Cu-Catalyzed Aminoacyloxylation of Unactivated Alkenes of Unsaturated Hydrazones with Manifold Carboxylic Acids toward Ester-Functionalized Pyrazolines

被引:35
|
作者
Liu, Rui-Hua [1 ]
Wang, Zi-Qing [1 ]
Wei, Bang-Yi [1 ]
Zhang, Jian-Wu [1 ]
Zhou, Bo [1 ]
Han, Bing [1 ]
机构
[1] Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Gansu, Peoples R China
基金
中国国家自然科学基金;
关键词
UREA-TETHERED ALKENES; INTRAMOLECULAR AMINOHYDROXYLATION; AQUEOUS-SOLUTION; BOND-CLEAVAGE; AMINOOXYGENATION; OLEFINS; DIAMINATION; CYCLIZATION; ASPIRIN; AMINO;
D O I
10.1021/acs.orglett.8b01507
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A copper-catalyzed aminoacyloxylation of unactivated alkenes of unsaturated hydrazones is achieved by using various commercially available carboxylic acids as the acyloxylating reagents and di-tert-butyl peroxide (DTBP) as the oxidant. By using this method, a sequence of structurally diversiform acyloxyl-substituted pyrazolines are efficiently synthesized. Significantly, many carboxyl-containing drugs and bioactive molecules with unprotected functional groups are compatible in this reaction.
引用
收藏
页码:4183 / 4186
页数:4
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