α-C-H Functionalization of π-Bonds Using Iron Complexes: Catalytic Hydroxyalkylation of Alkynes and Alkenes

被引:40
|
作者
Wang, Yidong [1 ]
Zhu, Jin [1 ]
Durham, Austin C. [1 ]
Lindberg, Haley [1 ]
Wang, Yi-Ming [1 ]
机构
[1] Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA
关键词
ENANTIOSELECTIVE SYNTHESIS; CARBONYL PROPARGYLATION; ALLYLIC ALCOHOLS; ALDEHYDES; LIGAND; OXIDATION; CHEMISTRY; ARYLATION; REAGENTS; DEPROTONATION;
D O I
10.1021/jacs.9b11716
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The discovery of catalytic systems based on earth-abundant transition metals for the functionalization of C-H bonds enables streamlined and sustainable solutions to problems in synthetic organic chemistry. In this Communication, we disclose an iron-based catalytic system for the functionalization of propargylic and allylic C-H bonds. Inexpensive and readily available cyclopentadienyliron(II) dicarbonyl complexes were employed as catalysts for a novel deprotonative activation mode for C-H functionalization, an approach that allows for the direct union of unsaturated building blocks with aryl aldehydes and other carbonyl electrophiles to deliver a range of unsaturated alcohol coupling products under operationally simple and functional group tolerant reaction conditions.
引用
收藏
页码:19594 / 19599
页数:6
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