133635-08-2

Upstream product

• 133634-97-6 methyl (methyl 4-O-benzyl-3-deoxy-7,8-O-isopropylidene-5-O-methyl-α-D-manno-oct-2-ulopyranosid)onate 
• 114729-36-1 (2R,4R,5R,6S)-4-Benzyloxy-6-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-5-hydroxy-2-methoxy-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 111833-94-4 methyl 4-O-benzyl-3-deoxy-7,8-O-isopropylidene-α-D-manno-oct-2-ulopyrano-sidono-1,5-lactone 
• 133635-00-4 methyl (methyl 3-deoxy-5-O-methyl-α-D-manno-oct-2-ulopyranosid)onate 
• 93-97-0 benzoic acid anhydride 

Downstream Products

• 133635-12-8 methyl (methyl 3-deoxy-5,7,8-tri-O-methyl-α-D-manno-oct-2-ulopyranosid)onate 4-(diphenyl phosphate) 
• 133635-10-6 methyl (methyl 4-O-benzoyl-3-deoxy-5,7,8-tri-O-methyl-α-D-manno-oct-2-ulopyranosid)onate 
• 133635-09-3 methyl (methyl 4-O-benzoyl-3-deoxy-5-O-methyl-α-D-manno-oct-2-ulopyranosid)onate 

Relevant academic research and scientific papers

Phosphorylated Sugars. Part 27. Synthesis and Reactions, in Acid Medium, of 5-O-Substituted Methyl 3-Deoxy-α-D-manno-oct-2-ulopyranosidonic Acid 4-Phosphates

Synthesis of the α-methyl glycosides of 5-O-methyl-, 5-O-benzyl-8-O-methyl-, and 5,7,8-tri-O-methyl-3-deoxy-D-manno-oct-2-ulosonic acid 4-phosphates are described.The corresponding 'reducing' glycose, formed upon hydrolysis at pH 4 and 100 deg C, immediat