Palladium-Catalyzed (4 + 1) Cycloaddition of Amido-Tethered Allylic Carbonates with Sulfur Ylides: Synthesis of γ-Lactam Derivatives
In this paper, we reported a palladium-catalyzed formal (4 + 1) cycloaddition reaction between amido-tethered allylic carbonates and sulfur ylides. The reaction worked well to provide γ-lactam compounds in satisfactory yields and displayed good compatibility to a wide range of functional groups. The synthetic value of the reaction was demonstrated through scale-up reaction and further transformation. A plausible reaction mechanism was also proposed.
Authors
- Yi Tang (ORCID: https://orcid.org/0000-0002-4882-5234)
- Lan Wang (ORCID: https://orcid.org/0000-0002-8931-7201)
- Mengxi Lu
- Hongchao Guo (ORCID: https://orcid.org/0000-0002-7356-4283)
- Xiao-Jing Sun (ORCID: https://orcid.org/0000-0003-2045-7350)
Institutions
- China Agricultural University (CN)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2025-08-11
- DOI
- https://doi.org/10.1021/acs.joc.5c01050
- Citations
- 1
- Primary Topic
- Cyclopropane Reaction Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.94
Funders
- National Natural Science Foundation of China