阿托品
轴对称性
化学
苯乙烯
催化作用
组合化学
轴手性
烯烃
不稳定性
产量(工程)
对偶(语法数字)
对映选择合成
反应条件
计算化学
立体异构
航程(航空)
氢甲酰化
有机化学
双重角色
立体化学
生物催化
作者
Ya-Sheng Cao,Yuan Hu,Wanru Guo,Botao Yu,Ya Chen,Yanjun Xie,G. B. Deng
标识
DOI:10.1021/acscatal.6c01105
摘要
The atroposelective synthesis of axially chiral styrenes remains a formidable challenge due to the configurational lability and the difficulty in controlling alkene geometry. Herein, we report a synergistic photoredox/copper-catalyzed carbocyanation of terminal alkynes that enables efficient access to these valuable scaffolds. Under redox-neutral conditions, a wide range of readily available N-hydroxyphthalimide esters and 2-aminoaryl alkynes are efficiently converted into the corresponding styrene atropisomers in good yields with high enantioselectivity and E-selectivity. The practicality of this method is highlighted by successful scale-up reactions and versatile downstream transformations, providing a general and efficient strategy for synthesizing configurationally unstable axially chiral alkenes.
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