首页> 外文会议>European Symposium on Organic Chemistry >Diastereoselective aldolization with reputed unstable enolates : Synthesis of chiral α-amino-β-hydroxy acids , aminodiols or diaminoalcohols
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Diastereoselective aldolization with reputed unstable enolates : Synthesis of chiral α-amino-β-hydroxy acids , aminodiols or diaminoalcohols

机译:具有众所律的不稳定烯醇化合物的非对映选择性醛固化:合成手性α-氨基-β-羟基酸,氨基二醇或二氨基醇

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摘要

Syn α-Amino-β-hydroxy acids are the key structures of many natural products exhibiting a wide range of biological activities. For example, syn α-amino-β-hydroxy acids are found in vancomycin or polyoxins (antibiotics), cyclomarins (cytotoxic, antiinflammatory), ustiloxins (antibiotic, antimitotic), and exochelins (iron chelator). Many studies have been devoted to the synthesis of this unit and most of them rely on an aldol reaction between a glycine equivalent and an aldehyde.
机译:SYNα-氨基-β-羟基酸是许多天然产品的关键结构,其具有广泛的生物活性。例如,SYNα-氨基-β-羟基酸在万古霉素或聚霉素(抗生素),单胞苷(细胞毒性,抗炎),Ustiloxins(抗生素,抗氨酸)和外脱蛋白(铁螯合剂)中。许多研究已经致力于该单位的合成,并且大多数依赖于甘氨酸当量和醛之间的醛醇反应。

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