6160-49-2

Upstream product

• 6160-50-5 3,5-di-O-benzyl-2-deoxy-D-ribofuranose 
• 108-24-7 acetic anhydride 
• 132487-16-2 methyl 3,5-di-O-benzyl-2-deoxy-D-ribofuranoside 
• 100-39-0 benzyl bromide 
• 100-44-7 benzyl chloride 
• 51255-17-5 1-O-methyl-2-deoxy-D-ribofuranoside 

Downstream Products

• 51255-13-1 3-(O³,O⁵-dibenzyl-ξ-D-erythro-2-deoxy-pentofuranosyl)-3H-[1,3]oxazine-2,6-dione 
• 115494-00-3 2-((2R,4S,5R)-4-Benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-1-phenyl-ethanone 
• 115493-99-7 2-((2S,4S,5R)-4-Benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-1-phenyl-ethanone 
• 270918-00-8 (2R,3S)-3-Benzyloxy-2-benzyloxymethyl-5-chloro-tetrahydro-furan 
• 78138-02-0 1-(3,5-di-O-benzyl-2-deoxy-α,β-D-erythro-pentofuranosyl)thymine 
• 170983-98-9 1β-cyano-3,5-di-O-benzyl-1,2-dideoxy-D-ribofuranose 
• 226232-74-2 1α-cyano-3,5-di-O-benzyl-1,2-dideoxy-D-ribofuranose 
• 226232-79-7 3,5-Di-O-benzyl-2-desoxy-β-D-ribofuranose-1-imidocarbonsaeuremethylester 
• 226232-77-5 3,5-Di-O-benzyl-2-desoxy-α-D-ribofuranose-1-imidocarbonsaeuremethylester 
• 226232-83-3 5-(3',5'-Di-O-benzyl-2'-desoxy-β-D-ribofuranosyl)-3,6-bis(trifluoromethyl)-1,2,4-triazin 
• 226232-81-1 5-(3',5'-Di-O-benzyl-2'-desoxy-α-D-ribofuranosyl)-3,6-bis(trifluoromethyl)-1,2,4-triazin 
• 137121-87-0 α/β-D-thymidine 
• 78138-03-1 1-(3,5-di-O-benzyl-2-deoxy-α-D-erythro-pentofuranosyl)thymine 
• 78138-00-8 1-<3,5-di-O-benzyl-2-deoxy-α,β-D-erythro-pentofuranosyl>-5,6-dihydro-5-N-methyl-s-triazine-2,4-(3H)-dione 

Relevant academic research and scientific papers

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.

Stereoselective β-C- and β-S-Glycosylation of 2-Deoxyribofuranose Derivatives Controlled by the 3-Hydroxy Protective Group

β-C-2-Deoxyribofuranosides and β-S-2-deoxyribofuranosides are prepared stereoselectively from 1-O-acetyl-5-O-benzyl-3-O--2-deoxy-D-erythro-pentofuranose or the corresponding 3-O-(2-pyridylmethyl)pentofuranose N-oxide by the reacti

STEREOCHEMICAL CONTROL AS A FUNCTION OF PROTECTING-GROUP PARTICIPATION IN 2-DEOXY-D-ERYTHRO-PENTOFURANOSYL NUCLEOSIDES

Possible features controlling the anomeric ratios in the synthesis of the antiviral antibiotic dihydro-5-azathymidine have been examined.Replacement of the 3- and 5-(4-methylbenzoyl) protecting groups in 2-deoxy-D-erythro-pentofuranosyl chloride by benzyl