620172-07-8Relevant articles and documents
Bifunctional antibiotics for targeting rRNA and resistance-causing enzymes
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Page/Page column 9-10, (2010/02/10)
A novel group of aminoglycosides which share some structural features of currently available aminoglycosides with regard to the backbone, while also having significant structural differences. The similarity enables these aminoglycosides to be highly poten
Synthesis of (R)-4,6-O-pyruvated trisaccharide related to the repeating unit of the antigen from Shigella dysenteriae type 9 in the form of its 2-(trimethylsilyl)ethyl glycoside
Roy, Samarpita,Sarkar, Sujit Kumar,Roy, Nirmolendu
, p. 137 - 140 (2007/10/03)
Starting from D-galactose, and D-mannose a trisaccharide namely 2-(trimethylsilyl)ethyl-2,3-di-O-benzoyl-4,6-O-[(R)-1-methoxycarbonylethylidene] -β-D-galactopyranosyl-(1→4)-2, 3, 6-tri-O-benzyl-β-D- mannopyranosyl-(1→4)-2,6-di-O-benzyl-3-O-(4-methoxybenzy
A new class of branched aminoglycosides: Pseudo-pentasaccharide derivatives of neomycin B
Fridman, Micha,Belakhov, Valery,Yaron, Sima,Baasov, Timor
, p. 3575 - 3578 (2007/10/03)
[Equation presented] The clinically important antibiotic neomycin B was modified at position C5″ by adding one extra sugar ring in the β-configuration, and the observed pseudo-pentasaccharides were tested against various bacterial strains, including patho
Programmable one-pot oligosaccharide synthesis
Zhang, Zhiyuan,Ollmann, Ian R.,Ye, Xin-Shan,Wischnat, Ralf,Baasov, Timor,Wong, Chi-Huey
, p. 734 - 753 (2007/10/03)
In an effort to develop a broadly applicable approach to the facile one- pot synthesis of oligosaccharides, the reactivity of a number of p- methylphenyl thioglycoside (STol) donors which are either fully protected or have one hydroxyl group exposed has b