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Glycosylations diphenyl sulfoxide

A conceptually new direct oxidative glycosylation with glycal donors, employing a reagent combination of triflic anhydride and diphenyl sulfoxide, has recently been reported by Gin [83], This new 3-glycosylation method works very well with hindered hydroxy nucleophiles, including sterically shielded carbohydrate hydroxy systems, and can be run on large scales. [Pg.302]

Representative Procedure for Diphenyl Sulfoxide and Triflic Anhydride Promoted Glycosylation with Cl-Hemiacetal Donors 130... [Pg.8]

Garcia, B A, Poole, J L, Gin, D Y, Direct glycosylations with 1-hydroxy glycosyl donors using trifluoromethanesulfonic anhydride and diphenyl sulfoxide, J. Am. Chem. Soc., 119, 7597-7598, 1997. [Pg.189]


See other pages where Glycosylations diphenyl sulfoxide is mentioned: [Pg.256]    [Pg.256]    [Pg.128]    [Pg.128]    [Pg.252]    [Pg.268]    [Pg.142]    [Pg.174]    [Pg.147]    [Pg.179]    [Pg.43]    [Pg.66]    [Pg.128]    [Pg.121]    [Pg.515]    [Pg.515]    [Pg.145]    [Pg.256]    [Pg.258]    [Pg.258]    [Pg.590]    [Pg.590]    [Pg.216]    [Pg.32]   
See also in sourсe #XX -- [ Pg.256 ]




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Glycosyl sulfoxides

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