134485-39-5

Upstream product

• 24074-26-8 ethyl (diisopropylphosphoryl)acetate 
• 134485-38-4 3,3-dibenzyloxypropanal 
• 134485-30-6 ethyl-3,3-di(benzyl)oxypropanoate 
• 100-51-6 benzyl alcohol 

Downstream Products

• 134485-31-7 5,5-Dibenzyloxy-2E-penten-1-ol 
• 188559-94-6 1-(2-deoxy-β-D-lyxofuranosyl)-5-chlorouracil 
• 188559-08-2 C₂₁H₂₆O₄ 
• 188559-38-8 2-((2R,3R)-5-Benzyloxy-2-methoxymethoxymethyl-tetrahydro-furan-3-yloxy)-5-methyl-3H-pyrimidin-4-one 
• 188559-39-9 2-((2R,3R)-5-Benzyloxy-2-methoxymethoxymethyl-tetrahydro-furan-3-yloxy)-5-fluoro-3H-pyrimidin-4-one 
• 188559-33-3 4-Allyloxy-2-((2R,3R)-5-benzyloxy-2-methoxymethoxymethyl-tetrahydro-furan-3-yloxy)-5-methyl-pyrimidine 
• 188559-34-4 4-Allyloxy-2-((2R,3R)-5-benzyloxy-2-methoxymethoxymethyl-tetrahydro-furan-3-yloxy)-5-fluoro-pyrimidine 
• 188559-06-0 C₃₈H₃₆O₃ 
• 188559-43-5 5'-O-trityl-O²,3'-cycloanhydro-N³-thymidine 
• 188559-40-2 5-Chloro-1-((2R,4R,5R)-4-hydroxy-5-trityloxymethyl-tetrahydro-furan-2-yl)-1H-pyrimidine-2,4-dione 
• 188559-36-6 2-((2R,3R)-5-Benzyloxy-2-trityloxymethyl-tetrahydro-furan-3-yloxy)-3H-pyrimidin-4-one 
• 188559-35-5 2-((2R,3R)-5-Benzyloxy-2-trityloxymethyl-tetrahydro-furan-3-yloxy)-5-methyl-3H-pyrimidin-4-one 
• 188559-37-7 2-((2R,3R)-5-Benzyloxy-2-trityloxymethyl-tetrahydro-furan-3-yloxy)-5-chloro-3H-pyrimidin-4-one 
• 188559-31-1 4-Allyloxy-2-((2R,3R)-5-benzyloxy-2-trityloxymethyl-tetrahydro-furan-3-yloxy)-pyrimidine 

Relevant academic research and scientific papers

Stereocontrolled synthesis of β-2'-deoxypyrimidine nucleosides via intramolecular glycosylations

A pyrimidine moiety was tethered at the 3'-β-position of D-threo-furanosides. By carefully controlling the reaction conditions, pyrimidine bases can be delivered to the anomeric center to give of β-pyrimidine nucleosides in good yield and with complete stereocontrol.

An efficient synthesis of 3′-fluoro-3′-deoxythymidene (FLT)

A synthetic route which permits the regioselective introduction of fluoride into an FLT precursor under mild conditions and the subsequent conversion of that intermediate into FLT is reported.