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3042758507
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The benzylidene acetal fragmentation route to 6-deoxy sugars: Direct reductive cleavage in the presence of ether protecting groups permitting the efficient, highly stereocontrolled synthesis of β-D-rhamnosides from D-mannosyl glycosyl donors. Total synthesis of α-D-Gal-(1 → 3)-α-D-Rha-(1 → 3)-β-D-Rha-(1 → 4)-β-D-Glu-OMe
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the repeating unit of the antigenic lipopolysaccharide from Escherichia hermannii ATCC 33650 and 33652
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Crich, D.; Yao, Q. The benzylidene acetal fragmentation route to 6-deoxy sugars: direct reductive cleavage in the presence of ether protecting groups permitting the efficient, highly stereocontrolled synthesis of β-D-rhamnosides from D-mannosyl glycosyl donors. Total synthesis of α-D-Gal-(1 → 3)-α-D-Rha-(1 → 3)-β-D-Rha)-(1 → 4)-β-D-Glu-OMe, the repeating unit of the antigenic lipopolysaccharide from Escherichia hermannii ATCC 33650 and 33652. J. Am. Chem. Soc. 2004, 126, 8232-8236.
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10044253272
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11
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0037427286
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2,3-Anhydro sugars in glycoside bond synthesis. Highly stereoselective syntheses of oligosaccharides containing α- and β-arabinofuranosyl linkages
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Gadikota, R.R.; Callam, C.S.; Wagner, T.; Del Fraino, B.; Lowary, T.L. 2,3-Anhydro sugars in glycoside bond synthesis. Highly stereoselective syntheses of oligosaccharides containing α- and β-arabinofuranosyl linkages. J. Am. Chem. Soc. 2003, 125, 4155-4165.
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0004479651
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p-Toluenesulfinyl chloride
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0036187765
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0032537702
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-
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0035122651
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2,4,6-Tri-tert-butylpyrimidine (TTBP): A cost effective, readily available alternative to the hindered base 2,6-di-tert-butylpyridine and its 4-substituted derivatives in glycosylation and other reactions
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0042853252
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Codée, J.D.C.; van den Bos, J.; Litjens, R.E.J.N.; Overkleeft, H.S.; van Boom, J.H.; van der Marel, G.A. Sequential one-pot glycosylations using 1-hydroxy and 1-thiodonors. Org. Lett. 2003, 5, 1947-1950.
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Van Der Marel, G.A.6
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24
-
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13844320100
-
6-O-Benzyl and 6-O-silyl-N-acetyl-2-amino-2N,3-O-carbonyl-2- deoxyglucosides: Effective glycosyl acceptors in the glucosamine 4-OH series. Effect of anomeric stereochemistry on the removal of the oxazolidinone group
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Crich, D.; Vinod, A.U. 6-O-Benzyl and 6-O-silyl-N-acetyl-2-amino-2N,3-O- carbonyl-2-deoxyglucosides: Effective glycosyl acceptors in the glucosamine 4-OH series. Effect of anomeric stereochemistry on the removal of the oxazolidinone group. J. Org. Chem. 2005, 70, 1291-1296.
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0142026534
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26
-
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12344274639
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Disarming, non-participating 2-O-protecting groups in manno- And rhamnopyranosylation: Scope and limitations of sulfonates, vinylogous esters, phosphates, cyanates, and nitrates
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-
27
-
-
27844515435
-
-
note
-
The differing polarity of the byproducts from the sulfinamide method and the diphenyl sulfoxide methods is an advantage, and it is sometimes found that switching from one of these activating systems to the other can greatly facilitate purification.
-
-
-
-
28
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1642357409
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N-(Phenylthio)-ε-caprolactam: A new promoter for the activation of thioglycosides
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0000505349
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0000275934
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34
-
-
27844545621
-
-
note
-
1 for this compound. The correct data are given here.
-
-
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