Asymmetric Catalytic Friedel-Crafts Reactions of Unactivated Arenes

被引:16
|
作者
Brunen, Sebastian [1 ]
Mitschke, Benjamin [1 ]
Leutzsch, Markus [1 ]
List, Benjamin [1 ]
机构
[1] Max Planck Inst Kohlenforsch, D-45470 Mulheim An Der Ruhr, Germany
关键词
ENANTIOSELECTIVE ADDITION; AROMATIC-SUBSTITUTION; AMINO-ACIDS; ALKYLATION; DERIVATIVES; BENZENE; INDOLES; ESTERS;
D O I
10.1021/jacs.3c05148
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Since its discovery more than a century ago, the Friedel-Craftsreaction has manifested itself as a powerful method for the introductionof carbon substituents to arenes. Despite its potential generality,the scope of the reaction is intrinsically limited by the arene'snucleophilicity, which has previously restrained the applicabilityof asymmetric variants to activated substrates. To overcome this fundamentallimitation, we report herein an asymmetric Friedel-Crafts reactionof unactivated, purely hydrocarbon arenes, alkoxybenzenes, and heteroareneswith N,O-acetals to give enantioenrichedarylglycine esters. Highly regio- and stereoselective C-C bondformation was achieved using strong and confined Bronsted acidorganocatalysts, enabling the first asymmetric catalytic Friedel-Craftsreaction of simple alkylbenzenes.
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页码:15708 / 15713
页数:6
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