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β-Amidoaldehydes via oxazoline hydroformylation

机译:通过恶唑啉加氢甲酰化的β-氨基醛

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摘要

4-Substituted oxazolines, which are readily synthesized from naturally occurring α-amino acids, are converted efficiently and stereospecifically to β-amidoaldehydes in the presence of synthesis gas and catalytic dicobalt octacarbonyl. Enantiomerically pure N-protected β-aminoaldehydes are useful building blocks for addition of β-amino functionality in a stereospecific fashion. This method has been utilized for the synthesis of β-peptide derivatives as well as other bioactive molecules.
机译:由天然存在的α-氨基酸容易合成的4-取代的恶唑啉在合成气和催化二羰八羰基化合物的存在下有效且立体定向地转化为β-酰胺醛。对映体纯的N-保护的β-氨基醛是用于以立体特异性方式添加β-氨基官能团的有用的结构单元。该方法已经用于合成β-肽衍生物以及其他生物活性分子。

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  • 来源
    《Chemical Communications》 |2009年第38期|5704-5706|共3页
  • 作者单位

    Department of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, NY 14853-1301, USA;

    Department of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, NY 14853-1301, USA;

    Department of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, NY 14853-1301, USA;

    Department of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, NY 14853-1301, USA;

    Department of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, NY 14853-1301, USA;

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  • 入库时间 2022-08-17 13:25:57

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