Linked Life Data

15823005

Source:http://linkedlifedata.com/resource/pubmed/id/15823005

Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:15823005rdf:typepubmed:Citationlld:pubmed
pubmed-article:15823005lifeskim:mentionsumls-concept:C0010580lld:lifeskim
pubmed-article:15823005lifeskim:mentionsumls-concept:C0020233lld:lifeskim
pubmed-article:15823005lifeskim:mentionsumls-concept:C0024746lld:lifeskim
pubmed-article:15823005lifeskim:mentionsumls-concept:C0243077lld:lifeskim
pubmed-article:15823005lifeskim:mentionsumls-concept:C0205250lld:lifeskim
pubmed-article:15823005lifeskim:mentionsumls-concept:C0444454lld:lifeskim
pubmed-article:15823005lifeskim:mentionsumls-concept:C0439831lld:lifeskim
pubmed-article:15823005pubmed:issue8lld:pubmed
pubmed-article:15823005pubmed:dateCreated2005-4-12lld:pubmed
pubmed-article:15823005pubmed:abstractTextA simple diastereoselective access to amino- and hydrazinocyclopentitols is described. The key step involves a cationic rearrangement of a meso bicyclic hydrazine, followed by two successive stereoselective hydroxylations. Both racemic compounds are micromolar alpha-mannosidase (Jack bean) inhibitors.lld:pubmed
pubmed-article:15823005pubmed:languageenglld:pubmed
pubmed-article:15823005pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15823005pubmed:citationSubsetIMlld:pubmed
pubmed-article:15823005pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15823005pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15823005pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15823005pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15823005pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15823005pubmed:statusMEDLINElld:pubmed
pubmed-article:15823005pubmed:monthAprlld:pubmed
pubmed-article:15823005pubmed:issn0022-3263lld:pubmed
pubmed-article:15823005pubmed:authorpubmed-author:BoninMMlld:pubmed
pubmed-article:15823005pubmed:authorpubmed-author:RobicDDlld:pubmed
pubmed-article:15823005pubmed:authorpubmed-author:MicouinLLlld:pubmed
pubmed-article:15823005pubmed:authorpubmed-author:BournaudCClld:pubmed
pubmed-article:15823005pubmed:issnTypePrintlld:pubmed
pubmed-article:15823005pubmed:day15lld:pubmed
pubmed-article:15823005pubmed:volume70lld:pubmed
pubmed-article:15823005pubmed:ownerNLMlld:pubmed
pubmed-article:15823005pubmed:authorsCompleteYlld:pubmed
pubmed-article:15823005pubmed:pagination3316-7lld:pubmed
pubmed-article:15823005pubmed:dateRevised2006-11-15lld:pubmed
pubmed-article:15823005pubmed:meshHeadingpubmed-meshheading:15823005...lld:pubmed
pubmed-article:15823005pubmed:meshHeadingpubmed-meshheading:15823005...lld:pubmed
pubmed-article:15823005pubmed:meshHeadingpubmed-meshheading:15823005...lld:pubmed
pubmed-article:15823005pubmed:meshHeadingpubmed-meshheading:15823005...lld:pubmed
pubmed-article:15823005pubmed:meshHeadingpubmed-meshheading:15823005...lld:pubmed
pubmed-article:15823005pubmed:meshHeadingpubmed-meshheading:15823005...lld:pubmed
pubmed-article:15823005pubmed:meshHeadingpubmed-meshheading:15823005...lld:pubmed
pubmed-article:15823005pubmed:year2005lld:pubmed
pubmed-article:15823005pubmed:articleTitleHighly functionalized cyclopentanes from meso bicyclic hydrazines. A rapid access to mannosidase inhibitors.lld:pubmed
pubmed-article:15823005pubmed:affiliationLaboratoire de Chimie Thérapeutique, UMR 8638 associée au CNRS et à l'Université René Descartes, Faculté des Sciences Pharmaceutiques et Biologiques, 4 av de l'Observatoire, 75270 Paris Cedex 06, France.lld:pubmed
pubmed-article:15823005pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15823005pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed