104845-98-9

Upstream product

• 2862-10-4 benzyl-(2-benzyloxycarbonylamino-2-deoxy-α-D-glucopyranoside) 
• 106455-74-7 Benzyl-3,4-di-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-6-O--α-D-glucopyranosid 
• 106434-48-4 ((2S,3R,4R,5S,6R)-2,4,5-Tris-benzyloxy-6-trityloxymethyl-tetrahydro-pyran-3-yl)-carbamic acid benzyl ester 
• 106434-47-3 Benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-6-O-(triphenylmethyl)-α-D-glucopyranosid 
• 100-39-0 benzyl bromide 
• 85382-87-2 methyl (4,5,7,8-tetra-O-acetyl-3-deoxy-α-D-manno-oct-2-ulopyranosyl bromide)onate 
• 57690-71-8 Benzyl-3,4-di-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-α-D-glucopyranosid 
• 104845-96-7 Benzyl-3,4-di-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-6-O--α-D-glucopyranosid 
• 104845-95-6 (2R,4R,5R,6R)-6-((S)-1,2-Dihydroxy-ethyl)-4,5-dihydroxy-2-((2R,3S,4R,5R,6S)-3,4,6-tris-benzyloxy-5-benzyloxycarbonylamino-tetrahydro-pyran-2-ylmethoxy)-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 148152-74-3 methyl (4,5,7,8-tetra-O-acetyl-3-deoxy-α-D-manno-2-octulopyranosyl bromide)onate 
• 104845-96-7 (2R,4R,5R,6S)-6-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-4,5-dihydroxy-2-((2R,3S,4R,5R,6S)-3,4,6-tris-benzyloxy-5-benzyloxycarbonylamino-tetrahydro-pyran-2-ylmethoxy)-tetrahydro-pyran-2-carboxylic acid methyl ester 

Downstream Products

• 104846-12-0 Benzyl-O--(2->4)-O--(2->6)-3,4-di-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-α-D-glucopyranosid 
• 104846-13-1 Benzyl-O-<(3-desoxy-α-D-manno-2-octulopyranosyl)onsaeure>-(2->4)-O-<(3-desoxy-α-D-manno-2-octulopyranosyl)onsaeure>-(2->6)-3,4-di-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-α-D-glucopyranosid 
• 106434-57-5 C₅₂H₆₁NO₂₀ 
• 104846-11-9 Benzyl-O--(2->4)-O--(2->6)-3,4-di-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-α-D-glucopyranosid 
• 104846-13-1 C₅₁H₆₁NO₂₁ 
• 104846-11-9 C₆₁H₇₃NO₂₅ 

Relevant academic research and scientific papers

Building Units of Oligosaccharides, LXXIX. - Synthesis of the Sequence α-KDO-(2-->4)-α-KDO-(2-->6)-D-GlcN of the "Inner Core" Structure of Lipopolysaccharides

The glycosyl halide of 3-deoxy-D-manno-2-octulosonic acid (KDO) (5) reacts with the D-glucosamine derivative 4 to give the α-(2-->6) glycosidically linked disaccharide 6.After deacetylation from 6 to 7 and conversion into the isopropylidene sugar 16, the

SYNTHESE EINES 3-DESOXY-D-MANNO-2-OCTULOSONSAEURE(KDO)-HALTIGEN TETRASACCHARIDES UND DESSEN STRUKTURVERGLEICH MIT EINEM ABBAU-PRODUKT AUS BAKTERIEN-LIPOPOLYSACCHARIDEN

The tetrasaccharide α-KDO-(2-4)-α-KDO-(2-6)-β-D-GlcN(1-6)-D-GlcN 18 has been synthesized in a sequencial oligosaccharide synthesis.This compound is identical with the degradation product which has been isolated from a R-mutant of Salmonella minnesota.Thus