RETRACTED: Chemoselective Reactions of (E)-1,3-Dienes: Cobalt-Mediated Isomerization to (Z)-1,3-Dienes and Reactions with Ethylene (Retracted article. See vol. 140, pg. 2700, 2018)

被引:28
|
作者
Timsina, Yam N. [1 ]
Biswas, Souvagya [1 ]
RajanBabu, T. V. [1 ]
机构
[1] Ohio State Univ, Dept Chem & Biochem, Columbus, OH 43210 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
ASYMMETRIC HYDROVINYLATION; STEREOSELECTIVE SYNTHESIS; ALKENE ISOMERIZATION; METAL-CATALYSTS; 1,3-DIENES; BOND; COMPLEXES; ORGANOTITANIUM; HYDROGENATION; DIENYLATION;
D O I
10.1021/ja501979g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the asymmetric hydrovinylation (HV) of an E/Z-mixture of a prototypical 1,3-diene with (S,S)(DIOP)CoCl2 or (S,S)-(BDPP)CoCl2 catalyst in the presence of Me3Al, the (E)-isomer reacts significantly faster, leaving behind the Z-isomer intact at the end of the reaction. The presumed [LCo-H](+)-intermediate, especially when L is a large-bite angle ligand, similar to DIOP and BDPP, promote an unusual isomerization of (E/Z)-mixtures of 1,3-dienes to isomerically pure Z-isomers. A mechanism that involves an intramolecular hydride addition via an [eta(4)-(diene)(LCo-H)](+) complex, followed by pi-sigma-pi isomerization of the intermediate Co(allyl) species, is proposed for this reaction.
引用
收藏
页码:6215 / 6218
页数:4
相关论文
共 50 条