A fluorobenzene adduct of Ti(IV), and catalytic carboamination to prepare α,β-unsaturated imines and triaryl-substituted quinolines

被引:108
作者
Basuli, F
Aneetha, H
Huffman, JC
Mindiola, DJ [1 ]
机构
[1] Indiana Univ, Dept Chem, Bloomington, IN 47405 USA
[2] Indiana Univ, Ctr Mol Struct, Bloomington, IN 47405 USA
关键词
D O I
10.1021/ja0566026
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A rare fluorobenzene adduct of group 4, [(nacnac)Ti=NAr(FC6H5)][B(C6F5)4] (nacnac- = [ArNC(tBu)]2CH, Ar = 2,6-iPr2C6H3), has been isolated and structurally characterized. This highly electron-deficient system engages readily in imine metathesis and catalyzes carboamination reactions involving diphenylacetylene and aldimines to afford α,β-unsaturated imines as well as triaryl-substituted quinolines. The latter product results from cyclization of the corresponding electron-rich α,β-unsaturated imine. Copyright © 2005 American Chemical Society.
引用
收藏
页码:17992 / 17993
页数:2
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