Palladium-catalyzed cascade metallo-ene/Suzuki coupling reaction of allenamides

被引:34
|
作者
Liang, Hanbing [1 ]
Yan, Fachao [1 ]
Dong, Xu [1 ]
Liu, Qing [1 ]
Wei, Xiaobing [1 ]
Liu, Sheng [2 ]
Dong, Yunhui [1 ]
Liu, Hui [1 ,2 ,3 ]
机构
[1] Shandong Univ Technol, Sch Chem Engn, 266 West Xincun Rd, Zibo 255049, Peoples R China
[2] Zibo Entry & Exit Inspect & Quarantine Bur, Tech Ctr, Zibo 255031, Peoples R China
[3] Hunan Univ, Coll Mat Sci & Engn, Changsha 410082, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
OXIDATIVE CARBOCYCLIZATION-BORYLATION; PEPTIDASE-IV INHIBITOR; C BOND FORMATION; ENE REACTIONS; ARYLATING CARBOCYCLIZATION; CARBONYLATION-ALKYNYLATION; REGIOSELECTIVE SYNTHESIS; CYCLOISOMERIZATION; CYCLIZATION; 1,6-DIENES;
D O I
10.1039/c7cc00191f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new type of cascade metallo-ene/Suzuki coupling reaction of allenamides catalyzed by palladium is described. A variety of polyfunctionalized 2,3-dihydropyrrole derivatives, which are important structural motifs for bioactive molecules, were furnished with excellent yields. Two new Csp(3)-Csp(2) bonds were constructed in one pot efficiently. The reductive elimination from p-allyl palladium complex presented excellent regioselectivity to the terminal C1 position. The unique terminal alkene was one of the most easily functionalized groups, providing these molecules with a potential transformation to much more complicated molecules.
引用
收藏
页码:3138 / 3141
页数:4
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