Asymmetric Catalytic Halofunctionalization of α,β-Unsaturated Carbonyl Compounds

被引:47
|
作者
Cai, Yunfei [1 ,2 ]
Liu, Xiaohua [1 ]
Zhou, Pengfei [1 ]
Feng, Xiaoming [1 ]
机构
[1] Sichuan Univ, Coll Chem, Minist Educ, Key Lab Green Chem & Technol, Chengdu 610064, Sichuan, Peoples R China
[2] Chongqing Univ, Sch Chem & Chem Engn, 174 Shazheng St, Chongqing 400030, Peoples R China
来源
JOURNAL OF ORGANIC CHEMISTRY | 2019年 / 84卷 / 01期
基金
中国国家自然科学基金;
关键词
HIGHLY EFFICIENT SYNTHESIS; ENANTIOSELECTIVE BROMOAMINOCYCLIZATION; STEREOSELECTIVE AMINOBROMINATION; AMINOHALOGENATION REACTION; CONJUGATE ADDITION; INTERMOLECULAR HALOETHERIFICATION; SELECTIVE BROMOCYCLIZATION; NEIGHBORING GROUPS; ACID-DERIVATIVES; OLEFINS;
D O I
10.1021/acs.joc.8b01951
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Halofunctionalization methods enable the vicinal difunctionalization of alkenes with heteroatom nucleophiles and halogen moieties. As a fundamental transformation in organic synthesis, the catalytic asymmetric variants have only recently been reported. In sharp contrast to the asymmetric halocyclization of simple alkenes which involves a nucleophile-assisted alkene activation process, the asymmetric halofunctionalization of enones developed by our laboratory features an electrophile-assisted 1,4-addition pathway. Our work in this area has resulted in the development of several different types of regio-, diastereo-, and enantioselective processes, including inter- and intramolecular haloaminations, haloetherifications, and haloazidations. The scope, updated mechanism, limitations, and future perspective of these reactions are discussed.
引用
收藏
页码:1 / 13
页数:13
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