Carbon-nitrogen bond-forming reactions of dialkyl azodicarboxylate: a promising synthetic strategy
Title | Carbon-nitrogen bond-forming reactions of dialkyl azodicarboxylate: a promising synthetic strategy |
Publication Type | Journal Article |
Year of Publication | 2008 |
Authors | Nair, V, Biju, AT, Mathew, SC, Pattoorpadi, BBabu |
Journal | Chemistry an Asian Journal |
Volume | 3 |
Issue | 5 |
Pagination | 810–820 |
Date Published | MAY |
Type of Article | Article |
Keywords | amination reactions; azodicarboxylates; C[BOND]N bond formation; heterocycles; Huisgen zwitterion |
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. |
DOI | 10.1002/asia.200700341 |
Funding Agency | Council of Scientific & Industrial Research (CSIR) - India |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 4.14 |
Divison category:
Organic Chemistry