34311-67-6

Upstream product

• 26293-59-4 3-deoxy-3-methylene-1,2-O-(1-methyethylidene)-5-O-(phenylmethyl)-α-D-xylofuranose 
• 6893-65-8 1,2-di-O-isopropylidene-5-O-tosyl-D-xylofuranose 
• 20031-21-4 1,2-O-isopropylidene-α-D-xylose 
• 34311-63-2 5-O-benzyl-3-oxo-1,2-O-isopropylidene-α-D-xylofuranose 
• 23202-83-7 5-benzyl-1,2-O-isopropylidene-α-D-xylofuranose 
• 100-44-7 benzyl chloride 
• 146035-67-8 3-deoxy-3-(hydroxymethyl)-5-O-<(tert-butyldimethyl)silyl>-1,2-O-isopropylidene-α-D-ribofuranose 

Downstream Products

• 1026404-30-7 (3R,4S,5S)-4,5-Bis-benzyloxymethyl-tetrahydro-furan-2,3-diol 
• 132523-62-7 3-deoxy-3-<(phenylmethoxy)methyl>-5-O-(phenylmethyl)-α-D-ribofuranose diacetate 
• 69827-91-4 3-deoxy-1,2-O-(1-methylethylidene)-3-<(phenylmethoxy)methyl>-5-O-(phenylmethyl)-α-D-ribofuranose 
• 604801-36-7 3-[(p-anisyloxy)methyl]-5-O-benzyl-3-deoxy-1,2-O-(isopropylidene)-α-D-ribofuranose 

Relevant academic research and scientific papers

Synthesis and antiviral activity of novel isonucleoside analogs

A series of branched-chain sugar isonucleosides was synthesized and evaluated for antiviral activity against herpesviruses. The preparation of homochiral [3S-(3α,4β,5α)]-2-amino-1,9-dihydro-9-[tetrahydro-4,5- bis(hydroxymethyl)-3-furanyl]-6H-purin-6-one (

3′-C-branched-chain-substituted nucleosides and nucleotides as potent inhibitors of Mycobacterium tuberculosis thymidine monophosphate kinase

Thymidine monophosphate kinase (TMPK) of Mycobacterium tuberculosis (TMPKmt) represents an attractive target for blocking the bacterial DNA synthesis. In an attempt to find high-affinity inhibitors of TMPKmt, a cavity in the enzyme at the 3′-position was

Purinyl tetrahydrofurans

Antiviral activity is exhibited by compounds having the formula STR1 and pharmaceutically acceptable salts thereof wherein R1 is a purine or pyrimidine base or an analog thereof and R2 and R3 are independently hydrogen, --