226232-74-2

Upstream product

• 6160-49-2 1-O-acetyl-3,5-di-O-benzyl-2-deoxy-D-erythro-pentofuranose 
• 7677-24-9 trimethylsilyl cyanide 
• 452-51-7 D-2-deoxyribose 
• 100-39-0 benzyl bromide 
• 132487-16-2 methyl 3,5-di-O-benzyl-2-deoxy-D-ribofuranoside 
• 51255-17-5 1-O-methyl-2-deoxy-D-ribofuranoside 
• 100-44-7 benzyl chloride 
• 6160-50-5 3,5-di-O-benzyl-2-deoxy-D-ribofuranose 

Downstream Products

• 226232-77-5 3,5-Di-O-benzyl-2-desoxy-α-D-ribofuranose-1-imidocarbonsaeuremethylester 
• 263006-24-2 (2S,4S,5R)-4-Benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-carboxylic acid 
• 263006-32-2 4-((4S,5R)-4-Benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-2-methylsulfanyl-6-octyl-pyrimidine 
• 263006-31-1 4-((4S,5R)-4-Benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-2-methyl-6-octyl-pyrimidine 
• 263006-27-5 1-((2S,4S,5R)-4-Benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-undec-2-yn-1-one 
• 263006-34-4 4-((4S,5R)-4-Benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-2-methylsulfanyl-6-phenyl-pyrimidine 
• 263006-33-3 4-((4S,5R)-4-Benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-2-methyl-6-phenyl-pyrimidine 
• 263006-26-4 1-((2S,4S,5R)-4-Benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-3-trimethylsilanyl-propynone 
• 263006-28-6 1-((2S,4S,5R)-4-Benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-3-phenyl-propynone 
• 263006-30-0 4-((4S,5R)-4-Benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-2-methylsulfanyl-pyrimidine 
• 263006-25-3 (2S,4S,5R)-4-Benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-carboxylic acid methoxy-methyl-amide 
• 263006-38-8 (2R,3S)-2-Hydroxymethyl-5-(2-methyl-6-phenyl-pyrimidin-4-yl)-tetrahydro-furan-3-ol 
• 226232-81-1 5-(3',5'-Di-O-benzyl-2'-desoxy-α-D-ribofuranosyl)-3,6-bis(trifluoromethyl)-1,2,4-triazin 

Relevant academic research and scientific papers

Base pair recognition ability of 2-(methylamino)pyrimidin-4-yl nucleobase in parallel triplex dna

A phosphoramidite bearing a 2-(methylamino)pyrimidin-4-yl nucleobase was synthesized and the modified oligonucleotide (triplex-forming oligonucleotide, TFO) was successfully obtained using the phosphoramidite on an automated DNA synthesizer. UV-melting ex

Synthesis of novel C-nucleosides with potential applications in combinatorial and parallel synthesis

Novel di-substituted pyrimidinyl C-nucleosides have been synthesised using a flexible synthetic methodology. This methodology conveniently allows the synthesis of alpha and beta nucleosides, both of which are of biological interest. Reactive acetylenic ke

Synthesis of novel Pyridine-, Pyrindine- and Isoquinoline-substituted α- and β-C-nucleosides of 2-deoxy-D-ribose

The novel imido esters of 2-deoxy-α- and -β-D-ribose 8 and 9 have been synthesized and successfully transformed to the protected 1,2,4-triazine-C-nucleosides 11 and 12 using an inverse type Diels-Alder reaction with the 1,2,4,5-tetrazine 10. The electron deficient diazadiene system of both C-nucleosides 11 and 12 proved to be highly reactive in a consecutive [4 + 2] cycloaddition with inverse electron demand towards several electron rich dienophiles yielding after successful deprotection the novel pyridine-, pyrindine- and isoquinoline-C-nucleosides 15, 18 and 21 of 2-deoxy-α-D-ribose and 23, 25 and 27 of 2-deoxy-β-D-ribose.