1 C alkyl disaccharides; 1 C alkyl hexopyranoses; Methyl 1 C methyl hexopyranosides; O glycosidation; O transglycosidation
Indexed keywords
1' C METHYL ALPHA O DISACCHARIDE DERIVATIVE;
2,3,4,6 TETRA O BENZYL 1 C METHYL ALPHA DEXTRO GALACTOPYRANOSE;
2,3,4,6 TETRA O BENZYL 1 C METHYL ALPHA DEXTRO GLUCOPYRANOSE;
2,3,4,6 TETRA O BENZYL 1 C METHYL ALPHA DEXTRO MANNOPYRANOSE;
2,3,4,6 TETRA O BENZYL 1 C VINYL ALPHA DEXTRO GALACTOPYRANOSE;
2,3,4,6 TETRA O BENZYL 1 C VINYL ALPHA DEXTRO GLUCOPYRANOSE;
2,3,4,6 TETRA O BENZYL 1 C VINYL ALPHA DEXTRO MANNOPYRANOSE;
CARBOHYDRATE DERIVATIVE;
GLUCOPYRANOSIDE;
METHYL 1 C METHYL HEXOPYRANOSIDE DERIVATIVE;
METHYL 2,3,4 TRI O BENZYL ALPHA DEXTRO GLUCOPYRANOSIDE;
METHYL 2,3,4,6 TETRA O BENZYL 1 C METHYL ALPHA DEXTRO GALACTOPYRANOSIDE;
METHYL 2,3,4,6 TETRA O BENZYL 1 C METHYL ALPHA DEXTRO GLUCOPYRANOSIDE;
METHYL 2,3,4,6 TETRA O BENZYL 1 C METHYL ALPHA DEXTRO MANNOPYRANOSIDE;
METHYL O (2',3',4',6' TETRA O ACETYL 1' C METHYL ALPHA DEXTRO GALACTOPYRANOSYL) (1'-6) 2,3,4 TRI O ACETYL ALPHA DEXTRO GLUCOSIDE;
METHYL O (2',3',4',6' TETRA O ACETYL 1' C METHYL ALPHA DEXTRO GLUCOPYRANOSYL) (1'-6) 2,3,4 TRI O ACETYL ALPHA DEXTRO GLUCOSIDE;
METHYL O (2',3',4',6' TETRA O ACETYL 1' C METHYL ALPHA DEXTRO MANNOPYRANOSYL) (1'-6) 2,3,4 TRI O ACETYL ALPHA DEXTRO GLUCOSIDE;
METHYL O (2',3',4',6' TETRA O BENZYL 1' C METHYL ALPHA DEXTRO GALACTOPYRANOSYL) (1'-6) 2,3,4 TRI O BENZYL ALPHA DEXTRO GLUCOSIDE;
METHYL O (2',3',4',6' TETRA O BENZYL 1' C METHYL ALPHA DEXTRO GLUCOPYRANOSYL) (1'-6) 2,3,4 TRI O BENZYL ALPHA DEXTRO GLUCOSIDE;
METHYL O (2',3',4',6' TETRA O BENZYL 1' C METHYL ALPHA DEXTRO MANNOPYRANOSYL) (1'-6) 2,3,4 TRI O BENZYL ALPHA DEXTRO GLUCOSIDE;
METHYL O (2',3',4',6' TETRA O BENZYL 1' C VINYL ALPHA DEXTRO GALACTOPYRANOSYL) (1'-6) 2,3,4 TRI O BENZYL ALPHA DEXTRO GLUCOSIDE;
METHYL O (2',3',4',6' TETRA O BENZYL 1' C VINYL ALPHA DEXTRO GLUCOPYRANOSYL) (1'-6) 2,3,4 TRI O BENZYL ALPHA DEXTRO GLUCOSIDE;
METHYL O (2',3',4',6' TETRA O BENZYL 1' C VINYL ALPHA DEXTRO MANNOPYRANOSYL) (1'-6) 2,3,4 TRI O BENZYL ALPHA DEXTRO GLUCOSIDE;
SUGAR ALCOHOL;
SULFONIC ACID DERIVATIVE;
TRIMETHYLSILYL TRIFLUOROMETHANE SULFONATE;
UNCLASSIFIED DRUG;
ANALYTIC METHOD;
ARTICLE;
CHEMICAL REACTION;
CHEMICAL STRUCTURE;
PRIORITY JOURNAL;
STEREOCHEMISTRY;
STRUCTURE ANALYSIS;
SYNTHESIS;
Anomeric-oxygen activation for glycoside synthesis: The trichloroacetimidate method
Horton D. San Diego: Academic Press
Schmidt R.R., Kinzy W. Anomeric-oxygen activation for glycoside synthesis: the trichloroacetimidate method. Horton D. Adv. Carbohydr. Chem. Biochem. Vol. 50:1994;21-123 Academic Press, San Diego.
Lederkremer R.M., Varela O. Synthetic reactions of aldonolactones. Horton D. Adv. Carbohydr. Chem. Biochem. Vol. 50:1994;125-209 Academic Press, San Diego.
Prepared from the corresponding 2,3,4,6-tetra-O-benzylhexopyranose by the oxidation with acetic anhydride and DMSO. see
Prepared from the corresponding 2,3,4,6-tetra-O-benzylpyranose by the oxidation with acetic anhydride and DMSO, see: Kuzuhara, H., Fletcher, Jr., H. G. J. Org. Chem. 1967, 32, 2531-2534.
The compounds 7a-c could also be prepared from the glycosidations of the corresponding 1-methylenesugars and methanol under the catalysis of TfOH (0.1 equiv.) following the procedure in Ref. 11
The compounds 7a-c could also be prepared from the glycosidations of the corresponding 1-methylenesugars and methanol under the catalysis of TfOH (0.1 equiv.) following the procedure in Ref. 11.
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0003463148
Eds., John Wiley and Sons, Inc.: New York
Greene, T. W.; Wuts, P. G. M.; Eds., Protective Groups in Organic Synthesis; 2nd Ed., John Wiley and Sons, Inc.: New York, 1991; pp. 14-17.
Chemistry, metabolism, and biological functions of sialic acids
R.S. Tipson, Horton D. New York: Academic Press
Schauer R. Chemistry, metabolism, and biological functions of sialic acids. Tipson R.S., Horton D. Adv. Carbohydr. Chem. Biochem. Vol. 40:1982;132-234 Academic Press, New York.