完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Pradhan, Tapan Kumar | en_US |
dc.contributor.author | Mong, Kwok Kong Tony | en_US |
dc.date.accessioned | 2015-07-21T08:28:50Z | - |
dc.date.available | 2015-07-21T08:28:50Z | - |
dc.date.issued | 2015-04-01 | en_US |
dc.identifier.issn | 0021-2148 | en_US |
dc.identifier.uri | http://dx.doi.org/10.1002/ijch.201400145 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/124697 | - |
dc.description.abstract | 3-Deoxy-D-manno-Oct-2-ulosonic acid (Kdo)-containing oligosaccharides are a conserved carbohydrate component in lipopolysaccharides ( LPSs) of the outer membrane of Gram-negative bacteria, and they are also present in capsular polysaccharides ( CPSs) of bacteria and plant cells. The association of the bacterial LPS with the pathophysiology of bacterial infection have long been recognized. Structure-pathophysiology studies of bacterial infection need to use pure and homogeneous LPS fragments. Such a requirement can be fulfilled by the synthesis of Kdo glycosides and related Kdo-oligosaccharide conjugates. This article provides an overview of the glycosylation chemistries of the synthesis of Kdo alpha-/beta-glycosides, oligosaccharides with Kdo units such as LPS core oligosaccharides, and lipid A derivatives. | en_US |
dc.language.iso | en_US | en_US |
dc.title | Glycosylation Chemistry of 3-Deoxy-D-manno-Oct-2-ulosonic Acid (Kdo) Donors | en_US |
dc.type | Review | en_US |
dc.identifier.doi | 10.1002/ijch.201400145 | en_US |
dc.identifier.journal | ISRAEL JOURNAL OF CHEMISTRY | en_US |
dc.citation.volume | 55 | en_US |
dc.citation.issue | 3-4 | en_US |
dc.citation.spage | 285 | en_US |
dc.citation.epage | 296 | en_US |
dc.contributor.department | 交大名義發表 | zh_TW |
dc.contributor.department | National Chiao Tung University | en_US |
dc.identifier.wosnumber | WOS:000352801400005 | en_US |
dc.citation.woscount | 0 | en_US |
顯示於類別: | 期刊論文 |