Supporting Information
| Supporting Information File 1: Experimental procedures; experimental data for synthesized compounds; competitive glycosylation of O- and S-nucleophiles; problematic glycosyl acceptors; reaction optimization data; reactivity of other glycosyl donors; proposed structures of side-products; detailed description of 19F NMR studies; stability tests for various glycosyl donors. | ||
| Format: PDF | Size: 2.6 MB | Download |
| Supporting Information File 2: Copies of NMR spectra. | ||
| Format: PDF | Size: 21.3 MB | Download |
| Supporting Information File 3: DFT calculations. | ||
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Cite the Following Article
Metal-free glycosylation with glycosyl fluorides in liquid SO2
Krista Gulbe, Jevgeņija Lugiņina, Edijs Jansons, Artis Kinens and Māris Turks
Beilstein J. Org. Chem. 2021, 17, 964–976.
https://doi.org/10.3762/bjoc.17.78
How to Cite
Gulbe, K.; Lugiņina, J.; Jansons, E.; Kinens, A.; Turks, M. Beilstein J. Org. Chem. 2021, 17, 964–976. doi:10.3762/bjoc.17.78
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