Copper-Catalyzed Oxidative α-Double Bond Construction in α-Amino Carbonyl Compounds via Homocoupling with Arylamine Release
Herein, we present a copper-catalyzed method for oxidative α-double bond formation in α-amino ketone compounds using DTBP as the oxidant. This process, involving homocoupling of α-amino radicals and arylamine release, efficiently produces a series of enaminone skeletons. The strategy has a broad substrate scope and functional group tolerance. In particular, arylamines bearing electron-rich substituents exhibit a pronounced reactivity. This approach facilitates the synthesis of diverse enaminones, enabling the efficient construction of nitrogen-containing heterocycles.
Authors
- Yiting Zhu (ORCID: https://orcid.org/0000-0003-1113-7507)
- Huan Wang (ORCID: https://orcid.org/0000-0002-4057-1145)
- Ming Chen (ORCID: https://orcid.org/0000-0003-4957-2934)
- Yan Jiang (ORCID: https://orcid.org/0000-0002-0748-0970)
- Yibin Wang (ORCID: https://orcid.org/0009-0005-0436-9432)
- Sen Yang (ORCID: https://orcid.org/0000-0003-3481-462X)
- Yan-fang Zhan
Institutions
- Changzhou University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2024-09-17
- DOI
- https://doi.org/10.1021/acs.orglett.4c03044
- Citations
- 3
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.75
Funders
- National Natural Science Foundation of China
- Government of Jiangsu Province
- Changzhou University