Direct β-alkylation of secondary alcohols with primary alcohols catalyzed by a Cp*lr complex
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Fujita, K
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Kyoto Univ, Grad Sch Human & Environm Studies, Sakyo Ku, Kyoto 6068501, JapanKyoto Univ, Grad Sch Human & Environm Studies, Sakyo Ku, Kyoto 6068501, Japan
Fujita, K
[1
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Asai, C
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Kyoto Univ, Grad Sch Human & Environm Studies, Sakyo Ku, Kyoto 6068501, JapanKyoto Univ, Grad Sch Human & Environm Studies, Sakyo Ku, Kyoto 6068501, Japan
Asai, C
[1
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Yamaguchi, T
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Kyoto Univ, Grad Sch Human & Environm Studies, Sakyo Ku, Kyoto 6068501, JapanKyoto Univ, Grad Sch Human & Environm Studies, Sakyo Ku, Kyoto 6068501, Japan
Yamaguchi, T
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]
Hanasaka, F
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Kyoto Univ, Grad Sch Human & Environm Studies, Sakyo Ku, Kyoto 6068501, JapanKyoto Univ, Grad Sch Human & Environm Studies, Sakyo Ku, Kyoto 6068501, Japan
Hanasaka, F
[1
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Yamaguchi, R
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Kyoto Univ, Grad Sch Human & Environm Studies, Sakyo Ku, Kyoto 6068501, JapanKyoto Univ, Grad Sch Human & Environm Studies, Sakyo Ku, Kyoto 6068501, Japan
Yamaguchi, R
[1
]
机构:
[1] Kyoto Univ, Grad Sch Human & Environm Studies, Sakyo Ku, Kyoto 6068501, Japan
A new catalytic system for beta-alkylation of secondary alcohols has been developed. In the presence of [Cp*IrCl2](2) (CP* = pentamethylcyclopentadienyl) catalyst and base, the reactions of various secondary alcohols with primary alcohols give beta-alkylated higher alcohols in good to excellent yields without any hydrogen acceptor or hydrogen donor. This reaction proceeds via successive hydrogen-transfer reactions and aldol condensation.