| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0008-6215(99)00080-4 |
| P698 | PubMed publication ID | 10515050 |
| P2093 | author name string | R Roy | |
| S Cao | |||
| Z Gan | |||
| P2860 | cites work | Chemoselective Glycosylations. 2. Differences in Size of Anomeric Leaving Groups Can Be Exploited in Chemoselective Glycosylations | Q47200246 |
| Vinyl Glycosides in Oligosaccharide Synthesis. 2. The Use of Allyl and Vinyl Glycosides in Oligosaccharide Synthesis | Q57242648 | ||
| Chemoselective glycosylations (part 1): Differences in size of anomeric leaving groups can be exploited in chemoselective glycosylations | Q57242654 | ||
| Vinyl glycosides in oligosaccharide synthesis (part 1): A new latent-active glycosylation strategy | Q57242657 | ||
| Total synthesis of sulfated Le(x) pentaosyl ceramide | Q72368601 | ||
| Synthesis of sialyl Le(x) ganglioside analogues sulfated at C-6 of either the galactose or N-acetylglucosamine residues, and at both of the galactose and N-acetylglucosamine residues: probes for clarifying the real carbohydrate ligand of L-selectin | Q73019576 | ||
| P433 | issue | 1-4 | |
| P304 | page(s) | 75-81 | |
| P577 | publication date | 1999-05-01 | |
| P1433 | published in | Carbohydrate Research | Q2937927 |
| P1476 | title | Active-latent glycosylation strategy toward Lewis X pentasaccharide in a form suitable for neoglycoconjugate syntheses | |
| P478 | volume | 318 |
| Q33853098 | Convergent syntheses of Le analogues |
| Q33788978 | First principles insight into the alpha-glucan structures of starch: their synthesis, conformation, and hydration |
| Q61455356 | Polymer-supported and chemoenzymatic synthesis of the Neisseria meningitidis pentasaccharide: a methodological comparison |
| Q36218343 | Studies on the Selectivity Between Nickel-Catalyzed 1,2-cis-2-Amino Glycosylation of Hydroxyl Groups of Thioglycoside Acceptors with C(2)-Substituted Benzylidene N-Phenyl Trifluoroacetimidates and Intermolecular Aglycon Transfer of the Sulfide Group |
| Q36281169 | Synthesis of 4” manipulated Lewis X trisaccharide analogues |
| Q47415509 | Synthesis of LewisX-O-Core-1 threonine: A building block for O-linked LewisX glycopeptides |
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