Enantioselective Henry reaction catalyzed by salen-cobalt complexes
被引:118
作者:
Kogami, Y
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机构:
Keio Univ, Fac Sci & Technol, Dept Chem, Kohoku Ku, Yokohama, Kanagawa 2238522, JapanKeio Univ, Fac Sci & Technol, Dept Chem, Kohoku Ku, Yokohama, Kanagawa 2238522, Japan
Kogami, Y
[1
]
Nakajima, T
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机构:
Keio Univ, Fac Sci & Technol, Dept Chem, Kohoku Ku, Yokohama, Kanagawa 2238522, JapanKeio Univ, Fac Sci & Technol, Dept Chem, Kohoku Ku, Yokohama, Kanagawa 2238522, Japan
Nakajima, T
[1
]
Ikeno, T
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机构:
Keio Univ, Fac Sci & Technol, Dept Chem, Kohoku Ku, Yokohama, Kanagawa 2238522, JapanKeio Univ, Fac Sci & Technol, Dept Chem, Kohoku Ku, Yokohama, Kanagawa 2238522, Japan
Ikeno, T
[1
]
Yamada, T
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机构:
Keio Univ, Fac Sci & Technol, Dept Chem, Kohoku Ku, Yokohama, Kanagawa 2238522, JapanKeio Univ, Fac Sci & Technol, Dept Chem, Kohoku Ku, Yokohama, Kanagawa 2238522, Japan
Yamada, T
[1
]
机构:
[1] Keio Univ, Fac Sci & Technol, Dept Chem, Kohoku Ku, Yokohama, Kanagawa 2238522, Japan
来源:
SYNTHESIS-STUTTGART
|
2004年
/
12期
关键词:
aldehyde;
asymmetric catalysis;
salen-cobalt complexes;
direct nitroaldol reaction;
beta-hydroxynitroalkanes;
D O I:
10.1055/s-2004-829157
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
The enantioselective Henry reaction catalyzed by the optically active salen-cobalt complexes, proceeded to afford beta-hydroxynitroalkanes in good-to-high yields with high enantioselectivity.