Synthesis of β-Isoxazole Carbonyl Derivatives and Their Analogues via Palladium-Catalyzed Sequential C(sp2)-O/C(sp2)-C(sp3) Bond Formations

被引:15
作者
Wu, Wanqing [1 ,2 ]
Li, Can [2 ]
Zhou, Fei [2 ]
Li, Jianxiao [2 ]
Xu, Xiaoqing [2 ]
Jiang, Huanfeng [2 ]
机构
[1] South China Univ Technol, State Key Lab Luminescent Mat & Devices, Guangzhou 510640, Guangdong, Peoples R China
[2] South China Univ Technol, Key Lab Funct Mol Engn Guangdong Prov, Sch Chem & Chem Engn, Guangzhou 510640, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Palladium-catalyzed; beta-Aryl aldehydes; ketones; Allylic alcohols; Isoxazoles; TANDEM INTRAMOLECULAR AMINOPALLADATION; OXIDATIVE KINETIC RESOLUTION; ALLYLIC ALCOHOLS; HECK REACTION; MOLECULAR-OXYGEN; CONJUGATE ADDITION; ARYL KETONES; C-C; ALKYLATION; STRATEGY;
D O I
10.1002/adsc.201900391
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
An efficient Pd(II)-catalyzed one-pot tandem cyclization/alkylation reaction of internal alkynes has been reported. In this reaction, a wide range of structurally diverse beta/beta-isoxazole aldehydes/ketones could be obtained in good to excellent yields from various alkynyl oxime ethers and allylic or homoallylic alcohols. The gram-scale experiment and various transformations of the newly obtained products demonstrated that this method should be a general and useful synthetic tool.
引用
收藏
页码:3813 / 3823
页数:11
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