Cobalt-catalyzed Synthesis of Homoallylic Amines from Imines and Terminal Alkenes
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作者:
Tanaka, Ryo
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Hokkaido Univ, Fac Pharmaceut Sci, Kita Ku, Kita 12 Nishi 6, Sapporo, Hokkaido 0600812, JapanHokkaido Univ, Fac Pharmaceut Sci, Kita Ku, Kita 12 Nishi 6, Sapporo, Hokkaido 0600812, Japan
Tanaka, Ryo
[1
]
Kojima, Masahiro
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Hokkaido Univ, Fac Pharmaceut Sci, Kita Ku, Kita 12 Nishi 6, Sapporo, Hokkaido 0600812, JapanHokkaido Univ, Fac Pharmaceut Sci, Kita Ku, Kita 12 Nishi 6, Sapporo, Hokkaido 0600812, Japan
Kojima, Masahiro
[1
]
Yoshino, Tatsuhiko
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Hokkaido Univ, Fac Pharmaceut Sci, Kita Ku, Kita 12 Nishi 6, Sapporo, Hokkaido 0600812, JapanHokkaido Univ, Fac Pharmaceut Sci, Kita Ku, Kita 12 Nishi 6, Sapporo, Hokkaido 0600812, Japan
Yoshino, Tatsuhiko
[1
]
Matsunaga, Shigeki
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Hokkaido Univ, Fac Pharmaceut Sci, Kita Ku, Kita 12 Nishi 6, Sapporo, Hokkaido 0600812, JapanHokkaido Univ, Fac Pharmaceut Sci, Kita Ku, Kita 12 Nishi 6, Sapporo, Hokkaido 0600812, Japan
Matsunaga, Shigeki
[1
]
机构:
[1] Hokkaido Univ, Fac Pharmaceut Sci, Kita Ku, Kita 12 Nishi 6, Sapporo, Hokkaido 0600812, Japan
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.