In Situ-Generated Niobium-Catalyzed Synthesis of 3-Pyrroline Derivatives via Ring-Closing Metathesis Reactions

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Abstract

An active in situ-generated Nb complex was used as a catalyst in the ring-closing metathesis reaction of N,N-diallyl-p-toluenesulfonamide to afford the corresponding 3-pyrroline derivative. The Nb complex was formed from NbCl5, trimethylsilyl chloride, Zn, and PhCHCl2 in tetrahydrofuran. The Nb complex displayed high catalytic activity toward ring-closing metathesis reactions.

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Fuji, M., Chiwata, J., Ozaki, M., Aratani, S., & Obora, Y. (2018). In Situ-Generated Niobium-Catalyzed Synthesis of 3-Pyrroline Derivatives via Ring-Closing Metathesis Reactions. ACS Omega, 3(8), 8865–8873. https://doi.org/10.1021/acsomega.8b01642

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