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Catalytic asymmetric synthesis of 5-membered alicyclic α-quaternary β-amino acids via [3 + 2]-photocycloaddition of α-substituted acrylates

机译:α取代丙烯酸酯的催化不对称合成5-元脂环族α-季β-氨基酸的α-取代丙烯酸酯

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摘要

The photocatalytically active salt of a cationic iridium polypyridyl complex and a chiral borate is competent to promote a highly stereoselective [3 + 2]-cycloaddition of cyclopropylurea with a-substituted acrylates. This protocol provides straightforward access to a variety of stereochemically defined 5-membered alicyclic a-quaternary p-amino acids, useful building blocks of p-peptides and peptidomimetics.
机译:阳离子铱萘吡啶络合物和手性硼酸盐的光催化活性盐是促进与取代的丙烯酸酯的高度立体切选择[3 + 2] -Cycloaddition的环丙基。该方案提供对各种立体化学定义的5-元脂环族A-季氨基氨基酸的直接进入,P-肽和拟肽模拟物的有用构件块。

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  • 来源
    《Organic & biomolecular chemistry》 |2021年第8期|1744-1747|共4页
  • 作者单位

    Institute of Transformative Bio-Molecules (WPI-ITbM) and Department of Molecular and Macromolecular Chemistry Graduate School of Engineering Nagoya University Nagoya 464-8601 Japan;

    Institute for Catalysis Hokkaido University Sapporo 001-0021 Japan;

    Institute of Transformative Bio-Molecules (WPI-ITbM) and Department of Molecular and Macromolecular Chemistry Graduate School of Engineering Nagoya University Nagoya 464-8601 Japan;

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