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首页> 外文期刊>Chemical Communications >Highly stereoselective intramolecular α-arylation of self-stabilized non-racemic enolates: synthesis of α-quaternary α-amino acid derivatives
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Highly stereoselective intramolecular α-arylation of self-stabilized non-racemic enolates: synthesis of α-quaternary α-amino acid derivatives

机译:自稳定的非外消旋烯酸酯的高度立体选择性分子内α-芳基化:α-季α-氨基酸衍生物的合成

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摘要

The 'one-pot' stereoselective conversion of N-(4-nitrobenzene)-sulfonyl-α-amino acid tert-butyl esters into the corresponding N-alkyl-α-(4-nitrophenyl)-α-amino esters has been realized through N-alkylation of the starting amido esters, followed by N-C_α migration of the p-nitrophenyl group and the loss of sulfur dioxide; the asymmetric induction is determined by an intermediate non-racemic enolate, without the need of an external source of chitality.
机译:通过以下方法实现了N-(4-硝基苯)-磺酰基-α-氨基酸叔丁酯的``一锅''立体选择性转化为相应的N-烷基-α-(4-硝基苯基)-α-氨基酯起始酰胺基酯的N-烷基化,随后对硝基苯基的N-C_α迁移和二氧化硫的损失;不对称诱导是由中间非外消旋烯醇决定的,不需要外部的手性来源。

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  • 来源
    《Chemical Communications 》 |2009年第33期| 5012-5014| 共3页
  • 作者单位

    Nerviano Medical Sciences, Viale Pasteur 10,1-20014 Nerviano, Italy Dipartimento di Chimica Organica e Industriale, Universita degli Studi, Via Venezian 21, I-20133 Milano, Italy;

    CNR Institute of Molecular Science and Technologies (ISTM),Via Golgi 19, I-20133 Milano, Italy;

    Dipartimento di Chimica Organica e Industriale, Universita degli Studi, Via Venezian 21, I-20133 Milano, Italy;

    Dipartimento di Chimica Organica e Industriale, Universita degli Studi, Via Venezian 21, I-20133 Milano, Italy;

    Dipartimento di Chimica Organica e Industriale, Universita degli Studi, Via Venezian 21, I-20133 Milano, Italy;

    Dipartimento di Chimica Organica e Industriale, Universita degli Studi, Via Venezian 21, I-20133 Milano, Italy;

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