μ‐Oxo‐Dinuclear‐Iron(III)‐Catalyzed O‐Selective Acylation of Aliphatic and Aromatic Amino Alcohols and Transesterification of Tertiary Alcohols |
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Authors: | Rikiya Horikawa Chika Fujimoto Dr. Ryo Yazaki Prof. Dr. Takashi Ohshima |
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Affiliation: | Graduate school of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan |
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Abstract: | A highly chemoselective and reactive μ‐oxo‐dinuclear iron(III) salen catalyst for transesterification was developed. The developed iron complex catalyzed acylation of aliphatic amino alcohols with nearly perfect O‐selectivity, even when using activated esters, for which chemoselectivity is more difficult to control. In addition, O‐selective transesterification of aromatic amino alcohols was achieved for the first time. The high activity of the iron complex enabled the use of sterically congested tertiary alcohols, including unprecedented tert‐butanol. |
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Keywords: | alcohols chemoselectivity iron tert-butyl ester transesterification |
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