Programmed Selective sp2 C-O Bond Activation toward Multiarylated Benzenes

被引:54
作者
Zhao, Fei [1 ,2 ]
Zhang, Yun-Fei [4 ]
Wen, Jing [5 ]
Yu, Da-Gang [1 ,2 ]
Wei, Jiang-Bo [1 ,2 ]
Xi, Zhenfeng [1 ,2 ,3 ]
Shi, Zhang-Jie [1 ,2 ,3 ]
机构
[1] Peking Univ, Coll Chem, Minist Educ, BNLMS, Beijing 100871, Peoples R China
[2] Peking Univ, Coll Chem, Minist Educ, Key Lab Bioorgan Chem & Mol Engn, Beijing 100871, Peoples R China
[3] Chinese Acad Sci, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
[4] China Agr Univ, Dept Chem, Beijing 100094, Peoples R China
[5] Lanzhou Univ, Coll Chem & Chem Engn, Lanzhou 730000, Gansu, Peoples R China
关键词
CROSS-COUPLING REACTIONS; CARBON-CARBON BONDS; SUZUKI-MIYAURA; GRIGNARD-REAGENTS; STEREOCONTROLLED SYNTHESIS; BIOLOGICAL EVALUATION; BIARYL CONSTRUCTION; EFFICIENT SYNTHESIS; SYNTHETIC METHODS; DIRECT ARYLATION;
D O I
10.1021/ol4011757
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A variety of important multiarylated benzenes were efficiently synthesized from phloroglucinol derivatives 1 through sequential cross-couplings via Pd-catalyzed C-OTs, Ni-catalyzed C-OC(O)NEt2, and C-OMe bond activation. High selectivity was achieved based on the rational design and inherent diversity in the reactivity of different C-O bonds.
引用
收藏
页码:3230 / 3233
页数:4
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