186087-86-5

Upstream product

• 140397-49-5 (2S,3S,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-carbaldehyde 
• 207797-38-4 C₃₆H₃₈O₇ 
• 3866-62-4 1-O-acetyl-2,3,4,6-tetra-O-benzyl-D-mannopyranose 
• 4132-28-9 2,3,4,6-tetra-O-benzyl-D-mannopyranose 
• 188819-43-4 (2R,3R,4R,5R,6R)-3,4,5-tribenzyloxy-6-(benzyloxymethyl)tetrahydropyran-2-carbonitrile 
• 194980-06-8 (2R,3R,4R,5R,6R)-3,4,5-tris(benzyloxy)-2-(benzyloxymethyl)-6-((E)-prop-1-enyl)tetrahydro-2H-pyran 
• 82659-59-4 3-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)propene 
• 124-38-9 carbon dioxide 
• 186087-99-0 diphenyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside phosphate 

Downstream Products

• 1063748-00-4 methyl 2,3,4-tri-O-benzyl-6-O-[(N-2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)carbamoyl]-α-D-glucopyranoside 
• 207387-07-3 {(2S,4aR,6R,7S,8R,8aR)-6-Methoxy-2-phenyl-7-[((2S,3S,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-carbonyl)-amino]-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy}-acetic acid 

Relevant academic research and scientific papers

A general approach to C-Acyl glycosides via palladium/copper Co-catalyzed coupling reaction of glycosyl carbothioates and arylboronic acids

A general and efficient approach to the synthesis of various C-acyl glycosides has been developed via Pd2(dba)3/CuTC co-catalyzed cross-coupling reaction of glycosyl carbothioates with arylboronic acids. The reaction showed a broad s

Novel synthesis of oligosaccharides linked with carbamate and urea bonds utilizing modified Curtius rearrangement

We describe a novel synthesis of various carbamate- and urea-linked disaccharides stereospecifically using sugar carboxylic acids and sugar alcohols or sugar amines by the modified Curtius rearrangement. In this reaction, the reactivity of each hydroxyl g

Small molecules as structural and functional mimics of sialyl Lewis X tetrasaccharide in selectin inhibition: A remarkable enhancement of inhibition by additional negative charge and/or hydrophobic group

Several sialyl Lewis X (SLe(X))) mimics that contain the essential functional groups for receptor interaction and a negative charge or a hydrophobic group have been developed as inhibitors of E-, P-, and L-selectins. Some of the mimics exhibit selectin in

Samariumdiiodid-vermittelte Kupplung von Glycosylphosphaten mit Kohlenstoffradikal- oder -anion-Acceptoren - Synthese von C-Glycosiden

Keywords: C-Glycoside; Verknuepfungen; Samariumverbindungen; Synthesemethoden