878384-17-9

Upstream product

• 878384-14-6 1,4-anhydro-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-4-thio-D-arabinitol 
• 878384-15-7 1,4-anhydro-2-deoxy-2-fluoro-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-4-thio-D-arabinitol 
• 878384-22-6 1,4-anhydro-2-deoxy-2-fluoro-4-thio-D-arabinitol 
• 98-88-4 benzoyl chloride 
• 401817-76-3 5-O-benzyl-2,3-O-isopropylidene-L-lyxono-1,4-lactone 
• 1311428-43-9 1,4-anhydro-5-O-benzyl-2,3-O-sulphonyl-4-thio-D-ribitol 
• 1311428-40-6 1,4-Anhydro-5-O-benzyl-4-thio-D-ribitol 
• 1311428-45-1 1,4-anhydro-5-O-benzyl-2-deoxy-2-fluoro-4-thio-D-arabinitol 
• 1311428-39-3 1,4-anhydro-5-O-benzyl-2,3-O-isopropylidene-4-thio-D-ribitol 
• 1311428-37-1 1-O-benzyl-3,4-O-isopropylidene-2,5-di-O-methanesulphonyl-L-arabinitol 
• 1311428-36-0 1-O-benzyl-3,4-O-isopropylidene-L-arabinitol 
• 160882-26-8 (2R,3S,4S)-2-(hydroxymethyl)tetrahydrothiophene-3,4-diol 

Downstream Products

• 878384-20-4 (2S,3S,4S)-2-acetoxy-3-benzoyloxy-2-benzoyloxymethyl-4-fluorotetrahydrothiophene 
• 878384-18-0 1,4-anhydro-2-deoxy-2-fluoro-3,5-di-O-benzoyl-4-sulfinyl-D-arabinitol 

Relevant academic research and scientific papers

PROCESS FOR PREPARING SUBSTITUTED 1-O-ACYL-2-DEOXY-2-FLUORO-4-THIO-β-D-ARABINOFURANOSES

The present invention relates to a process for preparing 1-O-acyl-2-deoxy-2-fluoro-4-thio-??-D-arabinofuranoses having formula I and intermediates thereof: wherein R1 represents -C(O)-C1-C6-alkyl or -C(O)-aryl; and R2 represents C1-C6-alkyl, C1-C4-perfluo

PROCESS FOR PREPARING SUBSTITUTED 1-O-ACYL-2-DEOXY-2-FLUORO-4-THIO-BETA-D-ARABINOFURANOSES

The present invention relates to a process for preparing 1-O-acyl-2-deoxy-2-fluoro-4-thio-β-D-arabinofuranoses having formula I and intermediates thereof: wherein R1 represents —C(O)—C1-C6-alkyl or —C(O)-aryl; and R2

Process for preparing substituted 1-O-acyl-2-deoxy-2-fluoro-4-thio-?-D-arabinofuranoses

The present invention relates to a process for preparing 1-0-acyl-2-deoxy-2-fluoro-4-thio-β-D-arabinofuranoses in which R1 represents C(O)-C1-C6-alkyl or C(O)-aryl; R2 represents C1-C6-alkyl, C1-Csub

Synthesis and conformational analysis of 2′-fluoro-5-methyl-4′- thioarabinouridine (4′S-FMAU)

An improved synthesis of 2′-deoxy-2′-fluoro-5-methyl-4′- thioarabinouridine (4′S-FMAU) is described. Participation of the 3′-O-benzoyl protecting group in the thiosugar precursor influenced the stereochemistry of the N-glycosylation reaction in nonpolar s