| 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 | |
| dc.format.mimetype | application/pdf | |
| 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 |