Abstract
C -aryl glycosides have attracted considerable interest as biologically active natural products and as O -aryl glycoside mimetics in drug discovery. Here, we describe a straightforward synthesis of C -aryl glycosides via photoredox/Ni dual-catalyzed reductive cross-coupling between glycosyl bromides and aryl bromides. This methodology enables highly α-stereoselective synthesis of C -aryl-glucosides, galactosides, and mannosides.
Original language | English |
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Journal | Synlett |
DOIs | |
Publication status | Accepted/In press - 2024 |
All Science Journal Classification (ASJC) codes
- Organic Chemistry