Cobalt-catalyzed Synthesis of Homoallylic Amines from Imines and Terminal Alkenes

被引:7
|
作者
Tanaka, Ryo [1 ]
Kojima, Masahiro [1 ]
Yoshino, Tatsuhiko [1 ]
Matsunaga, Shigeki [1 ]
机构
[1] Hokkaido Univ, Fac Pharmaceut Sci, Kita Ku, Kita 12 Nishi 6, Sapporo, Hokkaido 0600812, Japan
关键词
Imono-ene reaction; Cobalt; Terminal alkene; CARBONYL-ENE REACTION; ALLYLIC C(SP(3))-H BOND; ORGANIC-SYNTHESIS; ORGANOMETALLIC REAGENTS; ASYMMETRIC-SYNTHESIS; ATOM ECONOMY; ALPHA-AMINO; ALLYLATION; FUNCTIONALIZATION; EFFICIENT;
D O I
10.1246/cl.190378
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Homoallylic amines are important synthetic targets in organic synthesis. Compared to other conventional allylation reactions using pre-functionalized allylic compounds, the allylation of imines using alkenes represents an attractive strategy to access homoallylic amines, especially in terms of atom- and step-economy. Here we report that a dicationic Cp*Co-III catalyst efficiently promotes the allylation reactions of aliphatic imines with simple terminal alkenes under mild reaction conditions. The allylation reactions would proceed via an imino-ene type mechanism, inwhich the Cp*Co-III catalyst works as a Lewis acid.
引用
收藏
页码:1046 / 1049
页数:4
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