Catalytic Asymmetric 1,3-Dipolar Cycloaddition/Hydroamination Sequence: Expeditious Access to Enantioenriched Pyrroloisoquinoline Derivatives
收藏NIAID Data Ecosystem2026-03-10 收录
下载链接：
https://figshare.com/articles/dataset/Catalytic_Asymmetric_1_3-Dipolar_Cycloaddition_Hydroamination_Sequence_Expeditious_Access_to_Enantioenriched_Pyrroloisoquinoline_Derivatives/5454382
下载链接
链接失效反馈官方服务：
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
