143834-54-2

Upstream product

• 117252-95-6 2-(trimethylsilyl)ethyl β-D-galactopyranoside 
• 824-94-2 p-methoxybenzyl chloride 

Downstream Products

• 299424-55-8 2-(trimethylsilyl)ethyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl-(1->6)-2,4-di-O-benzyl-3-O-p-methoxybenzyl-β-D-galactopyranoside 
• 299424-56-9 2-(trimethylsilyl)ethyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl-(1->6)-2,4-di-O-benzyl-β-D-galactopyranoside 
• 299424-47-8 2-(trimethylsilyl)ethyl 2,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-3-O-p-methoxybenzyl-β-D-galactopyranoside 
• 299424-48-9 2-(trimethylsilyl)ethyl 2,4-di-O-benzyl-3-O-p-methoxybenzyl-β-D-galactopyranoside 
• 509085-99-8 Diazo-acetic acid (2R,3S,4S,5R,6R)-3,5-bis-benzyloxy-2-benzyloxymethyl-6-(2-trimethylsilanyl-ethoxy)-tetrahydro-pyran-4-yl ester 
• 143571-58-8 2-(Trimethylsilyl)ethyl 2,4,6-tri-O-benzyl-β-D-galactopyranoside 
• 678995-74-9 2-(trimethylsilyl)ethyl 2-O-benzoyl-4,6-O-benzylidene-3-O-(4-methoxybenzyl)-β-D-galactopyranoside 
• 678995-83-0 Benzoic acid (2S,4aR,6R,7R,8S,8aS)-2-phenyl-8-trifluoromethanesulfonyloxy-6-(2-trimethylsilanyl-ethoxy)-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester 
• 678995-62-5 2-(trimethylsilyl)ethyl 3-S-acetyl-2-O-benzoyl-4,6-O-benzylidene-β-D-galactopyranoside 
• 678995-60-3 2-(trimethylsilyl)ethyl 2-O-benzoyl-4,6-O-benzylidene-β-D-galactopyranoside 
• 172361-31-8 2-(trimethylsilyl)ethyl 2-O-benzoyl-4,6-O-benzylidene-β-D-galactopyranoside 
• 678995-59-0 2-(trimethylsilyl)ethyl 2-O-benzyl-4,6-O-benzylidene-β-D-galactopyranoside 
• 678995-75-0 2-(trimethylsilyl)ethyl 2-O-benzyl-4,6-O-benzylidene-3-O-(4-methoxybenzyl)-β-D-galactopyranoside 

Relevant academic research and scientific papers

MOENOMYCIN ANALOGS, METHODS OF SYNTHESIS, AND USES THEREOF

The present invention provides novel moenomycin analogs as well as pharmaceutical compositions thereof, methods of synthesis, and methods of use in treating an infection by administering an inventive compound to a subject in need thereof. The moenomycin a

The total synthesis of moenomycin A

Moenomycin A is the only known natural antibiotic that inhibits bacterial cell wall synthesis by binding to the transglycosylases that catalyze formation of the carbohydrate chains of peptidoglycan. We report here the total synthesis of moenomycin A using

Catalytic conversions of diazosugars

Catalytic diazo decomposition chemistry was explored with novel diazoacetate functionalized carbohydrates. In both glucose and galactose derivatives, aromatic cycloadditions with the benzyl protecting groups proved to be most favorable reactions. Replacing the benzyl groups by methoxy groups in the glucose system led to formation of 'carbene dimers'.

Synthetic studies on glycosphingolipids from protostomia phyla: Synthesis of a glycosphingolipid analogue from the parasite Spirometra erinacei

Novel neutral glycosphingolipids isolated from the plerocercoids of a tapeworm, Spirometra erinacei, may be expected to be involved in host-parasite interactions. We have synthesized this glycosphingolipid analogue containing 2-branched fatty alkyl residu