Use of dichlorophthaloyl (DCPhth) group as an amino protecting group in oligosaccharide synthesis

[1]  M. Kiso,et al.  Synthesis of deoxygalactose-containing sialyl LeX ganglioside analogues to elucidate the structure necessary for selectin recognition , 1996, Glycoconjugate Journal.

[2]  Y. Ito,et al.  4,5-dichlorophthaloyl group for amino protection in carbohydrate chemistry. , 1996, Bioscience, biotechnology, and biochemistry.

[3]  R. Schmidt,et al.  N-Tetrachlorophthaloyl-protected trichloroacetimidate of glucosamine as glycosyl donor in oligosaccharide synthesis , 1995 .

[4]  R. Madsen,et al.  Two New Orthogonal Amine-Protecting Groups that can be Cleaved under Mild or Neutral Conditions , 1995 .

[5]  R. Roy,et al.  Mild stereoselective syntheses of thioglycosides under PTC conditions and their use as active and latent glycosyl donors , 1994 .

[6]  X. Pannecoucke,et al.  Synthesis of phosphoric acid diesters of 7β- hydroxycholesterol and of carbohydrates , 1994 .

[7]  R. Schmidt,et al.  Efficient sialylation with phosphite as leaving group , 1992 .

[8]  J. Banoub,et al.  Synthesis of oligosaccharides of 2-amino-2-deoxy sugars , 1992 .

[9]  M. Kiso,et al.  A facile, large-scale preparation of the methyl 2-thioglycoside of N-acetylneuraminic acid, and its usefulness for the alpha-stereoselective synthesis of sialoglycosides. , 1991, Carbohydrate research.

[10]  M. Kiso,et al.  Communication: Synthetic Studies on Sialoglycoconjugates 25: Reactivity of Glycosyl Promoters in α-Glycosylation of N-Acetyl-Neuraminic Acid with the Primary and Secondary Hydroxyl Groups in the Suitably Protected Galactose and Lactose Derivatives , 1991 .

[11]  T. Fukuyama,et al.  p-Anisyl group: A versatile protecting group for primary alcohols , 1985 .

[12]  E. Anet 6-O-benzyl-D-galactose and its dimethyl acetal , 1968 .