488719-74-0

Upstream product

• 327593-88-4 allyl 2-O-benzyl-α-L-fucopyranoside 

Downstream Products

• 582322-37-0 allyl 3-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl-(1->3)-2-O-benzyl-α-L-fucopyranosyl-(1->3)-2-O-benzyl-α-L-fucopyranoside 
• 582322-36-9 allyl 2-O-benzyl-α-L-fucopyranosyl-(1->3)-2-O-benzyl-α-L-fucopyranosyl-(1->3)-2-O-benzyl-α-L-fucopyranoside 
• 582322-35-8 allyl 3,4-di-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl-(1->3)-2-O-benzyl-α-L-fucopyranosyl-(1->3)-2-O-benzyl-α-L-fucopyranoside 
• 488719-75-1 allyl 3-O-(3-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl)-2-O-benzyl-α-L-fucopyranoside 

Relevant academic research and scientific papers

Synthesis of the oligosaccharides related to branching sites of fucosylated chondroitin sulfates from sea cucumbers

Natural anionic polysaccharides fucosylated chondroitin sulfates (FCS) from sea cucumbers attract great attention nowadays due to their ability to influence various biological processes, such as blood coagulation, thrombosis, angiogenesis, inflammation, b

Synthesis, NMR, and conformational studies of fucoidan fragments. IV.[1] 4-Mono- and 4,4′-disulfated (1→3)-α-l-fucobioside and 4-sulfated fucoside fragments

Propyl 4-O-sulfonato- and 4,4′-di-O-sulfonato-3-O-α-L-fucopyranosyl-α-L- fucopyranosides, which are related to fragments of brown algal fucoidans, have been synthesized. Their spectral (1H and 13C NMR, NOE) and conformational propert