dc.contributor.author |
Mandal, P K |
|
dc.date.accessioned |
2015-05-28T06:28:58Z |
|
dc.date.available |
2015-05-28T06:28:58Z |
|
dc.date.issued |
2014 |
|
dc.identifier.citation |
Beilstein Journal of Organic Chemistry, 2014, 10, 2724–2728 |
en |
dc.identifier.uri |
http://hdl.handle.net/123456789/1536 |
|
dc.description.abstract |
The pentasaccharide repeating unit of the O-antigen of E. coli O117:K98:H4 strainhas been synthesizedusing a combination of sequential glycosylations and [3+2] block synthetic strategyfrom the suitably protected monosaccharide intermediates.Thioglycosidesand glycosyltrichloroacetimidatederivativeshave been used as glycosyl donors in the glycosylations. |
en |
dc.format.extent |
202114 bytes |
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dc.format.mimetype |
application/pdf |
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dc.language.iso |
en |
en |
dc.relation.ispartofseries |
CSIR-CDRI Communication No. 8849 |
en |
dc.subject |
Pentasaccharide |
en |
dc.subject |
Escherichia Coli |
en |
dc.subject |
Glycosylation |
en |
dc.subject |
O-antigen |
en |
dc.subject |
Lipopolysaccharide |
en |
dc.title |
Synthesis of the pentasaccharide repeating unit of the O-antigen of E. coli O117:K98:H4 |
en |
dc.type |
Article |
en |