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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:
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.
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页码:1 / 13
页数:13
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