37091-13-7

Upstream product

• 98-88-4 benzoyl chloride 
• 37091-12-6 methyl 3-amino-2,3,6-trideoxy-3-C-methyl-α-L-lyxo-hexopyranoside 
• 109978-72-5 ((2S,3S,6R)-3-Hydroxy-6-methoxy-2,4-dimethyl-tetrahydro-pyran-4-yl)-carbamic acid tert-butyl ester 
• 61199-73-3 methyl 2,3-O-benzylidene-6-deoxy-α-L-mannopyranoside 
• 68673-58-5 (2S,3S)-3-hydroxy-2-methyl-2H-pyran-4(3H)-one 
• 70717-87-2 1,5-anhydro-1,2,6-trideoxy-3-C-methyl-L-ribo-hex-1-enitol 
• 100017-90-1 Methyl-2,3,6-tridesoxy-3-C-methyl-α-L-erythro-hex-2-enopyranosid 
• 1178564-86-7 methyl 4-O-acetyl-2,3,6-trideoxy-3-C-methyl-L-erythro-hex-2-enopyranoside 
• 263327-91-9 methyl 2,3,6-trideoxy-3-C-methyl-α-L-threo-hex-2-enopyranoside 
• 263327-93-1 methyl 4-O-(N,N-dimethyl-1-oxa-3-azo-prop-2-eno)-2,3,6-trideoxy-3-C-methyl-α-L-threo-hexopyranoside 
• 263327-92-0 2-((2S,3S,6R)-6-Methoxy-2,4-dimethyl-3,6-dihydro-2H-pyran-3-yl)-1,1-dimethyl-isourea 
• 263327-90-8 methyl 2,3,6-trideoxy-3-C-methyl-4-O-(4-nitrobenzoyl)-α-L-threo-hex-2-enopyranoside 
• 34819-86-8 3,4-di-O-acetyl-6-deoxy-L-glucal 
• 79026-51-0 methyl 3-acetamido-4-O-acetyl-2,3,6-trideoxy-3-C-methyl-α-L-lyxo-hexopyranoside 

Relevant academic research and scientific papers

Synthesis of methyl α-L-vancosaminide

The synthesis of methyl α-L-vancosaminide from di-O-acetyl-L-rhamnal is described. The allylic alcohol methyl 2,3,6-trideoxy-3-C-methyl-α-L-threo- hex-2-enopyranoside was prepared from the glycal, 1,5-anhydro-1,2,6-trideoxy- 3-C-methyl-L-ribo-hex-1-enitol

Enolates of Carbohydrates, 6. - New Syntheses of Derivatives of 3-Amino-2,3,6-trideoxy-3-C-methyl-L-xylo-hexopyranose, L-Vancosamine, D-Rubranitrose, and Precursors of L-Decilonitrose and D-Kijanose

3-C-Methylated products D-and L-12a,b with erythro- and D- and L-13a,b with threo-configuration are obtained by stereoselective α-C-alkylation of 3-amino-2,3,6-trideoxy-4-uloses D- and L-10a,b.Reduction at low temperatures with L-selectride generates the

Structural investigation of the antibiotic sporaviridin. VI. Structures of individual sugar components

The structural assignment of each of five sugar components from a basic antibiotic, sporaviridin, is described: two are neutral monosaccharides, D-quinovose and D-glucose, and the remaining three are amino sugars, D-visoamine, D-acosamine and L-vancosamin