期刊
CHEMICAL COMMUNICATIONS
卷 56, 期 52, 页码 7175-7178出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0cc02175j
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资金
- CNRS, Universite Paris-Saclay
- ANR (SelFSuCHi) [ANR-18-CE07-0012]
- Ecole Polytechnique, la Ligue Contre le Cancer through an Equipe Labellisee 2014 grant
- [ANR-10-LABX-33]
- Agence Nationale de la Recherche (ANR) [ANR-18-CE07-0012] Funding Source: Agence Nationale de la Recherche (ANR)
An efficient regio- and diastereoselective arylation method of readily available 2,3-glycals with various aryl iodides has been established. Using the Pd(OAc)(2)/AsPh(3)precatalytic system, this protocol proved to be general to prepare a variety of substituted C2-aryl glycosides in good yields with complete diastereoselectivity.
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