia.200700341
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.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Wiley-VCH Verlag Berlin. |
| Keywords: | Amination Reactions; Azodicarboxylates; C-N Bond Formation; Heterocycles; Huisgen Zwitterion |
| ID Code: | 84074 |
| Deposited On: | 24 Feb 2012 06:21 |
| Last Modified: | 24 Feb 2012 06:21 |
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