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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >An efficient synthesis of gamma-amino beta-ketoester by cross-Claisen condensation with alpha-amino acid derivatives
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An efficient synthesis of gamma-amino beta-ketoester by cross-Claisen condensation with alpha-amino acid derivatives

机译:通过与α-氨基酸衍生物的交叉克莱森缩合反应有效地合成γ-氨基β-酮酸酯

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摘要

Cross-ester condensation between N-protected amino acid ester and the lithium enolate prepared from alyl acetate gave the corresponding beta-ketoester in high yield without the formation of the tertiary alcohol that is commonly seen as by-product. This interesting reaction is applicable to the amino acid derivatives with suitable N-protecting groups, which can help to stabilize and reaction intermediates.
机译:N-保护的氨基酸酯和由乙酸烷基酯制得的烯醇锂之间的交叉酯缩合以高产率得到相应的β-酮酯,而没有形成通常被视为副产物的叔醇。该有趣的反应适用于具有合适的N-保护基的氨基酸衍生物,其可以帮助稳定中间体。

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