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0022636075
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New methods for the synthesis of glycosides oligosaccharides - Are there alternatives to the Koenigs-Knorr method?
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Schmidt, R.R. New methods for the synthesis of glycosides oligosaccharides - Are there alternatives to the Koenigs-Knorr method? Angew. Chem. Int. Ed. Engl. 1986, 25, 212-235.
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Angew. Chem. Int. Ed. Engl
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Schmidt, R.R.1
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2
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0028186224
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Anomeric oxygen activation for glycoside synthesis. The trichloroacetimidate method
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Schmidt, R.R.; Kinzy, W. Anomeric oxygen activation for glycoside synthesis. The trichloroacetimidate method. Adv. Carbohydr. Chem. Biochem. 1994, 50, 21-123.
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Adv. Carbohydr. Chem. Biochem
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Schmidt, R.R.1
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3
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84956517326
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Ernst, B, Hart, G.W, Sinaÿ, P, Eds, Wiley-VCH: Weinheim
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Schmidt, R.R.; Jung, K.-H. Trichloroacetimidates. In Carbohydrates in Chemistry and Biology, Part I: Chemistry of Saccharides; Ernst, B., Hart, G.W., Sinaÿ, P., Eds.; Wiley-VCH: Weinheim, 2000; Vol. 1, 5-59.
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Carbohydrates in Chemistry and Biology, Part I: Chemistry of Saccharides
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Schmidt, R.R.1
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4
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5244279498
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Recent progress in O-glycosylation methods and its application to natural products synthesis
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Toshima, K.; Tatsuta, K. Recent progress in O-glycosylation methods and its application to natural products synthesis. Chem. Rev. 1993, 93, 1503-1531.
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Chem. Rev
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Toshima, K.1
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6
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0001513404
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Einfache Synthese von α- und β-O-Glycosylimidaten. Herstellung von Glykosiden und Disacchariden
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Schmidt, R.R.; Michel, J. Einfache Synthese von α- und β-O-Glycosylimidaten. Herstellung von Glykosiden und Disacchariden. Angew. Chem. Int. Ed. Engl. 1980, 92, 763-764.
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Schmidt, R.R.1
Michel, J.2
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7
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34547361380
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Dissertation, Universität Konstanz, Verlag Papierflieger, Clausthal-Zellerfeld: New York
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Huchel, U. Neue Methoden zur diastereoselektiven Glycosylierung. Dissertation, Universität Konstanz, Verlag Papierflieger, Clausthal-Zellerfeld: New York, 1998.
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Neue Methoden zur diastereoselektiven Glycosylierung
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Huchel, U.1
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8
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0035906067
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Glycosyl trifluoroacetimidates. Part 1: Preparation and application as new glycosyl donors
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Yu, B.; Tao, H. Glycosyl trifluoroacetimidates. Part 1: preparation and application as new glycosyl donors. Tetrahedron Lett. 2001, 42, 2405-2408.
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Yu, B.1
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0037073937
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Glycosyl trifluoroacetimidates. 2. Synthesis of dioscin and xiebai saponin I
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Yu, B.; Tao, H. Glycosyl trifluoroacetimidates. 2. Synthesis of dioscin and xiebai saponin I. J. Org. Chem. 2002, 67, 9099-9102.
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Yu, B.1
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0036166613
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Iodine/Triethylsilane as a convenient promoter system for the activation of disarmed glycosyl trichloro- and N-(phenyl)trifluoroacetimidates
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Adinolfi, M.; Barone, G.; Iademisi, A.; Schiattarella, M. Iodine/Triethylsilane as a convenient promoter system for the activation of disarmed glycosyl trichloro- and N-(phenyl)trifluoroacetimidates. Synlett 2002, 269-272.
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Adinolfi, M.1
Barone, G.2
Iademisi, A.3
Schiattarella, M.4
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11
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0029560621
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Direct anomeric O-arylation and O-hetary-lation of glucose -electron deficient aromatic and heteroaromatic compounds in aryl and hetaryl glycoside synthesis
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Huchel, U.; Schmidt, C.; Schmidt, R.R. Direct anomeric O-arylation and O-hetary-lation of glucose -electron deficient aromatic and heteroaromatic compounds in aryl and hetaryl glycoside synthesis. Tetrahedron Lett. 1995, 36, 9457-9460.
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Tetrahedron Lett
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Huchel, U.; Schmidt, C.; Schmidt, R.R. Synthesis of hetaryl glycosides and their glycosyl donor properties. Eur. J. Org. Chem. 1998, 1353-1360; and references therein.
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Huchel, U.; Schmidt, C.; Schmidt, R.R. Synthesis of hetaryl glycosides and their glycosyl donor properties. Eur. J. Org. Chem. 1998, 1353-1360; and references therein.
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13
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0029154238
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The stereocontrolled synthesis of 1,2-cis furanosyl nucleosides via a novel anomeric activation
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Hanessian, S.; Condé, J.J.; Lion, B. The stereocontrolled synthesis of 1,2-cis furanosyl nucleosides via a novel anomeric activation. Tetrahedron Lett. 1995, 36, 5865-5868.
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Hanessian, S, Ed, Marcel Dekker Inc: New York, references therein
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Preparative Carbohydrate Chemistry
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0000991908
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2,3,4,6-Tetra-O-benzyl-α-D- glucopyranose
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Whistler, R.L, BeMiller, J.N, Eds, Academic Press: New York
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Glaudemans, P.J.; Fletcher, H.G., Jr. 2,3,4,6-Tetra-O-benzyl-α-D- glucopyranose. In Methods in Carbohydrate Chemistry; Whistler, R.L., BeMiller, J.N., Eds.; Academic Press: New York, 1972; Vol. VI, 373-376.
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Fletcher Jr., H.G.2
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The allyl ether as a protecting group in carbohydrate chemistry
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49549143786
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Coupure sélective par l'hydrazine des groupements acétyles anomères de résidus glycosyles acetyls
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Excoffier, G.; Gagnaire, D.; Utille, J.P. Coupure sélective par l'hydrazine des groupements acétyles anomères de résidus glycosyles acetyls. Carbohydr. Res. 1975, 39, 368-373.
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19
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34547273476
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Compound 3a is commercially available
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Compound 3a is commercially available.
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20
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0017287872
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Dehydrogenation of the phosphonate analogue of glucose 6-phosphate by glucose 6-phosphate dehydrogenase
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For compound 3b see
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For compound 3b see: Adams, P.R.; Harrison, R.; Inch, T.D.; Rich, P. Dehydrogenation of the phosphonate analogue of glucose 6-phosphate by glucose 6-phosphate dehydrogenase. Biochem. J. 1976, 155, 1-4.
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Adams, P.R.1
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Inch, T.D.3
Rich, P.4
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21
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0002086064
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A novel reductive ring-opening of carbohydrate benzylidene acetals
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For compound 3c see: Garegg, P. J.; Hultberg, H.; Wallin, S. A novel reductive ring-opening of carbohydrate benzylidene acetals. Carbohydr. Res. 1982, 108, 97-101.
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Hultberg, H.2
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22
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0001205939
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Isopropylidene derivatives
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For compound 3d see:, Whistler, R.L, Wolfram, L, Eds, Academic Press: New York
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For compound 3d see: Schmidt, O.T. Isopropylidene derivatives. In Methods in Carbohydrate Chemistry; Whistler, R.L., Wolfram, L., Eds.; Academic Press: New York, 1963; Vol. II, 320-321.
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Schmidt, O.T.1
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33751157840
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Glycosyl phosphites as glycosylation reagents: Scope and mechanism
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Kondo, H.; Aoki, S.; Ichikawa, Y.; Halcomb, R.L.; Ritzen, H.; Wong, C.H. Glycosyl phosphites as glycosylation reagents: scope and mechanism. J. Org. Chem. 1994, 59, 864-877.
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Wong, C.H.6
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25
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0017785167
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A novel synthesis of 1,2-czs-disaccharides
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Sinaÿ, P.; Pougny, J.R.; Jacquinet, J.C.; Nassr, M.; Duchet, D. A novel synthesis of 1,2-czs-disaccharides. J. Am. Chem. Soc. 1977, 99, 6762-6763.
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Duchet, D.5
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26
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0001389242
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O-(α-D-Glucopyranosyl)- trichloracetimidate as glycosyl donor
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Schmidt, R.R.; Michel, J. O-(α-D-Glucopyranosyl)- trichloracetimidate as glycosyl donor. J. Carbohydr. Chem. 1985, 4, 141-169.
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J. Carbohydr. Chem
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84988126671
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Nitriles as solvents in glycosylation reactions - highly selective β-glycoside synthesis
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Schmidt, R.R.; Behrendt, M.; Töpfer, A. Nitriles as solvents in glycosylation reactions - highly selective β-glycoside synthesis. Synlett 1990, 694-697.
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28
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0001067482
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The application of the trichloroacetimidate method to the synthesis of α-D-gluco- and α-D-galactopyranosides
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Wegmann, B.; Schmidt, R.R. The application of the trichloroacetimidate method to the synthesis of α-D-gluco- and α-D-galactopyranosides. J. Carbohydr. Chem. 1987, 6, 357-375.
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J. Carbohydr. Chem
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0029882333
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Glycosamino acids: New building blocks for combinatorial synthesis
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McDevitt, J.P.; Lansbury, P.T., Jr. Glycosamino acids: new building blocks for combinatorial synthesis. J. Am. Chem. Soc. 1996, 118, 3818-3828.
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McDevitt, J.P.1
Lansbury Jr., P.T.2
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