Feedstocks to Pharmacophores: Cu-Catalyzed Oxidative Arylation of Inexpensive Alkylarenes Enabling Direct Access to Diarylalkanes

被引:125
作者
Vasilopoulos, Aristidis [1 ]
Zultanski, Susan L. [1 ,2 ]
Stahl, Shannon S. [1 ]
机构
[1] Univ Wisconsin, Dept Chem, 1101 Univ Ave, Madison, WI 53706 USA
[2] Merck & Co Inc, Dept Proc Chem, Rahway, NJ 07065 USA
关键词
H BONDS; TOLUENE DERIVATIVES; CROSS-COUPLINGS; UNACTIVATED ALKANES; ALLYLIC OXIDATION; STEREOSPECIFIC FORMATION; C(SP(3))-H BONDS; CARBOXYLIC-ACIDS; ALKENES; LIGAND;
D O I
10.1021/jacs.7b03387
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A Cu-catalyzed method has been identified for selective oxidative arylation of benzylic C-H bonds with arylboronic esters. The resulting 1,1-diarylalkanes are accessed directly from inexpensive alkylarenes containing primary and secondary benzylic C-H bonds, such as toluene or ethylbenzene. All catalyst components are commercially available at low cost, and the arylboronic esters are either commercially available or easily accessible from the commercially available boronic acids. The potential utility of these methods in medicinal chemistry applications is highlighted.
引用
收藏
页码:7705 / 7708
页数:4
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