4.5 Review

Transition Metal-Catalyzed Carboamination of Alkenes and Allenes: Recent Progress

Journal

ASIAN JOURNAL OF ORGANIC CHEMISTRY
Volume 11, Issue 1, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ajoc.202100552

Keywords

alkene; allene; carboamination; heterocycles; total synthesis

Funding

  1. Centurion University of Technology and Management, Odisha, India

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Vicinal carboamination of carbon-carbon multiple bonds is a reliable and efficient strategy for the quick preparation of valuable amine derivatives. Transition metal catalysis has been employed for the synthesis of N-bearing entities through inter- and intramolecular carboamination of alkenes and allenes. However, literature on carboamination of allenes is lacking compared to that on alkenes.
Vicinal carboamination of carbon-carbon multiple bonds is a highly reliable and efficient practical strategy for the quick preparation of valuable and diverse amine derivatives starting from simple synthons. The last decade has witnessed numerous practical methods employing transition metal carboamination approaches of alkenes and allenes for the synthesis of these N-bearing entities. Driven by the renaissance of transition metal catalysis, inter-and intramolecular carboamination of alkenes and allenes comprising concomitant C-N and C-C bond formation has been studied extensively. Interestingly, existing reviews describing developments on carboamination of alkenes are mostly reaction path specific and confined to a particular metal catalyst. Whereas, guiding congregation of literature on carboamination of allene is not documented. In this review, different conceptual approaches will be discussed and examples from the recent literature will be presented with special focus to the detailed reaction mechanism.

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