207607-14-5

Upstream product

• 180300-89-4 5-O-tert-butyldimethylsilyl-1,2-O-isopropylidene-3-C-ethenyl-α-D-ribofuranose 
• 221227-58-3 (3aR,5R,6R,6aR)-5-(hydroxymethyl)-2,2-dimethyl-6-vinyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol 
• 207606-87-9 1,2-di-O-isopropylidene-3,5-di-O-benzyl-3-C-vinyl-α-D-ribofuranose 
• 103931-45-9 5-O-(tert-butyldimethylsilyl)-1,2-O-isopropylidene-α-D-erythro-pentofuranos-3-ulose 
• 65-71-4 thymin 
• 207607-10-1 1,2-di-O-acetyl-3,5-di-O-benzyl-3-C-vinyl-α,β-D-ribofuranose 

Downstream Products

• 207607-21-4 1-(3,5-di-O-benzyl-3-C-vinyl-β-D-arabinofuranosyl)thymine 
• 207607-18-9 1-(3,5-di-O-benzyl-2-O-methanesulfonyl-3-C-vinyl-β-D-ribofuranosyl)thymine 
• 207606-97-1 1-((2R,3S,4S,5R)-4-Benzyloxy-5-benzyloxymethyl-3-hydroxy-4-hydroxymethyl-tetrahydro-furan-2-yl)-5-methyl-1H-pyrimidine-2,4-dione 
• 207607-26-9 (1R,2R,4R,5S)-1-benzyloxy-2-(benzyloxy)methyl-4-(thymin-1-yl)-3,6-dioxabicyclo[3.2.0]heptane 
• 207606-92-6 N1-(3,5-di-O-benzyl-3-C-vinyl-β-D-ribofuranosyl)thymine 

Relevant academic research and scientific papers

An α-D-configured bicyclic nucleoside restricted in an E-type conformation: Synthesis and parallel RNA recognition

An α-D-arabino configured bicyclic nucleoside strongly restricted in an E-type conformation by a 2′-3′-fused oxetane ring is synthesized. Several synthetic strategies toward the target compound are described, and the successful preparation from a D-xylose

A novel class of oligonucleotide analogues containing 2′-O,3′-C-linked [3.2.0]bicycloarabinonucleoside monomers: Synthesis, thermal affinity studies, and molecular modeling

Oligonucleotide analogues containing a novel 2′-O,3′-C-linked [3.2.0]bicyclonucleoside have been efficiently synthesized. Enhanced thermal stabilities of duplexes toward both RNA and DNA are reported for a 14-mer oligothymidylate containing 13 modificatio