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Issue 1, 2013
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Concise synthesis of a tetra- and a trisaccharide related to the repeating unit of the O-antigen from Providencia rustigianii O34 in the form of their p-methoxyphenyl glycosides

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Abstract

Concise synthesis of a tetra- and a trisaccharide related to the repeating unit of the O-antigen from Providencia rustigianii O34 is reported. Synthesis of the target oligosaccharides was achieved by rational protecting group manipulations on the commercially available monosaccharides followed by stereoselective glycosylations, using H2SO4-silica for trichloroacetimidate activation and in conjunction with N-iodosuccinimide for thioglycoside activation.

Graphical abstract: Concise synthesis of a tetra- and a trisaccharide related to the repeating unit of the O-antigen from Providencia rustigianii O34 in the form of their p-methoxyphenyl glycosides

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Publication details

The article was received on 05 Oct 2012, accepted on 26 Oct 2012, published on 30 Oct 2012 and first published online on 30 Oct 2012


Article type: Paper
DOI: 10.1039/C2RA22407K
Citation: RSC Adv., 2013,3, 201-207
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    Concise synthesis of a tetra- and a trisaccharide related to the repeating unit of the O-antigen from Providencia rustigianii O34 in the form of their p-methoxyphenyl glycosides

    P. R. Verma and B. Mukhopadhyay, RSC Adv., 2013, 3, 201
    DOI: 10.1039/C2RA22407K

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