首页> 外文期刊>Tetrahedron, Asymmetry: The International Journal for Repid Publication on all Aspects of Asymmetry in Orgainc, Inorganic, Organometallic, Physical and Bio-Organic Chemistry >Synthesis of chiral non-racemic azetidines by lipase-catalysed acetylations and their transformation into amino alcohols: precursors of chiral catalysts
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Synthesis of chiral non-racemic azetidines by lipase-catalysed acetylations and their transformation into amino alcohols: precursors of chiral catalysts

机译:脂肪酶催化乙酰化手性非外消旋氮杂环丁烷的合成及其向氨基醇的转化:手性催化剂的前体

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摘要

Azetidinic mono-acetate 7, diol 6b and di-acetate 10a were prepared with high e.e. using PPL-catalysed acetylations. The absolute configurations of all new enantioenriched compounds were assigned by chemical correlation with known compounds. Mono-acetate 7 was then transformed into 30, an amino alcohol of noteworthy potential interest since it represents an interesting precursor for chiral catalysts, such as 32. (C) 2001 Elsevier Science Ltd. All rights reserved. [References: 41]
机译:制备具有高e.e.的氮杂环丁烷单乙酸盐7,二醇6b和二乙酸盐10a。使用PPL催化的乙酰化作用。通过与已知化合物的化学相关性分配所有新的对映体富集的化合物的绝对构型。然后将单乙酸酯7转化为30,这是值得关注的潜在氨基醇,因为它代表了手性催化剂的令人感兴趣的前体,例如32。(C)2001 Elsevier Science Ltd.保留所有权利。 [参考:41]

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