35812-81-8

Upstream product

• 112146-85-7 benzyl 2-deoxy-2-<(4,4-dimethyl-2,6-dioxocyclohexylidenemethyl)amino>-α-D-glucopyranoside 
• 13343-62-9 benzyl 2-acetamido-2-deoxy-α-D-glucopyranoside 
• 221687-36-1 benzyl 2-deoxy-2-[1-(1,3-dimethyl-2,4,6(1H,3H,5H)-trioxopyrimidin-5-ylidene)phenylmethylamino]-α-D-glucopyranoside 
• 109-73-9 N-butylamine 
• 95451-81-3 Benzyl-2-azido-2-desoxy-α-D-mannoopyranosid 
• 95451-93-7 3,4,6-Tri-O-acetyl-2-azido-2-deoxy-α-D-mannopyranosyl bromide 
• 68733-20-0 1,3,4,6-tetra-O-acetyl-2-azido-2-deoxy-α-D-mannopyranoside 
• 95451-80-2 Benzyl-3,4,6-tri-O-acetyl-2-azido-2-desoxy-α-D-mannopyranosid 
• 100-51-6 benzyl alcohol 
• 2873-29-2 D-glucal triacetate 
• 22323-61-1 Methyl 3,4,6-tri-O-methyl-β-D-galactopyranoside 
• 110911-55-2 Methyl 2-O-allyl-3,4,6-tri-O-methyl-β-D-galactopyranoside 
• 110911-48-3 methyl-2-O-(N-imidazolylsulfonyl)-3,4,6-tri-O-methyl-β-D-galactopyranoside 

Downstream Products

• 117701-85-6 ((2S,3R,4R,5S,6R)-4,5-Diacetoxy-6-acetoxymethyl-2-benzyloxy-tetrahydro-pyran-3-yl)-trimethyl-ammonium; bromide 
• 791064-18-1 ((2S,3R,4R,5S,6R)-2-Benzyloxy-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl)-carbamic acid vinyl ester 
• 1008165-70-5 benzyl 2-(N-acetyl-L-cysteinyl)amino-2-deoxy-α-D-glucopyranoside 
• 1372616-70-0 benzyl 2-deoxy-4,6-O-benzylidene-3-O-(2,2,2-trichloro-ethoxycarbonyl)-2-(2,2,2-trichloro-ethoxycarbonylamino)-α-D-glucopyranoside 
• 1372616-71-1 1,6-di-O-benzyl-2-deoxy-3-O-(2,2,2-trichloro-ethoxycarbonyl)-2-(2,2,2-trichloro-ethoxy-carbonylamino)-α-D-glucopyranoside 
• 1372616-72-2 1,6-di-O-benzyl-4-O-[3,4,6-tri-O-acetyl-2-deoxy-2-(2,2,2-trichloro-ethoxycarbonylamino)-α-D-glucopyranosyl]-3-O-(2,2,2-trichloro-ethoxycarbonyl)-2-deoxy-2-(2,2,2-trichloro-ethoxy-carbonylamino)-α-D-glucopyranoside 
• 1372616-73-3 1,6-Di-O-benzyl-4-O-[3,4,6-tri-O-acetyl-2-acetamido-α-D-glucopyranosyl]-2-acetamido-α-D-glucopyranoside 
• 176019-96-8 benzyl 4,6-O-benzylidene-2-deoxy-2-(2,2,2-trichloro-ethoxycarbonylamino)-α-D-glucopyranoside 
• 10380-86-6 phenylmethyl 2-acetylamino-2-deoxy-α-D-mannopyranoside 
• 42890-09-5 Benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-α-D-mannopyranosid 
• 95451-85-7 (Benzyl-2-acetamido-3-O-benzyl-2-desoxy-α-D-mannopyranosid)uronsaeure 
• 95451-84-6 benzyl-2-acetamido-3-O-benzyl-2-desoxy-α-D-mannopyranosid 
• 3554-91-4 benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-mannopyranoside 
• 95530-21-5 (Benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-α-D-mannopyranosid)uronsaeure 

Relevant academic research and scientific papers

Cross-functionalities of Bacillus deacetylases involved in bacillithiol biosynthesis and bacillithiol-S-conjugate detoxification pathways

BshB, a key enzyme in bacillithiol biosynthesis, hydrolyses the acetyl group from N-acetylglucosamine malate to generate glucosamine malate. In Bacillus anthracis, BA1557 has been identified as the N-acetylglucosamine malate deacetylase (BshB); however, a

Anti-cancer properties and catalytic oxidation of sulfides based on vanadium(V) complexes of unprotected sugar-based Schiff-base ligands

In this article, benzyl 2-deoxy-2-salicylideneamino-α-D-glucopyranoside (H2SalHGlc), a sugar-based Schiff-base ligand, as well as four of its derivatives including H2Sal5-BrGlc, H2Sal3,5-tBu/sup

Cleavage of unactivated amide bonds by ammonium salt-accelerated hydrazinolysis

Hydrazinolysis of unactivated amide bonds is significantly accelerated by the addition of ammonium salts. The reactions proceed at 50-70 °C to give amines with broad substrate scope that outperforms existing amide bond cleavage reactions. Application to peptide and amino sugar derivatives is also demonstrated. This journal is

Synthesis of a 3-hydroxyl-free N-acetyl glucosamine disaccharide

A simple and alternative route to a versatile N-acetyl glucosamine disaccharide building block was developed, possessing a free 3-hydroxyl group. In this strategy, the 2,2,2-trichloro-ethoxy carbonyl (Troc) group was used as an amino-and 3-hydroxyl-protec

Nickel(II) complexes with Schiff-base ligands derived from epimeric pyranose backbones as 2,3-chelators: modeling the coordination chemistry of chitosan

Two mononuclear nickel(II) complexes with Schiff-base ligands derived from the epimeric sugars glucosamine and mannosamine have been synthesized. The X-ray crystal structure reveals a distorted octahedral geometry at the nickel(II) ions with an N4/s

Mycothiol disulfide reductase: Solid phase synthesis and evaluation of alternative substrate analogues

A solid phase synthesis of des-myo-inositol mycothiol disulfide and its alpha-configured methyl- and benzyl-glycoside derivatives has been developed. Kinetic characterisation of these compounds has demonstrated their viability as alternative substrates for use in mycothiol disulfide reductase enzyme assays. This journal is The Royal Society of Chemistry.

Protecting and linking groups for organic synthesis on solid supports

This invention relates to methods for synthesis of organic compounds, and in particular to compounds useful as protecting and linking groups for use in the synthesis of peptides, oligosaccharides, glycopeptides and glycolipids. The invention provides prot

UEBER EINE UNGEWOEHNLICHE REAKTION DER 2-DESOXY-2-TRIMETHYLAMMONIO-D-GLUCOSE

The alkaline hydrolysis of 2-deoxy-1,3,4,6-tetra-O-acetyl-2-trimethylammonio-α-D-glucopyranose chloride leads to an unexpected product.Contrary to the hydrolysis under acidic conditions yielding 2-deoxy-2-trimethylammonio-D-glucose we obtained the corresponding 3,6-anhydro derivative by reaction with sodium hydroxide or ammonia in methanol.

SYNTHESIS OF ALKYL GLYCO-PYRANOSIDES AND -FURANOSIDES OF 2-AMINO-2-DEOXY-D-GLUCOSE. CRYSTAL STRUCTURE OF 2-DEOXY-2--α-D-GLUCOPYRANOSE

The reaction of 2-amino-2-deoxy-D-glucose hydrochloride with 5,5-dimethyl-2-phenylaminomethylene-1,3-cyclohexanedione in MeOH in the presence of Et3N afforded 2-deoxy-2--D-glucose (6) in yields >75percen

REACTIVITE DES N-IMIDAZOLYLSULFONATES EN C-2 D'α-D-MANNO- ET GALACTO-PYRANOSIDES

The imidazolylsulfonyl derivatives of methyl 3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside, methyl 3,4,6-tri-O-benzyl-α-D-mannopyranoside, a lactose derivative 10 protected everywhere except at OH-2', benzyl 6-O-allyl-3,4-O-isopropylidene-α-D-galactopy