Abstract
Dioxazolones and phosphines have been used to access N-acyl iminophosphoranes in copper(I) catalysis under simple thermal conditions. The synthetic utility of this protocol is demonstrated by a broad range of substrates with an excellent atom-economy. The optimization process showed that copper demonstrated as catalytic amount toward the targeted transformation. Functionalization studies of N-acyl iminophosphoranes were also conducted. Our reaction protocol is compatible with an example of a bioactive motif-containing N-acyl iminophosphorane analogue.
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Park, J., Krishnapriya, A. U., Park, Y., Kim, M., Reidl, T. W., Kuniyil, R., & Son, J. (2023). Copper(I)-Catalyzed Decarboxylative N-Phosphorylation: Modular Preparation of N-Acyl Iminophosphoranes Using Dioxazolones and Phosphines. Advanced Synthesis and Catalysis, 365(24), 4495–4501. https://doi.org/10.1002/adsc.202300693
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