64609-17-2

Upstream product

• 103702-71-2 benzyl 2,3,5-tri-O-benzoyl-α-D-arabinofuranoside 
• 100-51-6 benzyl alcohol 
• 4348-68-9 2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl bromide 
• 64609-16-1 benzyl 2,3,5-tri-O-acetyl-α-D-arabinofuranoside 

Downstream Products

• 103702-73-4 C₃₁H₃₀O₅ 
• 1579197-75-3 methyl (benzyl (Z)-2,3-di-O-triisopropylsilyl-5-O-methyl-a-D-altro-hex-4-enofuranosid)uronate 
• 1579197-73-1 C₃₂H₅₆O₇Si₂ 
• 1046825-04-0 benzyl-5-O-acetyl-α-D-arabinofuranoside 
• 878288-87-0 benzyl 2-O-benzyl-5-deoxy-5-[2,3,5-tri-O-benzyl-1,4-dideoxy-1,4-episulfoniumylidene-D-arabinitol]-3-O-sulfoxy-α-D-arabinofuranose inner salt 
• 878288-83-6 benzyl 2-O-benzyl-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-α-D-arabinofuranoside 
• 878288-81-4 benzyl 2-O-benzyl-α-D-arabinofuranoside-3,5-cyclic sulfide 
• 878288-79-0 benzyl 2-O-benzyl-α-D-arabinofuranoside 

Relevant academic research and scientific papers

An unexpected rearrangement of pent-4-enofuranosides to cyclopentanones upon hydrogenolysis of the anomeric benzyl group

During our synthesis toward the unique nucleoside antibiotic A201A, we were surprised to find that a benzyl arabino-pent-4-enofuranoside underwent a Ferrier II-like rearrangement readily to provide the corresponding cyclopentanone derivative in high yield and stereoselectivity upon hydrogenolysis of the anomeric benzyl group.

A simple synthesis of C-8 modified 2-keto-3-deoxy-d-manno-octulosonic acid (KDO) derivatives

This paper describes a simple and efficient method with which to prepare C-8 modified 2-keto-3-deoxy-D-manno-octu-losonic acid (KDO) derivatives from C-5 modified arabinose derivatives. Georg Thieme Verlag Stuttgart.

Synthesis of sulfonium sulfate analogues of disaccharides and their conversion to chain-extended homologues of salacinol: New glycosidase inhibitors

Four chain extended homologues of salacinol, a naturally occurring glycosidase inhibitor, were prepared for evaluation as inhibitors of glucosidase enzymes involved in the breakdown of carbohydrates. The syntheses involved the reactions of 1,4-anhydro-2,3