110889-33-3

Upstream product

• 110889-30-0 Acetic acid (4aR,6S,6aR,11S,11aS,11bR)-11a-hydroxy-6-methoxy-8,8-dimethyl-2-phenyl-octahydro-1,3,5,7,9-pentaoxa-cyclohepta[a]naphthalen-11-yl ester 
• 110889-28-6 methyl 4,6-O-benzylidene-3-C-<(S)-1,2-dihydroxyethyl>-2,2¹-O-isopropylidene-α-D-glucopyranoside 
• 110889-28-6 methyl 4,6-O-benzylidene-3-C-<(R)-1,2-dihydroxyethyl>-2,2¹-O-isopropylidene-α-D-glucopyranoside 
• 110889-24-2 (4aR,6S,7R,8aS)-8-[2-Hydroxy-eth-(E)-ylidene]-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol 
• 110889-27-5 methyl 4,6-O-benzylidene-3-C-<(Z)-2-hydroxyethylidene>-2,2¹-O-isopropylidene-α-D-ribo-hexopyranoside 
• 110889-31-1 methyl 1¹-O-acetyl-3-C-<(S)-1,2-dihydroxyethyl>-2,2¹-O-isopropylidene-α-D-glucopyranoside 
• 110889-32-2 methyl 1¹-O-acetyl-3-C-<(S)-1,2-dihydroxyethyl>-2,2¹-O-isopropylidene-6-O-pivaloyl-α-D-glucopyranoside 
• 98-59-9 p-toluenesulfonyl chloride 

Relevant academic research and scientific papers

SYTHESIS OF METHYL 4-DEOXY-3-C--α-D-xylo-HEXOPYRANOSIDE AND METHYL 2,21-ANHYDRO-3-C--α-D-GLUCOPYRANOSIDE DERIVATIVES

The title branched-chain sugars possessing a new type of two-carbon branch were synthesised from D-glucose.These compounds are important intermediates for a total synthesis of the nucleoside antibiotics, amipurimycin and miharamycin.