Chiral Phosphoric Acid Catalyzed Asymmetric Ring Contraction of Isoxazoles under Dye-Free Photodriven Conditions
Cooperative phosphoric acid/photocatalysis enables novel asymmetric methods, and prior systems are largely confined to radicals generated from photoredox, energy-transfer, or EDA-complex mechanisms. Reported herein is excitation of chiral phosphoric acid–isoxazole adduct to deliver enantioenriched 2H-azirines via ring contraction. This catalytic system proceeds under dye-free and operationally simple conditions with high enantioselectivity and efficiency. Mechanistic studies revealed that the isoxazole undergoes CPA-assisted photoexcitation and homolysis of the N–O bond to a triplet diradical. A subsequent C–C rotation prior to the C–N cyclization has been established as the enantio-determining step.
Authors
- X.C. Li (ORCID: https://orcid.org/0000-0002-5981-2762)
- Qiao Li (ORCID: https://orcid.org/0000-0001-8294-8169)
- Xia Gao (ORCID: https://orcid.org/0009-0001-0480-1468)
- Xiaotian Qi (ORCID: https://orcid.org/0000-0001-5420-5958)
Institutions
- Ministry of Education of the People's Republic of China (CN)
- Wuhan University (CN)
- Shaanxi Normal University (CN)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2026-05-29
- DOI
- https://doi.org/10.1021/jacs.6c06340
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- Shaanxi Normal University
- National Key Research and Development Program of China