168644-99-3Relevant academic research and scientific papers
Synthesis of analogues of calicheamicin and neocarzinostatin chromophore
Cirla, Alessandra,McHale, Angela R.,Mann, John
, p. 4019 - 4029 (2007/10/03)
The work presents a synthetic route to the CD ring of calicheamicin and in the case of neocarzinostatin an approach to a functionalised cyclopentane-1,3-diol containing the naturally occurring naphthoate and a glucosamine motif. In the case of the NCS derivative some biological activity (cytotoxicity) was observed.
New effective synthesis of (N-acetyl- and N-stearoyl-2-amino-2-deoxy-β-D-glucopyranosyl)-(1→4)N-acetyln or-muramoyl-L-2-aminobutanoyl-D-isoglutamine, analogs of GMDP with immunopotentiating activity
Ledvina, Miroslav,Zyka, Daniel,Jezek, Jan,Trnka, Tomas,Saman, David
, p. 577 - 589 (2007/10/03)
Ethyl 3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside (5), prepared by benzylation of ethyl 2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside (4), was transformed by reaction with bromine into 3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-
Synthesis of fully and partially benzylated glycosyl azides via thioalkyl glycosides as precursors for the preparation of N-glycopeptides
Kerekgyarto, Janos,Agoston, Karoly,Batta, Gyula,Kamerling, Johannis P.,Vliegenthart, Johannes F. G.
, p. 7189 - 7192 (2007/10/03)
Fully O-benzylated mono-, di- and trisaccharide glycosyl azides representing the reducing terminal of the core structure of N-glycans were synthesized. Totally and partially benzylated thioalkyl glucosamine glycosides were converted into the corresponding
