ORTHOGONAL GLYCOSYLATION STRATEGY IN OLIGOSACCHARIDE SYNTHESIS

[11] IODONIUM PROMOTED REACTIONS OF DISARMED THIOGLYCOSIDES [J]. TETRAHEDRON LETTERS, 1990, 31 (30) : 4313 - 4316

[12] IODONIUM ION GENERATED INSITU FROM N-IODOSUCCINIMIDE AND TRIFLUOROMETHANESULFONIC ACID PROMOTES DIRECT LINKAGE OF DISARMED PENT-4-ENYL GLYCOSIDES [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1990, (03) : 270 - 272

[13] STEREOCONTROLLED SYNTHESIS OF CHITOSAN DODECAMER [J]. CARBOHYDRATE RESEARCH, 1993, 243 (01) : C1 - C7

[14] HUMAN-BLOOD GROUPS AND CARBOHYDRATE-CHEMISTRY [J]. CHEMICAL SOCIETY REVIEWS, 1978, 7 (04) : 423 - 452

[15] LEMIEUX RU, 1976, ACS SYM SER, V4, P90

[16] SYNTHESIS OF A TRI-SACCHARIDE AND A HEPTA-SACCHARIDE WHICH CONTAIN ALPHA-L-FUCOPYRANOSYL GROUPS AND ARE PART OF THE COMPLEX TYPE OF CARBOHYDRATE MOIETY OF GLYCOPROTEINS [J]. CARBOHYDRATE RESEARCH, 1985, 139 (JUN) : 105 - 113

[17] A NOVEL CLASS OF GLYCOSYL DONORS - ANOMERIC S-XANTHATES OF 2-AZIDO-2-DEOXY-D-GALACTOPYRANOSYL DERIVATIVES [J]. TETRAHEDRON, 1991, 47 (28) : 5149 - 5160

[18] ISOPROPENYL GLYCOSIDES AND CONGENERS AS NOVEL CLASSES OF GLYCOSYL DONORS - THEME AND VARIATIONS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (16) : 6354 - 6360

[19] PHENYLSELENOGLYCOSIDES AS NOVEL, VERSATILE GLYCOSYL DONORS - SELECTIVE ACTIVATION OVER THIOGLYCOSIDES [J]. TETRAHEDRON LETTERS, 1991, 32 (35) : 4435 - 4438

[20] NOVEL GLYCOSIDATION METHODOLOGY - THE USE OF PHENYL SELENOGLYCOSIDES AS GLYCOSYL DONORS AND ACCEPTORS IN OLIGOSACCHARIDE SYNTHESIS [J]. JOURNAL OF ORGANIC CHEMISTRY, 1993, 58 (12) : 3269 - 3276

[11] IODONIUM PROMOTED REACTIONS OF DISARMED THIOGLYCOSIDES [J]. TETRAHEDRON LETTERS, 1990, 31 (30) : 4313 - 4316

[12] IODONIUM ION GENERATED INSITU FROM N-IODOSUCCINIMIDE AND TRIFLUOROMETHANESULFONIC ACID PROMOTES DIRECT LINKAGE OF DISARMED PENT-4-ENYL GLYCOSIDES [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1990, (03) : 270 - 272

[13] STEREOCONTROLLED SYNTHESIS OF CHITOSAN DODECAMER [J]. CARBOHYDRATE RESEARCH, 1993, 243 (01) : C1 - C7

[14] HUMAN-BLOOD GROUPS AND CARBOHYDRATE-CHEMISTRY [J]. CHEMICAL SOCIETY REVIEWS, 1978, 7 (04) : 423 - 452

[15] LEMIEUX RU, 1976, ACS SYM SER, V4, P90

[16] SYNTHESIS OF A TRI-SACCHARIDE AND A HEPTA-SACCHARIDE WHICH CONTAIN ALPHA-L-FUCOPYRANOSYL GROUPS AND ARE PART OF THE COMPLEX TYPE OF CARBOHYDRATE MOIETY OF GLYCOPROTEINS [J]. CARBOHYDRATE RESEARCH, 1985, 139 (JUN) : 105 - 113

[17] A NOVEL CLASS OF GLYCOSYL DONORS - ANOMERIC S-XANTHATES OF 2-AZIDO-2-DEOXY-D-GALACTOPYRANOSYL DERIVATIVES [J]. TETRAHEDRON, 1991, 47 (28) : 5149 - 5160

[18] ISOPROPENYL GLYCOSIDES AND CONGENERS AS NOVEL CLASSES OF GLYCOSYL DONORS - THEME AND VARIATIONS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (16) : 6354 - 6360

[19] PHENYLSELENOGLYCOSIDES AS NOVEL, VERSATILE GLYCOSYL DONORS - SELECTIVE ACTIVATION OVER THIOGLYCOSIDES [J]. TETRAHEDRON LETTERS, 1991, 32 (35) : 4435 - 4438

[20] NOVEL GLYCOSIDATION METHODOLOGY - THE USE OF PHENYL SELENOGLYCOSIDES AS GLYCOSYL DONORS AND ACCEPTORS IN OLIGOSACCHARIDE SYNTHESIS [J]. JOURNAL OF ORGANIC CHEMISTRY, 1993, 58 (12) : 3269 - 3276