Opportunities and challenges in synthetic oligosaccharide and glycoconjugate research
Top Cited Papers
- 23 October 2009
- journal article
- review article
- Published by Springer Nature in Nature Chemistry
- Vol. 1 (8) , 611-622
- https://doi.org/10.1038/nchem.399
Abstract
The development of general synthetic strategies for the prepartion of oligonucleotides and peptides has enabled them to be made routinely — often using automated systems. Making complex oligosaccharides is much less straightforward, but advances in areas such as one-pot multi-step protecting-group manipulations, stereoselective glycosylation protocols and chemo-enzymatic methods are offering new opportunities for carbohydrate chemistry. Synthetic oligosaccharides and glycoconjugates are increasingly used as probes for biological research and as lead compounds for drug and vaccine discovery. These endeavours are, however, complicated by a lack of general methods for the routine preparation of these important compounds. Recent developments such as one-pot multistep protecting-group manipulations, the use of unified monosaccharide building blocks, the introduction of stereoselective glycosylation protocols, and convergent strategies for oligosaccharide assembly, are beginning to address these problems. Furthermore, oligosaccharide synthesis can be facilitated by chemo-enzymatic methods, which employ a range of glycosyl transferases to modify a synthetic oligosaccharide precursor. Glycosynthases, which are mutant glycosidases, that can readily form glycosidic linkages are addressing a lack of a wide range of glycosyltransferases. The power of carbohydrate chemistry is highlighted by an ability to synthesize glycoproteins.Keywords
This publication has 123 references indexed in Scilit:
- Toward Homogeneous Erythropoietin: Fine Tuning of the C-Terminal Acyl Donor in the Chemical Synthesis of the Cys29−Gly77 Glycopeptide DomainJournal of the American Chemical Society, 2009
- Synthesis and Applications of a Light-Fluorous Glycosyl DonorThe Journal of Organic Chemistry, 2009
- Combinatorial Chemoenzymatic Synthesis and High-Throughput Screening of SialosidesACS Chemical Biology, 2008
- Stereoselective Iterative One-Pot Synthesis ofN-Glycolylneuraminic Acid-Containing OligosaccharidesOrganic Letters, 2008
- Synthetic Studies toward Mycobacterium tuberculosis Sulfolipid-IThe Journal of Organic Chemistry, 2008
- Multi-Component One-Pot Synthesis of the Tumor-Associated Carbohydrate Antigen Globo-H Based on Preactivation of Thioglycosyl DonorsThe Journal of Organic Chemistry, 2007
- Synthesis and medical applications of oligosaccharidesNature, 2007
- Heparan sulphate proteoglycans fine-tune mammalian physiologyNature, 2007
- Chemical glycosylation in the synthesis of glycoconjugate antitumour vaccinesNature, 2007
- Stereoselective Glycosylations of 2-Azido-2-deoxy-glucosides Using Intermediate Sulfonium IonsOrganic Letters, 2007