138857-62-2

Upstream product

• 98-88-4 benzoyl chloride 
• 53598-03-1 Methyl-2,3-di-O-benzoyl-4,6-O-benzyliden-β-D-galaktopyranosid 
• 3162-96-7 methyl 4,6-O-benzylidene-β-D-galactopyranoside 
• 999-97-3 1,1,1,3,3,3-hexamethyl-disilazane 
• 117124-69-3 methyl 2,3-di-O-benzoyl-β-D-galactopyranoside 
• 75-77-4 chloro-trimethyl-silane 

Downstream Products

• 138857-76-8 (R)-4-((2S,3S,4R,5R)-3,4-Bis-benzoyloxy-5-methoxy-tetrahydro-furan-2-yl)-2-methyl-[1,3]dioxolane-2-carboxylic acid methyl ester 
• 138857-75-7 methyl 2,3-di-O-benzoyl-4,6-O-<(R)-1-methoxycarbonylethylidene>-1-thio-α-D-galactopyranoside 
• 129192-92-3 methyl 2,3-di-O-benzoyl-4,6-O-<(R)-1-methoxycarbonylethylidene>-β-D-galactopyranoside 
• 138857-78-0 (2S,4aR,6R,7R,8S,8aS)-7,8-Bis-benzoyloxy-6-methoxy-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxine-2-carboxylic acid methyl ester 

Relevant academic research and scientific papers

Syntheses and NMR Studies of Pyruvic Acid 4,6-Acetals of some Methyl Hexopyranosides

The pyruvic acid 4,6-acetals of the methyl glycosides of α- and β-D-glucose, α- and β-D-mannose, and α- and β-D-galactose which correspond to naturally occurring residues in polysaccharides, have been synthesized and their 1H and 13C NMR spectra fully ass

Lewis Acid-Catalysed Anomerisation and Rearrangement of Alkyl D-Glycopyranosides During Acetalisation with Methyl Pyruvate: How to Utilise it for the Preparation of 1-(Carboxyethylidene)glycopyranosyl Donors

The preparation of 4,6-O-(1-methoxycarbonylethylidene)-D-glycopyranosides 5 starting from 2,3-di-O-benzoyl-D-glycopyranosides 1 and their 4,6-bis-O-trimethylsilyl ethers 2 using methyl 2,2-bis(phenylthio)propionate (4) and methyl pyruvate (3), respectivel