Studies in oligosaccharide chemistry. Part 8. Synthesis of lacto-N-triose I, a core chain trisaccharide of human blood-group substances
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1977/P1/P19770001343
Cited by 20 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Synthesis of lacto-N-neotetraose and lacto-N-tetraose using the dimethylmaleoyl group as amino protective group;Carbohydrate Research;1999-03
2. G;Dictionary of Carbohydrates;1998
3. A convenient synthesis of lacto-N-biose I [β-d-Galp-(1 → 3)-β-d-GlcpNAc] linked oligosaccharides from phenyl O-(tetra-O-acetyl-β-d-galactopyranosyl)-(1 → 3)-4,6-di-O-acetyl-2-deoxy-2-phthalimido-1-thio-β-d-glucopyranoside;Carbohydrate Research;1993-03
4. Efficient catalysis by pyridinium sulfonate in glycosylation involving an oxazoline intermediate derived from per-O-acetyl-N-acetyllactosamine andN,N?-diacetylchitobiose;Glycoconjugate Journal;1992-12
5. Synthesis of oligosaccharides of 2-amino-2-deoxy sugars;Chemical Reviews;1992-09
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