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- W2005045557 abstract "The triflate procedure of Schmidt et al. enabled us to synthesize the glycolipid, 1,2-di-O-stearoyl-3-O-[6-O-(2,3,4-tri-O-benzyl-(3-D-glucopyranosyl)-2,3,4-tri-O-benzyl-ß-D-glucopyranosyl)-2,3,4-tri-O-benzyl-ß-D-glucopyranosyl]-sn-glycerol 1 The prefix sn stands for stereospecific numbering in accordance with the IUPAC recommendation, see: Eur. J. Bio-chem. 2, 127 (1967). . Phosphorylation of this compound with an activated and properly protected phosphatidyl derivative gave a phosphotriester derivative which, after deblocking of all protective groups, afforded a naturally occurring teichoic acid fragment." @default.
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- W2005045557 date "2010-09-02" @default.
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- W2005045557 title "A simple approach to the synthesis of a membrane teichoic acid fragment of Staphylococcus aureus" @default.
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