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| Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE | |
| Campo DC | Valor | Lengua/Idioma |
|---|---|---|
| dc.contributor.author | Gómez, Ana M. | - |
| dc.contributor.author | Lobo, Fernando | - |
| dc.contributor.author | Pérez De Las Vacas, Daniel | - |
| dc.contributor.author | Valverde, Serafín | - |
| dc.contributor.author | López, J. Cristóbal | - |
| dc.date.accessioned | 2013-11-06T10:12:21Z | - |
| dc.date.available | 2013-11-06T10:12:21Z | - |
| dc.date.issued | 2010 | - |
| dc.identifier | doi: 10.1039/c0cc00586j | - |
| dc.identifier | issn: 1359-7345 | - |
| dc.identifier | e-issn: 1364-548X | - |
| dc.identifier.citation | Chemical Communications 46: 6159- 6161 (2010) | - |
| dc.identifier.uri | http://hdl.handle.net/10261/85648 | - |
| dc.description.abstract | Pyranosidic allylic (Ferrier) cations that share dicobalt hexacarbonyl propargyl (Nicholas) stabilization at C-1 display a remarkable reactivity leading to either substituted oxepanes or 3-C-branched pyranosides, depending on the substituent at O-6. © 2010 The Royal Society of Chemistry. | - |
| dc.language.iso | eng | - |
| dc.publisher | Royal Society of Chemistry (UK) | - |
| dc.rights | closedAccess | - |
| dc.title | Formation and reactivity of new Nicholas-Ferrier pyranosidic cations: Novel access to oxepanes via a 1,6-hydride shift/cyclization sequence | - |
| dc.type | artículo | - |
| dc.identifier.doi | 10.1039/c0cc00586j | - |
| dc.date.updated | 2013-11-06T10:12:21Z | - |
| dc.description.version | Peer Reviewed | - |
| dc.type.coar | http://purl.org/coar/resource_type/c_6501 | es_ES |
| item.openairetype | artículo | - |
| item.grantfulltext | none | - |
| item.cerifentitytype | Publications | - |
| item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
| item.fulltext | No Fulltext | - |
| item.languageiso639-1 | en | - |
| Aparece en las colecciones: | (IQOG) Artículos | |
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| Fichero | Descripción | Tamaño | Formato | |
|---|---|---|---|---|
| accesoRestringido.pdf | 15,38 kB | Adobe PDF |  Visualizar/Abrir |
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