73591-56-7

Usage

InChI:InChI=1/C10H13N5O5/c11-5-1-3-6(9(19)12-5)13-14-15(3)10-8(18)7(17)4(2-16)20-10/h1,4,7-8,10,14,16-18H,2H2,(H2,11,12,19)

Upstream product

• 51970-31-1 (2R,3R,4S,5R)-2-azido-5-hydroxymethyl-tetrahydro-furan-3,4-diol 
• 1830-54-2 3-oxopentanedioic acid dimethyl ester 
• 6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 73591-44-3 Methyl 5-Methoxycarbonylmethyl-1-(2,4-dinitroanilino)-1,2,3-triazole-4-carboxylate 
• 73591-43-2 Dimethyl 1,3-Acetonedicarboxylate (2,4-Dinitrophenyl)hydrazone 
• 73591-45-4 Methyl 4⁽⁵⁾Methoxycarbonylmethyl-1,2,3-triazole-5⁽⁴⁾carboxylate 
• 73591-47-6 Methyl 4(5)Carbamoylmethyl-1,2,3-triazole-5(4)carboxylate 
• 73591-48-7 Methyl 4(5)Cyanomethyl-1,2,3-triazole-5(4)carboxylate 
• 76143-45-8 methyl 5-(α-chloro-α-cyanomethyl)-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-v-triazole-4-carboxylate 
• 76143-43-6 methyl 5-(α-cyano-α-hydroxymethyl)-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-v-triazole-4-carboxylate 
• 76143-39-0 methyl 5-hydroxymethyl-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-v-triazole-4-carboxylate 
• 76143-42-5 methyl 5-formyl-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-v-triazole-4-carboxylate 
• 135997-83-0 1-((2R,3R,4R,5R)-3,4-Bis-benzoyloxy-5-benzoyloxymethyl-tetrahydro-furan-2-yl)-5-methoxycarbonylmethyl-1H-[1,2,3]triazole-4-carboxylic acid methyl ester 
• 233684-91-8 5-Carbamoylmethyl-1-((2R,3R,4R,5R)-3,4-diacetoxy-5-acetoxymethyl-tetrahydro-furan-2-yl)-1H-[1,2,3]triazole-4-carboxylic acid methyl ester 

Relevant academic research and scientific papers

Synthesis of 8-aza-3-deazaisoguanosine by a novel ring closure of dinitriles by sodium alkoxides

This communication describes a convenient, direct ring closure of a novel 4-cyano-5-cyanomethyl-1-(β-D-ribofuranosyl)-1,2,3-triazole under basic conditions into 4-amino-6-alkoxy-1-(β-D-ribofuranosyl)-1,2,3-triazolo[4,5- c]pyridine, which can be easily tra

An efficient stereospecific method for the synthesis of 8-aza-3-deazaguanine nucleosides from glycosyl azides

8-aza-3-deazaguanine nucleosides 8 were prepared from glycosyl azides 1 via a stereospecific Dimroth reaction with dimethyl 3-oxoglutarate, followed by selective manipulation of the 1,2,3-triazole C-4 and 5 substituents. Of the two methods evaluated for t