Journal
ORGANIC CHEMISTRY FRONTIERS
Volume 9, Issue 16, Pages 4328-4333Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2qo00741j
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Funding
- National Natural Science Foundation of China [21871053]
- Leading Innovative and Entrepreneur Team Introduction Program of Zhejiang [2019R01005]
- Open Research Fund of School of Chemistry and Chemical Engineering, Henan Normal University [2020ZD04]
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This study presents a direct approach for the synthesis of a diverse collection of valuable gamma-amino acids, as well as a variety of gamma-lactam derivatives, from readily available substrates. The transformation features mild reaction conditions, operational simplicity, and excellent functional group tolerance.
Primary gamma-amino acids are essential structural scaffolds with biological activity in pharmaceutical compounds. However, their preparation from readily available substrates remains challenging. Here, we report a direct approach to achieve the energy transfer-driven carboimination of alkenes for the synthesis of a diverse collection of valuable gamma-amino acids. Additionally, a variety of gamma-lactam derivatives are produced in only two steps from the simple substrates. Furthermore, this transformation features mild reaction conditions, operational simplicity, and excellent functional group tolerance.
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