130351-69-8

Upstream product

• 190723-42-3 Methanesulfonic acid (2R,3R,4R,5R)-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-4-methanesulfonyloxy-tetrahydro-furan-3-yl ester 
• 130351-68-7 1-(5-O-tert-butyldiphenylsilyl-β-D-ribofuranosyl)uracil 

Downstream Products

• 190723-65-0 (1R,2S,4R,5S,6R)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-4-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3-oxa-bicyclo[3.1.0]hexane-6-carboxylic acid benzyl ester 
• 190723-64-9 (1R,2S,4R,5S,6S)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-4-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3-oxa-bicyclo[3.1.0]hexane-6-carboxylic acid benzyl ester 
• 190723-67-2 (1R,2S,4R,5S,6R)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-4-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3-oxa-bicyclo[3.1.0]hexane-6-carboxylic acid 
• 190723-66-1 (1R,2S,4R,5S,6S)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-4-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3-oxa-bicyclo[3.1.0]hexane-6-carboxylic acid 
• 190723-62-7 (1S,2S,4R,5R)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-4-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-6-phenylsulfanyl-3-oxa-bicyclo[3.1.0]hexane-6-carboxylic acid benzyl ester 
• 190723-59-2 (1R,2S,4R,5S,6S)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-6-cyano-4-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3-oxa-bicyclo[3.1.0]hexane-6-carboxylic acid benzyl ester 
• 190723-60-5 (1R,2S,4R,5S,6S)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-6-cyano-4-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3-oxa-bicyclo[3.1.0]hexane-6-carboxylic acid 

Relevant academic research and scientific papers

2′,3′-Cyclopropanated Nucleoside Dimers

Syntheses of three novel conformationally rigid dimers containing cyclopropyl -amide and -sulfonamide functionalities are described. Their incorporation into an oligonucleotide sequence resulted in considerable lowering of the Tm's in binding to their complementary RNA sequences.

Synthesis of antiviral activity of 3'-deoxy-3'-C-hydroxymethyl nucleosides

A series of 3'-branched-chain sugar nucleosides, in particular 3'-deoxy-3'-C-hydroxymethyl nucleosides, have been synthesized and evaluated as antiviral agents. Reaction of 1-(2,3-epoxy-5-O-trityl-β-D-lyxo-pentafuranosyl) derivatives 12 and 13, of uracil