By David C. Baker, Derek Horton
Advances in Carbohydrate Chemistry and Biochemistry, a part of an extended working serial that started in 1945, presents serious and informative articles written by way of study experts that combine the commercial, analytical, and technological features of biochemistry, natural chemistry, and instrumentation method within the examine of carbohydrates. each one article offers a definitive interpretation of the present prestige and destiny traits in carbohydrate chemistry and biochemistry.
- Features contributions from best professionals and specialists who specialise in carbohydrate chemistry, biochemistry, and research
- Integrates the commercial, analytical, and technological facets of biochemistry, natural chemistry, and instrumentation technique within the examine of carbohydrates
- Informs and updates on the entire most recent advancements within the box
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Extra resources for Advances in Carbohydrate Chemistry and Biochemistry, Volume 72
H. Chemical Approaches to Define the Structure-Activity Relationship of Heparin-Like Glycosaminoglycans. Chem. Biol. 2005, 12, 731–756. 24. van den Bos, L. ; Code´e, J. D. ; Litjens, R. E. J. ; Overkleeft, H. ; van der Marel, G. A. Uronic Acids in Oligosaccharide Synthesis. Eur. J. Org. Chem. 2007, 3963–3976. 25. Dulaney, S. ; Huang, X. Strategies in Synthesis of Heparin/Heparan Sulfate Oligosaccharides: 2000–Present. Adv. Carbohydr. Chem. Biochem. 2012, 67, 95–136. 26. Zulueta, M. M. -C. Synthetic Heparin and Heparan Sulfate Oligosaccharides and Their Protein Interactions.
42 Shifaza Mohamed and Vito Ferro subjected to sodium borohydride reduction. The reduction proceeded with excellent stereoselectivity to give the corresponding alcohol in 91% diastereoselectivity, which was protected as the triethylsilyl ether prior to the removal of the thiazole ring. The fully protected compound 89 was then subjected to thiazole to formyl deblocking to obtain the protected aldehyde 90. 118 L-Idose can be formally converted into various IdoA derivatives for use in GAG synthesis, although there have been no reports of the utilization of the above method for this purpose, perhaps due to the relatively high cost of the L-xylose starting material.
Eur. J. 2010, 16, 8365–8375. ; Huang, X. Divergent Heparin Oligosaccharide Synthesis with Pre-installed Sulfate Esters. Chem. Eur. J. 2011, 17, 10106–10112.