SELENIUM-MEDIATED GLYCOSIDATIONS: A SELECTIVE SYNTHESIS OF β-2-DEOXYGLYCOSIDES

DOI: 10.1016/S0040-4039(01)80327-0

Source and publish data:

Tetrahedron Letters p. 75 - 78 (1989)

Update date:2022-09-26

Topics:

Authors:

Perez, Michel

Beau, Jean-Marie

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Article abstract of DOI:10.1016/S0040-4039(01)80327-0

1,2-Trans diequatorial acetoxy-selenides are selectively prepared from glycals.Their activation by trimethylsilyl trifluoromethanesulfonate in the presence of sugar alcohols followed by reductive deselenation leads to an efficient access to Β-2-deoxyglyco

Full text of DOI:10.1016/S0040-4039(01)80327-0

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