117238-30-9

Upstream product

• 117238-29-6 3-O-benzyl-6-deoxy-1,2-O-isopropylidene-5-O-methylsulfonyl-α-D-allofuranose 
• 171762-91-7 Toluene-4-sulfonic acid (R)-1-((3aR,5S,6R,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethyl ester 
• 100-39-0 benzyl bromide 
• 117257-22-4 3-O-benzyl-1,2-O-isopropylidene-6-O-p-toluenesulfonic-α-D-allofuranose 
• 70632-45-0 (R)-1-((3aR,5R,6R,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)ethanol 

Downstream Products

• 117238-31-0 (3R,4S,5R)-5-((S)-1-Azido-ethyl)-4-benzyloxy-3-hydroxy-dihydro-furan-2-one 
• 99212-30-3 deoxyfuconojirimycin 
• 117238-34-3 L-fuconic-δ-lactam 
• 117238-35-4 (2S,3R,4S,5R)-4-Benzyloxy-2-methyl-piperidine-3,5-diol 
• 117238-33-2 (3S,4R,5R,6S)-4-Benzyloxy-3,5-dihydroxy-6-methyl-piperidin-2-one 
• 117238-32-1 5-azido-3-O-benzyl-5-deoxy-L-fucono-1,4-lactone 
• 171762-97-3 1-[(2R,3R,4R,5R)-5-((S)-1-Azido-ethyl)-4-benzyloxy-3-methoxy-tetrahydro-furan-2-yl]-3-(4-methoxy-benzyloxymethyl)-5-methyl-1H-pyrimidine-2,4-dione 
• 171762-98-4 1-[(2R,3R,4R,5R)-5-((S)-1-Amino-ethyl)-4-benzyloxy-3-methoxy-tetrahydro-furan-2-yl]-3-(4-methoxy-benzyloxymethyl)-5-methyl-1H-pyrimidine-2,4-dione 
• 171762-93-9 Acetic acid (3R,4R,5R)-2-acetoxy-5-((S)-1-azido-ethyl)-4-benzyloxy-tetrahydro-furan-3-yl ester 

Relevant academic research and scientific papers

Amide-Modified Oligonucleotides with Preorganized Backbone and Furanose Rings: Highly Increased Thermodynamic Stability of the Duplexes Formed with their RNA and DNA Complements

The amide backbone modification C3′-CH2-CONH-C5′ has been further modified by introducing a methyl at C5′, either in R or in S configuration. Only the S stereoisomer can adopt the required geometry to fit into a duplex with complementary RNA. A

Method of inhibiting virus

A group of five- and six-membered heterocyclic compounds having a nitrogen in the ring and 2 to 3 hydroxyl substituents on the ring are effective inhibitory agents of human immunodeficiency virus.