Z:E Selective Preparation of Disubstituted Internal Alkenes and Trisubstituted Alkenes

被引:2
|
作者
Guo Ping [1 ]
Zhou Yong [1 ]
Zhao Jie [1 ]
机构
[1] East China Univ Sci & Technol, Sch Chem & Mol Engn, Shanghai 200237, Peoples R China
关键词
disubstituted internal olefins; trisubstituted olefins; Z:E selectivity; SINGLE-ATOM CATALYSTS; STEREOSELECTIVE-SYNTHESIS; RUTHENIUM CATALYSTS; METATHESIS; PALLADIUM; HYDROGENATION; ALKYNES; ISOMERIZATION; SEMIHYDROGENATION; ACETYLENE;
D O I
10.6023/cjoc202212039
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Olefin is one of the most important bulk chemicals in industry as well as commonly used starting materials in pharmaceutical field. Since Z-olefins and E-olefins exhibit great differences in physicochemical properties and biological activities, the Z:E configuration control has been playing important roles in olefin preparation. The selective synthetic methods of Z:E configurations of disubstituted inner alkenes and trisubstituted alkenes are reviewed, including the Wittig reaction, substituted alkane elimination reaction, olefin isomerization reaction, olefin metathesis, olefin coupling reaction, and alkyne addition reaction. The catalyst types and controlling factors of Z:E selectivity in these synthetic examples are described in detail.
引用
收藏
页码:855 / 872
页数:18
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