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Synthesis and photoinitiated thiol-ene reactions ofexo-mannals - a new route toC-beta-d-mannosyl derivatives

机译:opro-momnals的合成和光灭绝的硫醇 - 烯丙基反应 - 一种新的TOC-β-D-甘露糖基衍生物

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摘要

Syntheses of acyl protectedexo-mannal derivatives were developed starting fromO-peracylated mannopyranosesviathe corresponding anhydro-aldose tosylhydrazones under modified Bamford-Stevens conditions. The synthesis of analogousO-peralkylated (benzylated and isopropylenated) derivatives was carried out from pyranoid and furanoid mannonolactones using methylene transfer reagents. Photoinitiated thiol-ene additions of theseexo-mannals resulted in the correspondingC-(mannopyranosyl/mannofuranosyl)methyl sulfides in medium to good yields with exclusive regio- and beta(d) stereoselectivities.
机译:酰基抗保护性甲状腺衍生物的合成是从修饰Bamford-stevens条件下的相应的羟基醛吡喃萘葡萄酒开始起始。 使用亚甲基转移试剂从吡喃醇和呋喃醇甘油酮中进行类似替代氟烷基化(苄化和异丙基)衍生物的合成。 光引出的硫醇-NEE添加到的TheSexo-Mornals导致相应的 - (甘露糖糖基/甘露胶溶胶基)甲基硫醚中的培养基与良好的产率,具有专用的regio-和β(d)立体切性。

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  • 来源
    《RSC Advances》 |2020年第57期|共12页
  • 作者单位

    Univ Debrecen Dept Organ Chem POB 400 H-4002 Debrecen Hungary;

    Univ Debrecen Dept Pharmaceut Chem POB 400 H-4002 Debrecen Hungary;

    Univ Debrecen Dept Pharmaceut Chem POB 400 H-4002 Debrecen Hungary;

    Univ Debrecen Dept Pharmaceut Chem POB 400 H-4002 Debrecen Hungary;

    Univ Debrecen Dept Organ Chem POB 400 H-4002 Debrecen Hungary;

    Univ Debrecen Dept Organ Chem POB 400 H-4002 Debrecen Hungary;

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  • 正文语种 eng
  • 中图分类 化学;
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