Download Frontiers in Modern Carbohydrate Chemistry by Alexei V. Demchenko (Eds.) PDF

By Alexei V. Demchenko (Eds.)

content material: Synthesis of 9-substituted sialic acids as probes for CD22-ligand interactions on B cells / Shoufa Han, Brian E. Collins, and James C. Paulson --
unusual sugars and their conjugates to common items / Wenlan Chen ... [et al.] --
Plant mobilephone wall glycans : chemical synthesis of the branched sugar aceric acid / Sergey A. Nepogodiev, Nigel A. Jones, and Robert A. box --
Iodoamidation of glycals : a facile practise of 2-deoxy-N-glycosylamides / Cecilia H. Marzabadi and Michael DeCastro --
Stereocontrolled glycosylation : fresh advances : [beta]-D-rhamnosides and [beta]-D-mannans / David Crich --
Stereoselective glycosylations utilizing chiral auxiliaries / Jin-Hwan Kim, Hai Yang, and Geert-Jan Boons --
keeping teams in carbohydrate chemistry profoundly impact all selectivities in glycosyl couplings / Bert Fraser-Reid ... [et al.] --
Synthesis of N-5-derivatives of neuraminic acid and their software as sialosyl donors / Cristina De Meo --
2'-carboxybenzyl glycosides : a unique form of glycosyl donors and their software to oligosaccharide synthesis / Kwan Soo Kim and Heung Bae Jeon --
Oligosaccharide synthesis with glycosyl phosphates / Jeroen D.C. CodeĢe and Peter H. Seeberger --
Glycosyl thioimidates as flexible glycosyl donors for stereoselective O-glycosylation and convergent oligosaccharide synthesis / Papapida Pornsuriyasak, Medha N. Kamat, and Alexei V. Demchenko --
Sequential glycosylation innovations : a spotlight on thioglycosides as donors and acceptors / G.A. van der Marel ... [et al.] --
New apsects of glycoside bond formation : solid-phase oligosaccharide synthesis / Richard R. Schmidt, Simon Jonke, and Ke-gang Liu --
Synthesis of carbohydrate antigens on the topic of Shigella dysenteriae variety 1 and in their protein conjugates / Vince Pozsgay and Joanna Kubler-Kielb --
Enzymatic synthesis of glycosaminoglycans : bettering on nature / Fikri Y. Avci ... [et al.] --
The chemical synthesis of glycosylphosphatidylinositol anchors from Trypanosoma cruzi Trypomastigote mucins : exploration of ester and acetal variety everlasting keeping teams / Dmitry V. Yashunsky ... [et al.] --
Glycodiversification for the synthesis of neomycin and kanamycin classification aminoglycoside antiobiotics / Jinhua Wang and Cheng-Wei Tom Chang --
Convergent N-glycopeptide synthesis / Katja Michael --
concentrating on galectin-1 with self-assembled multivalent pseudopolyrotaxanes / Jason M. Belitsky and F. Fraser Stoddart --
De novo synthesis of biofunctional carbohydrate-encapsulated quantum dots / Sergei A. Svarosky and Joseph J. Barchi, Jr.

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Recently, we developed another synthetic pathway by enzymatic resolution of l-(2-furyl)ethanol followed by Achmatowicz rearrangement (Scheme 4) (14). In this pathway, furanaldehyde, an agrobased product, is used as starting material for preparation of the chiral a,p-unsaturated lactones. As an alternative way to construct the desired a,|3-unsaturated lactones, this strategy is more economic and more practical for large-scale manipulations than that one shown in scheme 2. So far, 20 uncommon sugars were obtained in large quantity (Figure 1) by using these two strategies in our group.

Tetrahedron Lett. 2002, 58, 6585-6594. Christner, D. ; Frank, B. ; Kozarich, J. ; Doyle, T. ; Rosenberg, I. ; Krishnan, B. J. Am. Chem. Soc. 1992, 114, 87638767. ; Pelyvas, I. F. ;Dekker: New York, 1994, 105-193. Pelyvas, I. ; Herczegh, P. ; Springer-Verlag: Berlin, 1988, 244pp. Cutchins, W. ; McDonald, F. E. Organic Lett. 2002, 4, 749-752. Nicolaou, K. ; Boddy, C. N . ; Winssinger, N . Angew. , Int. Ed. 1999, 38, 2096-2152. ; ACS Symposium Series; American Chemical Society: Washington, DC, 2007.

Matson, J. ; Forenza, S. Curr. Med. : Anti-cancer agents 2002, 2, 255-66. 28. ; Okamoto, K. ; Clardy, J. Tetrahedron Lett. 1985, 26, 4015-18. 29. ; Okanishi, M . J. Antibiot. 1991, 44, 723-8. 30. Nettleton, D. ; Doyle, T. ; Matsumoto, G. ; Clardy, J. Tetrahedron Lett. 1985, 26, 4011-14. ; ACS Symposium Series; American Chemical Society: Washington, DC, 2007. ch002 32 31. Arimondo, P. ; Helene, C. Curr. Med. : Anti-Cancer Agents 2001, 1, 219-235. 32. ; Waring, M . J. Mol. Pharmaco. 1998, 53, 77-87.

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