Copper-Catalyzed Hydrofunctionalization of Alkynes

被引:57
|
作者
Suess, Alison M. [1 ]
Lalic, Gojko [1 ]
机构
[1] Univ Washington, Dept Chem, Seattle, WA 98105 USA
关键词
catalysis; copper; metal hydrides; N-heterocyclic carbenes; electrophiles; REDUCTIVE ALDOL REACTION; CONJUGATE REDUCTION; ALLYLIC ALCOHOLS; ENANTIOSELECTIVE SYNTHESIS; TRANSFER HYDROGENATION; STRYKERS REAGENT; EFFICIENT METHOD; KETONES; HYDRIDE; ALDEHYDES;
D O I
10.1055/s-0035-1561357
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
We have developed a general approach to the catalytic hydrofunctionalization of alkynes, involving hydrocupration and electrophilic functionalization of the resulting alkenylcopper intermediate. Using this approach with different electrophiles we have developed three transformations: semireduction, hydrobromination, and hydroalkylation of alkynes. In the context of a brief history of copper hydride complexes in organic chemistry, in this account we describe the key developments that inspired and enabled our research. We also describe the reaction development, the scope, and the mechanism of these transformations. In the process, we highlight some of the challenges inherent to our approach and summarize new insights that allowed us to successfully address them. 1 Introduction 2 Semireduction 3 Hydrobromination 4 Hydroalkylation 5 Conclusions
引用
收藏
页码:1165 / 1176
页数:12
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