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dc.date.accessioned 2021-12-07T18:50:45Z
dc.date.available 2021-12-07T18:50:45Z
dc.date.issued 2003
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/129282
dc.description.abstract The sulfonamidoglycosylation of benzylated glycals using a catalytic amount of triphenylphosphine hydrobromide proceeded in a highly stereoselective fashion to give the β anomers with good to high yields. This process was demonstrated with D-galactal and D-glucal. Two of the new N-2-(deoxyglycosyl)sulfonamides were tested as inhibitors of tumor cell growth in vitro and showed antiproliferative properties in the micromolar range. en
dc.format.extent 4509-4511 es
dc.language en es
dc.subject Addition reactions es
dc.subject Catalysts es
dc.subject Inhibitors es
dc.subject Sulfones es
dc.subject Pharmaceuticals es
dc.title A Novel Sulfonamidoglycosylation of Glycals en
dc.type Articulo es
sedici.identifier.other https://doi.org/10.1021/ol035838g es
sedici.identifier.issn 1523-7060 es
sedici.identifier.issn 1523-7052 es
sedici.creator.person Colinas, Pedro Alfonso es
sedici.creator.person Bravo, Rodolfo Daniel es
sedici.subject.materias Química es
sedici.description.fulltext true es
mods.originInfo.place Laboratorio de Estudio de Compuestos Orgánicos es
sedici.subtype Articulo es
sedici.rights.license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
sedici.rights.uri http://creativecommons.org/licenses/by-nc-sa/4.0/
sedici.description.peerReview peer-review es
sedici.relation.journalTitle Organic Letters es
sedici.relation.journalVolumeAndIssue vol. 5, no. 23 es


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Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) Excepto donde se diga explícitamente, este item se publica bajo la siguiente licencia Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)