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Issue 13, 1996
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Parasite glycoconjugates. Part 5. Blockwise approach to oligo(glycosyl phosphates): chemical synthesis of a terminal tris(glycobiosyl phosphate) fragment of Leishmania donovani antigenic lipophosphoglycan

Andrei V. Nikolaev,  Trevor J. Rutherford,  Michael A. J. Ferguson  and  John S. Brimacombe 

Abstract

The model tetramannosyl triphosphate 7 and the hexaglycosyl triphosphate 8, which is a terminal fragment of the phosphoglycan portion of Leishmania donovani lipophosphoglycan, have been synthesized. Elongation of the chain was performed using the glycosyl hydrogenphosphonate method to couple together two phosphodiester blocks.

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Article type: Paper
DOI: 10.1039/P19960001559
Citation: J. Chem. Soc., Perkin Trans. 1, 1996,0, 1559-1566
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    Parasite glycoconjugates. Part 5. Blockwise approach to oligo(glycosyl phosphates): chemical synthesis of a terminal tris(glycobiosyl phosphate) fragment of Leishmania donovani antigenic lipophosphoglycan

    A. V. Nikolaev, T. J. Rutherford, M. A. J. Ferguson and J. S. Brimacombe, J. Chem. Soc., Perkin Trans. 1, 1996, 0, 1559
    DOI: 10.1039/P19960001559

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