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Novel Cinchona alkaloid derived ammonium salts as catalysts for the asymmetric synthesis of β-hydroxy α-amino acids via aldol reactions

机译:新型金鸡纳生物碱衍生的铵盐作为通过醛醇缩合反应不对称合成β-羟基α-氨基酸的催化剂

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摘要

Using the cinchonidine-derived phase-transfer catalyst de veloped by Park and Jew as a lead structure, we have prepared novel chiral ammonium salts and investigated their efficacy for the preparation of β-hydroxy α-amino acids via asymmetric aldol reactions. The modifications were performed at C3 of the cinchonidine nucleus and include dimers as well as catalysts possessing electron-deficient alkyne and alkene moieties. Some of the new catalysts yielded improvements relative to the Park–Jew catalyst in the aldol reaction.
机译:以Park和Jew开发的辛可尼定衍生的相转移催化剂为主导结构,我们制备了新型手性铵盐,并研究了其通过不对称醛醇缩合反应制备β-羟基α-氨基酸的功效。修饰是在辛可尼定核的C3处进行的,包括二聚体以及具有缺电子炔烃和烯烃基团的催化剂。相对于Park-Jew催化剂在醛醇缩合反应中,某些新型催化剂产生了改进。

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