Chiral Rhodium(III) Complex-Catalyzed Cascade Michael-Alkylation Reactions: Enantioselective Synthesis of Cyclopropanes

被引:55
|
作者
Sun, Gui-Jun [1 ]
Gong, Jun [1 ]
Kang, Qang [1 ]
机构
[1] Chinese Acad Sci, Fujian Inst Res Struct Matter, Key Lab Coal Ethylene Glycol & Its Related Techno, 155 Yangqiao Rd West, Fuzhou 350002, Peoples R China
来源
JOURNAL OF ORGANIC CHEMISTRY | 2017年 / 82卷 / 01期
关键词
CONTAINING NATURAL-PRODUCTS; ASYMMETRIC CYCLOPROPANATION; CONJUGATE ADDITION; LEWIS-ACID; ORGANOCATALYTIC CYCLOPROPANATION; VISIBLE-LIGHT; SULFUR YLIDES; DERIVATIVES; ACCEPTORS; NITROCYCLOPROPANES;
D O I
10.1021/acs.joc.6b02583
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Chiral Rh(III) complex catalyzed highly efficient enantioselective cyclopropanation of alpha,beta-unsaturated 2-aryl imidazoles or pyridine with 2-bromomalonate is developed to generate corresponding multisubstituted cyclopropanes in 70-99% yields with 93 -> 99% enantioselectivity. The proficiency of the process is also demonstrated in gram scale reaction maintaining same reactivity and selectivity level in lower catalyst loading. Moreover, the developed methodology is applicable in challenging synthesis of biscyclopropane scaffold with 97% ee in a single operation.
引用
收藏
页码:796 / 803
页数:8
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