Double-Oxidative Dehydrogenative (DOD) [4+2]-Cyclization/Oxidative Aromatization Tandem Reaction of Glycine Derivatives with Ethylbenzenes

被引:42
作者
Jiang, Wei [1 ]
Wang, Yajun [1 ]
Niu, Pengfei [1 ]
Quan, Zhengjun [1 ]
Su, Yingpeng [1 ]
Huo, Congde [1 ]
机构
[1] Northwest Normal Univ, Coll Chem & Chem Engn, Key Lab Ecoenvironm Related Polymer Mat, Minist Educ, Lanzhou 730070, Gansu, Peoples R China
基金
中国国家自然科学基金;
关键词
C-H FUNCTIONALIZATION; BOND FUNCTIONALIZATION; COUPLING REACTION; VISIBLE-LIGHT; ESTERS; AMINES; QUINOLINE-2-CARBOXYLATES; TETRAHYDROISOQUINOLINES; CYCLIZATION; INHIBITORS;
D O I
10.1021/acs.orglett.8b01941
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The double-oxidative dehydrogenative (DOD) cyclization represents one of the most straightforward and atom-economical methods for cyclic structure formation. A Cu(II)/DDQ/O-2 system catalyzed DOD [4 + 2]-annulation/oxidative aromatization tandem reaction of readily available glycine derivatives and alkylbenzenes was established. This approach facilitates rapid access to a broad scope of substituted quinoline-2-carboxylate derivatives, an important motif in drug discovery. The reaction could feasibly be applied to a 10 gram scale synthesis.
引用
收藏
页码:4649 / 4653
页数:5
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