Palladium-Catalyzed Alkynylation of Enones with Alkynylsilanes via C-C Bond Activation

被引:7
|
作者
Liu, Yu-Wen [1 ,2 ]
Li, Ling-Jun [1 ,2 ]
Xu, Hui [1 ]
Dai, Hui-Xiong [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, CAS Key Lab Receptor Res, Shanghai 201203, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Hangzhou Inst Adv Study, Sch Pharmaceut Sci & Technol, Hangzhou 310024, Peoples R China
来源
JOURNAL OF ORGANIC CHEMISTRY | 2022年 / 87卷 / 10期
基金
中国国家自然科学基金;
关键词
H ALKYNYLATION; SONOGASHIRA REACTION; ARYL KETONES; OXIME ESTERS; 1,3-ENYNES; ALKENES; LIGAND; FUNCTIONALIZATION; CYCLIZATIONS; ACRYLAMIDES;
D O I
10.1021/acs.joc.2c00498
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
We report herein the synthesis of 1,3-enynes via palladium-catalyzed cross-coupling between enone derivatives and alkynylsilanes. The employment of an appropriate pyridine-oxazoline ligand is the key to the C-C cleavage and the high E/Z stereoselectivity. This protocol features broad substrate scope and wide functional-group tolerance, affording the desired products in moderate-to-good yields. Late-stage diversification of natural product beta-ionone further demonstrated the synthetic utility of this protocol.
引用
收藏
页码:6807 / 6811
页数:5
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