| Literature DB >> 29573308 |
Audrey Dumoulin1, Jennifer K Matsui1, Álvaro Gutiérrez-Bonet1, Gary A Molander1.
Abstract
The development of synthetic tools to introduce saccharide derivatives into functionally complex molecules is of great interest, particularly in the field of drug discovery. Herein, we report a new route toward highly functionalized, arylated saccharides, which involves nickel-catalyzed cross-coupling of photoredox-generated saccharyl radicals with a range of aryl- and heteroaryl bromides, triggered by an organic photocatalyst. In contrast to existing methods, the mild reaction conditions achieve arylation of saccharide motifs while leaving the anomeric carbon available, thus providing access to a class of arylated glycosides that has been underexplored until now. To demonstrate the potential of this strategy in late-stage functionalization, a variety of structurally complex molecules incorporating saccharide moieties were synthesized.Entities:
Keywords: 1,4-dihydropyridines; glycosylation; homogeneous catalysis; nickel; photoredox chemistry
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Year: 2018 PMID: 29573308 PMCID: PMC6540763 DOI: 10.1002/anie.201802282
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336