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Diastereoselective Cyclization of 1,5-Dienes with the C−H Bond of Pyridine Catalyzed by a Cationic Mono(phosphinoamide) Alkyl Scandium Complex
ChemCatChem ( IF 4.5 ) Pub Date : 2017-11-08 09:09:09 , DOI: 10.1002/cctc.201700980
Yanhui Chen 1 , Di Song 1 , Jing Li 2 , Xiaoyan Hu 1 , Xianjia Bi 1 , Tao Jiang 1 , Zhaomin Hou 3
Affiliation  

It rings true: The combination of a novel mono(phosphinoamido)-ligated scandium complex such as 2 a-Sc with a boron compound such as B(C6F5)3 results in a unique and highly efficient catalyst for the cis-selective cyclization of 1,5-dienes with the ortho-C(sp2)−H bond of pyridines. The resulting pyridyl-functionalized 1,3-disubstituted cyclopentane derivatives are obtained in excellent yields with high diastereoselectivities.

中文翻译:

阳离子单(膦酰胺)烷基Scan配合物催化的吡啶具有CH键的1,5-二烯的非对映选择性环化

确实如此:新型单(膦酰胺基)连接的scan络合物(如2 a -Sc)与硼化合物(如B(C 6 F 53)的结合产生了一种独特且高效的顺式选择性催化剂1,5-二烯与吡啶的邻位-C(sp 2)-H键环合。所得吡啶基官能化的1,3-二取代的环戊烷衍生物以优异的收率获得,具有高非对映选择性。
更新日期:2017-11-08
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