Abstract
This review focuses on the use of dialkyl azodicarboxylates in the formation of C-N bonds through catalyzed α-amination reactions. Both metal catalyzed and organocatalyzed approaches are covered in the present report.
Keywords: Azodicarboxylates, amination, Michael reaction, transition metal, organocatalysis, Ruthenium, Iridium and Rhodium, Silver and Gold, Lanthanides, Proline Derivatives, Cinchona Alkaloids
Current Organic Chemistry
Title: Azodicarboxylates as Electrophilic Aminating Reagents
Volume: 15 Issue: 10
Author(s): Adelina Vallribera, Rosa Maria Sebastian and Alexandr Shafir
Affiliation:
Keywords: Azodicarboxylates, amination, Michael reaction, transition metal, organocatalysis, Ruthenium, Iridium and Rhodium, Silver and Gold, Lanthanides, Proline Derivatives, Cinchona Alkaloids
Abstract: This review focuses on the use of dialkyl azodicarboxylates in the formation of C-N bonds through catalyzed α-amination reactions. Both metal catalyzed and organocatalyzed approaches are covered in the present report.
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Cite this article as:
Vallribera Adelina, Maria Sebastian Rosa and Shafir Alexandr, Azodicarboxylates as Electrophilic Aminating Reagents, Current Organic Chemistry 2011; 15 (10) . https://dx.doi.org/10.2174/138527211795378083
DOI https://dx.doi.org/10.2174/138527211795378083 |
Print ISSN 1385-2728 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5348 |
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