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

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.
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Supporting Information File 2: Copies of NMR spectra.
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Supporting Information File 3: DFT calculations.
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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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