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As far as we are aware, the only reference concerning β-amino-β-ferrocenyl carbonyl derivatives describes the low-yield (15%) formation of rac-4-ferrocenyl-4-(2-naphthyl)aminobutanone in the reaction between (2-naphthyl)ferrocenylimine and acetone catalyzed by p-toluenesulfonic acid. See: Kalenikov, E. A. Zh. Obshch. Khim. 1977, 43, 628.
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As far as we are aware, the only reference concerning β-amino-β-ferrocenyl carbonyl derivatives describes the low-yield (15%) formation of rac-4-ferrocenyl-4-(2-naphthyl)aminobutanone in the reaction between (2-naphthyl)ferrocenylimine and acetone catalyzed by p-toluenesulfonic acid. See: Kalenikov, E. A. Zh. Obshch. Khim. 1977, 43, 628.
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When, under the same reaction conditions, the p-methoxy- phenylimine of benzaldehyde was reacted with butanone, a 1:1.2 mixture of diastereomers (linear/branched) was obtained.
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When, under the same reaction conditions, the p-methoxy- phenylimine of benzaldehyde was reacted with butanone, a 1:1.2 mixture of diastereomers (linear/branched) was obtained.
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