铱
烯丙基重排
分子间力
催化作用
替代(逻辑)
级联
金鸡纳
化学
组合化学
对映选择合成
有机化学
立体化学
分子
计算机科学
色谱法
程序设计语言
作者
Yang‐Zi Liu,Chao Zheng,Shu‐Li You
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2024-10-09
卷期号:14 (20): 15743-15750
被引量:1
标识
DOI:10.1021/acscatal.4c05266
摘要
Medium-sized rings are important structural units in organic molecules of significant interest. However, their efficient synthesis, especially in a highly enantioselective manner, has been a formidable challenge. Herein, we report an enantioselective synthesis of medium-sized aza-rings by a Z-retentive asymmetric allylic substitution-enabled intermolecular cascade cyclization via iridium/cinchona dual catalysis. The reaction was performed under mild conditions and with good functional group tolerance. Various nine- to eleven-membered aza-rings can be afforded in moderate to high yields (up to 98%) and enantioselectivities (up to 93% ee). The utilization of both Z-linear allylic dipole precursor and iridium/cinchona binary catalyst is critical for the desired reactivity.
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