142952-68-9

Upstream product

• 98-88-4 benzoyl chloride 
• 88410-51-9 D-erythro-3-deoxy-pentose 
• 100-39-0 benzyl bromide 
• 4495-06-1 (3R,5S)-5-((S)-1,2-Dihydroxy-ethyl)-tetrahydro-furan-2,3-diol 
• 143037-49-4 α-D-1,2:5,6-di-O-isopropylidene-3-O-[(methylthio)thiocarbonyl]-glucofuranose 
• 114861-25-5 (3R,5S)-5-(benzyloxymethyl)tetrahydrofuran-2,3-diol 
• 81097-00-9 3-deoxy-1,2:5,6-di-O-isopropylidene-α-D-ribo-hexofuranose 
• 582-52-5 1,2:5,6-diacetone-D-glucose 
• 142941-46-6 methyl 2-O-benzoyl-5-O-benzyl-3-deoxy-D-erythropentofuranoside 
• 132813-61-7 (3R,5S)-5-Benzyloxymethyl-2-methoxy-tetrahydro-furan-3-ol 
• 142941-49-9 (2R,4S)-2-benzoyloxy-5-(benzyloxy)pentane-1,4-diol 
• 124-63-0 methanesulfonyl chloride 

Downstream Products

• 142941-59-1 (3'R,5')-1-<5'-(hydroxymethyl)tetrahydro-3'-thienyl>-5-methylpyrimidine-2,4(1H,3H)-dione 
• 142941-51-3 (2R,4S)-2-<(benzyloxy)methyl>-4-<(methylsulfonyl)oxy>tetrahydrothiophene 
• 142952-69-0 6-amino-9-[(3R,5R)-5-(hydroxymethyl)tetrahydrothiophen-3-yl]purine 
• 142941-60-4 (2R,4R)-4-(2'-amino-6'-chloro-9'H-purin-9'-yl)tetrahydrothiophene-2-methanol 
• 132813-67-3 (2R,4S)-4-benzoyloxy-2-<(benzyloxy)methyl>tetrahydrothiophene 
• 142941-53-5 (3'R,5'R)-4-amino-1-<5'-<(benzyloxy)methyl>tetrahydro-3'-thienyl>pyrimidin-2(1H)-one 
• 142941-52-4 (3'R,5'R)-1-<5'-<(benzyloxy)methyl>tetrahydro-3'-thienyl>pyrimidine-2,4-(1H,3H)-dione 
• 142941-54-6 (3'R,5'R)-1-<5'-<(benzyloxy)methyl>tetrahydro-3'-thienyl>5-methylpyrimidine-2,4-(1H,3H)-dione 
• 142941-55-7 (3'R,5'R)-1-<5'-<(benzyloxy)methyl>tetrahydro-3'-thienyl>-9H-purin-6-amine 
• 142941-56-8 (3'R,5'R)-1-<5'-<(benzyloxy)methyl>tetrahydro-3'-thienyl>-6-chloro-9H-purin-6-amine 
• 132813-66-2 (3S,5R)-5-<(benzyloxy)methyl>tetrahydrothiophen-3-ol 
• 142941-57-9 (3'R,5')-1-<5'-(hydroxymethyl)tetrahydro-3'-thienyl>-pyrimidine-2,4(1H,3H)-dione 
• 142941-57-9 1-[(3R,5R)-5-(hydroxymethyl)tetrahydrothiophen-3-yl]pyrimidine-2,4-dione 
• 132813-66-2 (3R,5R)-5-<(benzyloxy)methyl>tetrahydrothiophen-3-ol 

Relevant academic research and scientific papers

Enantiospecific Synthesis of 3'-Hetero-dideoxy Nucleoside Analogues as Potential Anti-HIV Agents

Two series of analogues of 2',3'-dideoxy carbocyclic nucleosides, in which the 3'-carbon atom is replaced by either an oxygen or a sulfur atom, have been prepared enantiospecifically from diacetone-L-glucose and diacetone-D-glucose respectively.Within eac

TETRAHYDROTHIOPHENE NUCLEOSIDES AS POTENTIAL ANTI-HIV AGENTS

A series of novel tetrahydrothiophene nucleosides have been prepared in homochiral form from D-glucose and assessed as anti-HIV agents in whole cell assay.