Microwave-assisted synthesis of phenylpyrimidine derivatives via Suzuki-Miyaura reactions in water
An efficient method was developed to prepare biphenylpyrimidine scaffolds via a Suzuki-Miyaura coupling reaction. In this procedure, the products were synthesized under microwave irradiation in water and analogues of biguanidine were employed as ligands.
Le, Yi,Zhang, Yan,Wang, Qin,Rao, Nian,Li, Dan,Liu, Li,Ouyang, Guiping,Yan, Longjia
supporting information
(2021/02/21)
Ruthenium-catalyzed double-fold C-H tertiary alkoxycarbonylation of arenes using di-tert-butyl dicarbonate
An efficient ruthenium-catalyzed double-fold C-H alkoxycarbonylation of arenes was developed using di-tert-butyl dicarbonate as the tertiary esterification reagent, which leads to a direct route to valuable 2,6-dicarboxylated products. This journal is
Hong, Xiaohu,Wang, Hao,Liu, Bingxin,Xu, Bin
supporting information
p. 14129 - 14132
(2014/12/11)
Palladium-Catalyzed Regioselective C-H Bond ortho-Acetoxylation of Arylpyrimidines
An efficient and regioselective palladium-catalyzed ortho C-H acetoxylation reaction was developed to afford, ortho monoacetoxylated arylpyrimidmes in good to excellent yields by using cupric trifluoroacetate as a cocatalyst. A wide variety of oxygenated
Zheng, Xiaojian,Song, Bingrui,Xu, Bin
supporting information; experimental part
p. 4376 - 4380
(2010/10/04)
Cobalt-catalyzed cross-coupling between in situ prepared arylzinc halides and 2-chloropyrimidine or 2-chloropyrazine
A cobalt-catalyzed cross-coupling of aryl halides with 2-chloropyrimidines or 2-chloropyrazines is reported in satisfactory to high yields. The key step of this procedure is the formation of aromatic organozinc reagents and their coupling with 2-chlorodia
Begouin, Jeanne-Marie,Gosmini, Corinne
supporting information; experimental part
p. 3221 - 3224
(2009/09/26)
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