Copper-Catalyzed Formal Transfer Hydrogenation/Deuteration of Aryl Alkynes

被引:38
作者
Sloane, Samantha E. [1 ]
Reyes, Albert [1 ]
Vang, Zoua Pa [1 ]
Li, Lingzi [1 ]
Behlow, Kiera T. [1 ]
Clark, Joseph R. [1 ]
机构
[1] Marquette Univ, Dept Chem, Milwaukee, WI 53233 USA
关键词
SELECTIVE SEMIHYDROGENATION; TERMINAL ALKYNES; REDUCTION; ALKENES; DRUG; DEUTERIUM; HYDROSILANE; DEUTERATION; REACTIVITY; ETHANOL;
D O I
10.1021/acs.orglett.0c03632
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
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.
引用
收藏
页码:9139 / 9144
页数:6
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