20881-87-2

Usage

InChI:InChI=1/C7H15NO4/c1-3-4(8)5(9)6(10)7(11-2)12-3/h3-7,9-10H,8H2,1-2H3/t3-,4-,5+,6+,7+/m1/s1

Upstream product

• 20197-44-8 Methyl 4-acetamido-2,3-di-O-acetyl-4,6-dideoxy-α-D-mannopyranoside 
• 115479-44-2 methyl 6-deoxy-2,3-O-isopropylidene-4-O-trifluoromethanesulfonyl-α-D-talopyranoside 
• 116249-66-2 pradimicin C 
• 15814-59-2 (2S,3S,4S,5S,6R)-2-methoxy-6-methyltetrahydro-2H-pyran-3,4,5-triol 
• 116786-64-2 Methyl 4-Bromo-4,6-dideoxy-α-D-talopyranoside 
• 115479-45-3 methyl 4-azido-4,6-dideoxy-2,3-O-isopropylidene-α-D-mannopyranoside 
• 22932-34-9 methyl 6-deoxy-6-iodo-2,3-O-isopropylidene-α-D-mannopyranoside 
• 20881-79-2 methyl 3,4-anhydro-6-deoxy-α-D-talopyranoside 
• 10515-99-8 methyl 6-deoxy-2,3-O-isopropylidene-4-O-(p-tolylsulfonyl)-α-D-mannopyranoside 
• 135216-54-5 methyl 6-deoxy-4-O-(p-tolylsulfonyl)-α-D-mannopyranoside 
• 141232-01-1 Methyl 4-azido-4-deoxy-2,3-O-isopropylidene-6-O-p-toluenesulfonyl-α-D-mannopyranoside 
• 15856-44-7 Methyl 4-acetamido-4,6-dideoxy-2,3-O-isopropylidene-α-D-mannopyranoside 
• 92735-13-2 methyl 4-azido-4-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside 
• 14133-63-2 methyl 2,3-O-isopropylidene-α-D-rhamnopyranoside 

Downstream Products

• 101072-27-9 Methyl 2,3-di-O-acetyl-4,6-dideoxy-4-<(1S)-(1,4/5,6)-4,5,6-triacetoxy-3-(benzoyloxymethyl)-2-cyclohexen-1-ylamino>-α-D-mannopyranoside 
• 92567-48-1 Methyl 2,3-di-O-acetyl-4,6-dideoxy-4-<(1S)-(1,4/2,3,5)-2,3,4-triacetoxy-5-(acetoxymethyl)-1-cyclohexylamino>-α-D-mannopyranoside 
• 15856-45-8 methyl 4-acetamido-4,6-dideoxy-α-D-mannopyranoside 
• 141316-50-9 Methyl 4,6-dideoxy-4-<(1S)-(1,4/5,6)-4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-ylamino>-α-D-mannopyranoside 
• 116786-66-4 Methyl 4,6-Dideoxy-4-<(S)-2,4-dihydroxybutanamido>-α-D-mannopyranoside 
• 116786-66-4 methyl 4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-α-D-mannopyranoside 

Relevant academic research and scientific papers

Synthesis of the Methyl α-D-Glycosides of Amicetose, Perosamine and Janose

New methods for the synthesis of tri- and di-deoxy sugar, namely methyl α-D-amicetoside, methyl α-D-perosaminoside and methyl α-D-janoside are described.The readily available methyl 6-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside has been used as chiral

Synthesis and enzyme-inhibitory activity of methyl acarviosin analogues having the α-manno configuration

Two methyl acarviosin analogues 3a and 4a, having the α-manno configuration, and their dihydro derivatives 6a and 7a were synthesized by coupling the protected pseudo-sugar epoxides with methyl 4-amino-4-deoxy- and -4,6-dideoxy-α-D-mannopyranoside.Similar

Synthesis and Nuclear Magnetic Resonance Studies of Some N-Acylated Methyl 4-Amino-4,6-dideoxy-α-D-mannopyranosides

The methyl α-glycosides of 4-amino-4,6-dideoxy-D-mannopyranose (perosamine), N-acylated with either formic, acetic, or (S)-2,4-dihydroxybutanoic acid, have been synthesized.The (1)H and (13)C n.m.r. spectra of these substances and the parent, non-N-acylated glycoside, demonstrated how the chemical shifts are influenced by the N-acylation.The N-formyl derivative occured in two conformations, s-cis and s-trans, and the free-energy barrier between these, 86.9 kJ mol-1, was defined by dynamic n.m.r. spectroscopy.

SYNTHESIS OF ANTIGENIC DETERMINANTS OF THE Brucella A ANTIGEN, UTILIZING METHYL 4-AZIDO-4,6-DIDEOXY-α-D-MANNOPYRANOSIDE EFFICIENTLY DERIVED FROM D-MANNOSE

A strategy for the synthesis of Brucella O-antigenic determinants containing 2-linked 4,6-dideoxy-4-formamido-α-D-mannopyranosyl residues is described.The approach adopted also permits the N-acyl moiety to be varied.A high-yield synthesis of methyl 4-azid

Tallysomycin, a new antitumor antibiotic complex related to bleomycin. II. Structure determination of tallysomycins A and B

The structures of tallysomycins A and B, two major components of a new antitumor antibiotic complex, have been determined. They are glycopeptide antibiotics structurally related to bleomycin: four amino acid moieties and a disaccharide fragment which are the constituents of bleomycin molecule are also present in the tallysomycins. Tallysomycins A and B contain two new amino acids and a unique amino sugar, 4-amino-4,6-dideoxy-L-talose, which have not been hitherto found in the phleomycin-bleomycin group of antibiotics. In addition tallysomycin A has an additional amino acid, L-β-lysine, and thus a longer peptide chain than bleomycin or tallysomycin B. Tallysomycins A and B have the same terminal amine moiety, spermidine.