摘要
A bstract A practical and N-selective allylation of sulfenamides using Morita-Baylis-Hillman carbonates under Lewis base catalysis is reported. It features broad substrate scope, high chemoselectivity, and tolerance to various functional groups, affording diverse N-allylated sulfenamides in good to excellent yields. Gram-scale experiments confirm its scalability, facilitating the synthesis of bioactive molecules and expanding the utility of sulfenamide chemistry.
危险品化学品经营许可证(带存储)