4.8 Article

Ni/Photoredox-Dual-Catalyzed Functionalization of 1-Thiosugars

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ORGANIC LETTERS
卷 21, 期 13, 页码 5132-5137

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b01730

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资金

  1. ANR (CarNuCat) [ANR-15-CE29- 0002]
  2. la Ligue Contre le Cancer through an Equipe Labellisee 2014 grant
  3. China Scholarship Council
  4. Laboratory of Excellence CHARMMMAT
  5. CNRS
  6. University Paris-Sud
  7. [ANR-10-LABX-33]
  8. Agence Nationale de la Recherche (ANR) [ANR-15-CE29-0002] Funding Source: Agence Nationale de la Recherche (ANR)

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A general protocol for functionalization of glycosyl thiols has been reported. This protocol is based on a single-electron Ni/photoredox dual-catalyzed cross coupling between 1-thiosugars and a broad range of aryl bromides and iodides as well as alkenyl and alkynyl halides. This base-free method gives access to a series of functionalized thioglycosides in moderate to excellent yields with a perfect control of the anomeric configuration. Moreover, it has been shown that this methodology may be transposed successfully to the continuous-flow photoredox chemistry.

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