29024-87-1

Upstream product

• 100-39-0 benzyl bromide 
• 43168-73-6 methyl 2,3-anhydro-β-D-lyxofuranoside 
• 51754-99-5 Methyl 3,5-O-Isopropylidene-β-D-xylofuranoside 
• 551929-54-5 methyl-[O³,O⁵-isopropylidene-O²-(toluene-4-sulfonyl)-β-D-xylofuranoside] 
• 1009818-08-9 (2R,3R,4R)-2-((benzyloxy)methyl)-5-methoxytetrahydrofuran-3,4-diol 

Downstream Products

• 28867-47-2 methyl 5-O-benzyl-3-fluoro-3-deoxy-β-D-arabino-furanoside 
• 138147-45-2 methyl 5-O-benzyl-2-deoxy-β-D-threo-pentofuranoside 
• 133776-22-4 Benzoic acid (2R,3S,4S,5S)-5-(2-acetylamino-6-oxo-1,6-dihydro-purin-7-yl)-4-azido-3-fluoro-tetrahydro-furan-2-ylmethyl ester 
• 133776-34-8 Benzoic acid (2R,3S,4S,5R)-5-(2-acetylamino-6-oxo-1,6-dihydro-purin-7-yl)-4-azido-3-fluoro-tetrahydro-furan-2-ylmethyl ester 
• 133776-20-2 Benzoic acid (2R,3S,4S,5S)-4-azido-5-(6-benzoylamino-purin-9-yl)-3-fluoro-tetrahydro-furan-2-ylmethyl ester 
• 133776-32-6 Benzoic acid (2R,3S,4S,5R)-4-azido-5-(6-benzoylamino-purin-9-yl)-3-fluoro-tetrahydro-furan-2-ylmethyl ester 
• 133776-21-3 Benzoic acid (2R,3S,4S,5S)-5-(2-acetylamino-6-oxo-1,6-dihydro-purin-9-yl)-4-azido-3-fluoro-tetrahydro-furan-2-ylmethyl ester 
• 133776-33-7 Benzoic acid (2R,3S,4S,5R)-5-(2-acetylamino-6-oxo-1,6-dihydro-purin-9-yl)-4-azido-3-fluoro-tetrahydro-furan-2-ylmethyl ester 
• 126716-24-3 methyl 5-O-benzyl-2-O-tosyl-3-fluoro-3-deoxy-β-D-arabino-furanoside 
• 123484-12-8 ((2R,3R,4S)-5-acetoxy-4-(benzoyloxy)-3-fluorotetrahydrofuran-2-yl)methyl benzoate 
• 112695-36-0 methyl 2,5-di-O-benzoyl-3-fluoro-3-deoxy-β-D-ribofuranoside 
• 124939-88-4 methyl 5-O-benzyl-2-O-benzoyl-3-fluoro-3-deoxy-β-D-ribofuranoside 
• 133776-11-1 2-azido-5-O-benzoyl-2,3-dideoxy-3-fluoro-α-D-ribofuranoside 
• 133776-29-1 2-azido-5-O-benzoyl-3-fluoro-2,3-dideoxy-β-D-ribofuranoside 

Relevant academic research and scientific papers

Probing the catalytic mechanism of s-ribosylhomocysteinase (LuxS) with catalytic intermediates and substrate analogues

S-Ribosylhomocysteinase (LuxS) cleaves the thioether bond in S-ribosylhomocysteine (SRH) to produce homocysteine (Hcys) and 4,5-dihydroxy-2,3-pentanedione (DPD), the precursor of the type II bacterial quorum sensing molecule (AI-2). The catalytic mechanis

Synthesis and antiviral and cytostatic properties of 3'-deoxy-3'-fluoro- and 2'-azido-3'-fluoro-2',3'-dideoxy-D-ribofuranosides of natural heterocyclic bases

A series of 3'-deoxy-3'-fluoro- and 2'-azido-2',3'-dideoxy-3'-fluoro-D-ribofuranosides of natural heterocyclic bases have been synthesized with the use of universal carbohydrate precursors, viz., 1-O-acetyl-2,5-di-O-benzoyl-3-deoxy-3-fluoro-D-ribofuranose