化学
炔烃
转移加氢
烯烃
催化作用
硅烷
区域选择性
芳基
氘
铜
有机化学
产量(工程)
光化学
组合化学
烷基
硅烷
钌
冶金
材料科学
物理
量子力学
作者
Samantha E. Sloane,Albert Reyes,Zoua Pa Vang,Lingzi Li,Kiera T. Behlow,Joseph R. Clark
出处
期刊:Organic Letters
[American Chemical Society]
日期:2020-11-10
卷期号:22 (22): 9139-9144
被引量:37
标识
DOI:10.1021/acs.orglett.0c03632
摘要
A copper-catalyzed reduction of alkynes to alkanes and deuterated alkanes is described under transfer hydrogenation and transfer deuteration conditions. Commercially available alcohols and silanes are used interchangeably with their deuterated analogues as the hydrogen or deuterium sources. Transfer deuteration of terminal and internal aryl alkynes occurs with high levels of deuterium incorporation. Alkyne-containing complex natural product analogues undergo transfer hydrogenation and transfer deuteration selectively, in high yield. Mechanistic experiments support the reaction occurring through a cis-alkene intermediate and demonstrate the possibility for a regioselective alkyne transfer hydrodeuteration reaction.
科研通智能强力驱动
Strongly Powered by AbleSci AI