废止
化学
接受者
配体(生物化学)
催化作用
三氟甲磺酸
对映选择合成
组合化学
轴手性
立体化学
有机化学
物理
凝聚态物理
生物化学
受体
作者
Liangliang Yang,Jieyin He,Haiyang Wang,Wendi Xu,Xue Zhang,Ming Lang,Jian Wang,Shiyong Peng
标识
DOI:10.1021/acscatal.3c01219
摘要
Saturated 1,4-diazocanes are highly important for medicinal chemistry and drug discovery, but their syntheses are often tedious. Herein, we report a copper-catalyzed (5 + 3) annulation of donor–acceptor cyclopropanes with imidazolidines, thereby providing a straightforward method to access a library of saturated 1,4-diazocanes in moderate to excellent yields under mild reaction conditions. More importantly, the asymmetric version of this (5 + 3) annulation leading to optically active saturated 1,4-diazocanes is achieved by two strategies: (i) chirality transfer and (ii) dynamic kinetic asymmetric transformation by employing copper triflate with an SaBOX ligand. In addition, the analogous (6 + 3) annulation of donor–acceptor cyclopropanes with hexahydropyrimidines is also realized.
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