首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Novel Cinchona alkaloid derived ammonium salts as catalysts for the asymmetric synthesis of beta-hydroxy alpha-amino acids via aldol reactions
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Novel Cinchona alkaloid derived ammonium salts as catalysts for the asymmetric synthesis of beta-hydroxy alpha-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 developed by Park and Jew as a lead structure,we have prepared novel chiral ammonium salts and investigated their efficacy for the preparation of p-hydroxy alpha-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,并研究了它们通过不对称醛醇缩合反应制备对羟基α-氨基酸的功效。在辛可尼定核的C3处,包括二聚体以及具有缺电子炔烃和烯烃部分的催化剂。

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