69401-28-1

Upstream product

• 69346-96-9 D-erythro-2,3-hexodiulosono-1,4-lactone 2-(phenylhydrazone) 3-oxime 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 
• 28912-21-2 D-erythro-2,3-hexodiulosono-1,4-lactone 2-(phenylhydrazone) 
• 100-63-0 phenylhydrazine 
• 5959-82-0 D-erythro-2,3-hexodiulosono-1,4-lactone 

Downstream Products

• 69320-73-6 (S)-2-(4-bromo-phenyl)-6-((R)-1,2-diacetoxy-ethyl)-2,6-dihydro-4H-furo[3,4-d][1,2,3]triazol-4-one 
• 65785-06-0 2-phenyl-4-(1,2,3-tri-O-acetyl-D-erythro-glycerol-1-yl)-1,2,3-triazole-5-carboxamide 
• 89157-65-3 2-phenyl-4-formyl-1,2,3-triazole-5-carboxylic acid 5-hydrazide 
• 89157-58-4 2-phenyl-4-(D-erythro-glycerol-1-yl)-1,2,3-triazole-5-carboxylic axid 5-hydrazide 
• 65785-05-9 2-phenyl-4-(D-erythro-glycerol-1-yl)-1,2,3-triazole-5-carboxamide 

Relevant academic research and scientific papers

STUDIES ON DEHYDRO-D-arabino-ASCORBIC ACID 2-ARYLHYDRAZONE 3-OXIMES: CONVERSION INTO SUBSTITUTED TRIAZOLES AND ISOXAZOLINES

D-erythro-2,3-Hexodiulosono-1,4-lactone 2-arylhydrazones (2) were prepared by condensation of dehydro-D-arabino-ascorbic acid with the desired arylhydrazine.Reaction of 2 with hydroxylamine gave the 2-arylhydrazone 3-oximes (3).On boiling with acetic anhy