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https://hdl.handle.net/10495/43565Registro completo de metadatos
| Campo DC | Valor | Lengua/Idioma |
|---|---|---|
| dc.contributor.author | Zapata Londoño, María Bibiana | - |
| dc.contributor.author | Betancur Galvis, Liliana Amparo | - |
| dc.contributor.author | Ramírez, Dámaris | - |
| dc.contributor.author | González Cardenete, Miguel Ángel | - |
| dc.date.accessioned | 2024-11-18T18:02:30Z | - |
| dc.date.available | 2024-11-18T18:02:30Z | - |
| dc.date.issued | 2009 | - |
| dc.identifier.citation | Gonzalez, M., Romero, D., Zapata, B., & Betancur-Galvis, L. (2009). First synthesis of lissoclimide-type alkaloids. Letters in organic chemistry, 6(4), 289–292. https://doi.org/10.2174/157017809788489828 | spa |
| dc.identifier.issn | 1570-1786 | - |
| dc.identifier.uri | https://hdl.handle.net/10495/43565 | - |
| dc.description.abstract | ABSTRACT: The first synthesis of lissoclimide-type alkaloids is described. Starting from commercial (+)-sclareolide, the al-dehyde-bicyclohomofarnesal is synthesized and coupled, through an aldol reaction, with succinimide. The antitumor activity of several lissoclimide analogues is also reported. | spa |
| dc.format.extent | 4 páginas | spa |
| dc.format.mimetype | application/pdf | spa |
| dc.language.iso | eng | spa |
| dc.publisher | Bentham Science Publishers | spa |
| dc.type.hasversion | info:eu-repo/semantics/publishedVersion | spa |
| dc.rights | info:eu-repo/semantics/openAccess | spa |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/2.5/co/ | * |
| dc.title | First Synthesis of Lissoclimide-Type Alkaloids | spa |
| dc.type | info:eu-repo/semantics/article | spa |
| dc.publisher.group | GRID - Grupo de Investigación Dermatológica | spa |
| dc.publisher.group | Infección y Cáncer | spa |
| dc.identifier.doi | 10.2174/157017809788489828 | - |
| oaire.version | http://purl.org/coar/version/c_970fb48d4fbd8a85 | spa |
| dc.rights.accessrights | http://purl.org/coar/access_right/c_abf2 | spa |
| dc.identifier.eissn | 1875-6255 | - |
| oaire.citationtitle | Letters in Organic Chemistry | spa |
| oaire.citationstartpage | 289 | spa |
| oaire.citationendpage | 292 | spa |
| oaire.citationvolume | 6 | spa |
| dc.rights.creativecommons | https://creativecommons.org/licenses/by-nc-nd/4.0/ | spa |
| oaire.fundername | Universidad de Antioquia | spa |
| oaire.fundername | Colombia. Ministerio de Ciencia, Tecnología e Innovación - MinCiencias | spa |
| dc.publisher.place | Sarja, Emiratos Árabes Unidos | spa |
| dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | spa |
| dc.type.redcol | https://purl.org/redcol/resource_type/ART | spa |
| dc.type.local | Artículo de investigación | spa |
| dc.subject.decs | Diterpenos | - |
| dc.subject.decs | Diterpenes | - |
| dc.subject.decs | Alcaloides | - |
| dc.subject.decs | Alkaloids | - |
| dc.subject.agrovoc | Citotoxicidad | - |
| dc.subject.agrovoc | Cytotoxicity | - |
| dc.subject.agrovocuri | http://aims.fao.org/aos/agrovoc/c_34251 | - |
| dc.description.researchgroupid | COL0050839 | spa |
| dc.description.researchgroupid | COL0012328 | spa |
| oaire.awardnumber | RC 432-2004 | spa |
| dc.subject.meshuri | https://id.nlm.nih.gov/mesh/D004224 | - |
| dc.subject.meshuri | https://id.nlm.nih.gov/mesh/D000470 | - |
| dc.relation.ispartofjournalabbrev | Lett. Org. Chem. | spa |
| oaire.funderidentifier.ror | RoR:03bp5hc83 | - |
| oaire.funderidentifier.ror | RoR:03fd5ne08 | - |
| Aparece en las colecciones: | Artículos de Revista en Ciencias Médicas | |
Ficheros en este ítem:
| Fichero | Descripción | Tamaño | Formato | |
|---|---|---|---|---|
| ZapataBibiana_2009_First_Synthesis_Lissoclimide.pdf | Artículo de investigación | 136.59 kB | Adobe PDF | Visualizar/Abrir |
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