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- Title
Copper‐Catalyzed Stereoselective Borylation and Palladium‐Catalyzed Stereospecific Cross‐Coupling to Give Aryl C‐Glycosides.
- Authors
Kurahayashi, Kazuki; Hanaya, Kengo; Sugai, Takeshi; Hirai, Go; Higashibayashi, Shuhei
- Abstract
Metabolically stable C‐glycosides are an essential family of compounds in bioactive natural products, therapeutic agents, and biological probes. For their application, development of synthetic methods by connecting glycosides and aglycons with strict stereocontrol at the anomeric carbon, as well as with high functional‐group compatibility and environmental compatibility is a pivotal issue. Although Suzuki–Miyaura‐type C(sp3)−C(sp2) cross‐coupling using glycosyl boronates is a potential candidate for the construction of C‐glycosides, neither the cross‐coupling itself nor the facile synthesis of the coupling precursor, glycosyl boronates, have been achieved to date. Herein, it was succeeded to develop a copper‐catalyzed stereoselective one‐step borylation of glycosyl bromides to glycosyl boronates and palladium‐catalyzed stereospecific cross‐coupling of β‐glycosyl borates with aryl bromides to give aryl β‐C‐glycosides, in which the β‐configuration of the anomeric carbon of the glycosyl trifluoroborates is stereoretentively transferred to that of the resulting aryl C‐glycosides.
- Subjects
BORYLATION; BIOACTIVE compounds; SONOGASHIRA reaction; ARYL bromides; NATURAL products; BORATES
- Publication
Chemistry - A European Journal, 2023, Vol 29, Issue 6, p1
- ISSN
0947-6539
- Publication type
Article
- DOI
10.1002/chem.202203376