154230-40-7

Upstream product

• 154230-39-4 (2R,3S,5R)-benzoic acid 5-(3-benzyloxymethyl-5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-2-hydroxymethyl-tetrahydro-furan-3-yl ester 
• 75-65-0 tert-butyl alcohol 
• 154230-38-3 (2R,3S,5R)-benzoic acid 5-(3-benzyloxymethyl-5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-2-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan-3-yl ester 
• 154230-32-7 5'-O-tert-butyldiphenylsilyl-N³-benzyloxymethyl-2'-deoxythymidine 
• 101527-40-6 5'-O-tert-butyldiphenylsilylthymidine 
• 3587-60-8 Benzyloxymethyl chloride 

Downstream Products

• 154230-42-9 (2S,3S,5R)-benzoic acid 2-acetoxy-5-(3-benzyloxymethyl-5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester 
• 154230-43-0 (2R,3S,5R)-benzoic acid 2-acetoxy-5-(3-benzyloxymethyl-5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester 
• 154230-41-8 (2S,3S,5R)-3-benzoyloxy-5-(3-benzyloxymethyl-5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-carboxylic acid 

Relevant academic research and scientific papers

Nucleic Acid Mimics. Synthesis of Ethylene Glycol- and Propoxy-Linked Thymidyl-Tetrahydrofuranylthymine Dimers via a Vorbrueggen-Type Glycosylation Reaction

Two thymidyl-tetrahydrofuranylthymine dimers, 15 and 16, were synthesized stereospecifically in good yield via a Vorbrueggen-type reaction between glycol ether 4 or propoxy alcohol 7 and acetate 12.