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Glycosyl fluoride method, stereoselective

The classical method for introducing the fluorine atom to the anomeric center is to treat per-O-acetylated sugars with hydrogen fluoride [15], using which a-glycosyl fluorides can be prepared stereoselectively, however, the procedure is incompatible with any acid-sensitive functionalities present in the molecule. In addition, hydrogen fluoride is highly corrosive, which makes this method unattractive to many... [Pg.53]

See other pages where Glycosyl fluoride method, stereoselective is mentioned: [Pg.348] [Pg.37] [Pg.317] [Pg.411] [Pg.138] [Pg.143] [Pg.237] [Pg.593] [Pg.496] [Pg.543] [Pg.580] [Pg.496] [Pg.543] [Pg.14] [Pg.62] [Pg.26] [Pg.157] [Pg.306] [Pg.134] [Pg.85] [Pg.222] [Pg.85] [Pg.222] [Pg.133] [Pg.309] [Pg.11] [Pg.492] [Pg.492] [Pg.15] [Pg.1151]

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Glycosyl fluoride method

Glycosyl fluoride method, stereoselective glycosylation

Glycosyl fluorides fluoride)

Glycosyl fluorides glycosylations

Glycosylation methods

Glycosylation stereoselectivity

Glycosylation, glycosyl fluorides

Glycosylations glycosylation Stereoselective

Glycosylations methods

Stereoselective glycosylation