Catalytic Asymmetric 1,3-Dipolar Cycloaddition/Hydroamination Sequence: Expeditious Access to Enantioenriched Pyrroloisoquinoline Derivatives
收藏Figshare2017-09-28 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Catalytic_Asymmetric_1_3-Dipolar_Cycloaddition_Hydroamination_Sequence_Expeditious_Access_to_Enantioenriched_Pyrroloisoquinoline_Derivatives/5454382
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资源简介：
A three-step reaction sequence has been developed to prepare a variety of enantioenriched pyrroloisoquinoline derivatives. The process involves a catalytic asymmetric azomethine ylide 1,3-dipolar cycloaddition followed by an intramolecular AuI-catalyzed alkyne hydroamination and enamine reduction.
创建时间：
2017-09-28
