Palladium-Catalyzed Synthesis of Amino β-Lactones Using Aryl Amines and Alkenyl Carboxylic Acids
A palladium-catalyzed construction of amino β-lactone derivatives is described herein. This method applies readily available aryl amines and alkenyl carboxylic acids as starting materials, providing the amino β-lactone under mild reaction conditions in one step. The deuterium labeling experiment revealed that the β-H elimination process after aminopalladation was effectively suppressed under the excess amount of I<sup>-</sup>, thus enabling further oxidation and reductive elimination to afford the target amino β-lactones.
Authors
- Wanqing Wu (ORCID: https://orcid.org/0000-0001-5151-7788)
- Xiaoya Zhuo
- Huanfeng Jiang (ORCID: https://orcid.org/0000-0002-4355-0294)
- Xiangwen Tan
Institutions
- Key Laboratory of Guangdong Province (CN)
- South China University of Technology (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2025-09-03
- DOI
- https://doi.org/10.1021/acs.orglett.5c02889
- Citations
- 1
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.94
Funders
- National Natural Science Foundation of China
- Special Project for Research and Development in Key areas of Guangdong Province