Organocatalytic Asymmetric Mannich/Aza-Michael Cascade Reaction of δ‑Formyl-α,β-unsaturated Ketones with Cyclic N‑Sulfimines: Enantioselective Synthesis of Benzosulfamidate-Fused Pyrrolidines
收藏Figshare2017-07-25 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Organocatalytic_Asymmetric_Mannich_Aza-Michael_Cascade_Reaction_of_Formyl-_-unsaturated_Ketones_with_Cyclic_i_N_i_Sulfimines_Enantioselective_Synthesis_of_Benzosulfamidate-Fused_Pyrrolidines/5244595
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A catalytic highly enantioselective Mannich/aza-Michael cascade reaction of δ-formyl-α,β-unsaturated ketones with cyclic N-sulfimines, promoted by diphenylprolinol TMS ether as an organocatalyst, has been developed for the synthesis of chiral benzosulfamidate-fused pyrrolidines, which generated in good yields and with high diastero- and enantioselectivities. Further chemical transformations have been performed with chiral benzosulfamidate-fused pyrrolidines
创建时间:
2017-07-25



