阿托品
化学
催化作用
轴对称性
镍
构造(python库)
立体化学
有机化学
物理
计算机科学
量子力学
程序设计语言
作者
Yu Chen,Liangrui Xiao,Yanjian Wan,Wenxing Liu,Jiuling Li,Yafei Guo
标识
DOI:10.1021/acs.orglett.5c02872
摘要
Here, we report an enantioselective nickel-catalyzed transannulation reaction through a denitrogenative strategy for the synthesis of new atropisomers under mild conditions. A series of axially chiral atropisomers bearing a chiral C-N bond were achieved with excellent enantioselectivities and regioselectivities. Moreover, a broad range of alkynes and 1,2,3-benzotriazinones were well tolerated by this method. The possible mechanism further reveals the role of nickel and the enantioselectivity control.
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