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http://hdl.handle.net/10261/115944
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Campo DC | Valor | Lengua/Idioma |
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dc.contributor.author | Bernal-Albert, Paloma | - |
dc.contributor.author | Faustino, Helio | - |
dc.contributor.author | Gimeno, Ana | - |
dc.contributor.author | Asensio, Gregorio | - |
dc.contributor.author | Mascareñas, José L. | - |
dc.contributor.author | López, Fernando | - |
dc.date.accessioned | 2015-06-01T08:26:14Z | - |
dc.date.available | 2015-06-01T08:26:14Z | - |
dc.date.issued | 2014 | - |
dc.identifier | doi: 10.1021/ol503121q | - |
dc.identifier | issn: 1523-7060 | - |
dc.identifier | e-issn: 1523-7052 | - |
dc.identifier.citation | Organic Letters 16: 6196-6199 (2014) | - |
dc.identifier.uri | http://hdl.handle.net/10261/115944 | - |
dc.description.abstract | α,β-Unsaturated N,N-dialkyl hydrazones undergo a mild [2 + 2] cycloaddition to allenamides when treated with a suitable gold catalyst. The method, which represents the first application of N,N-dialkyl hydrazones in gold catalysis, is compatible with a wide variety of substituents at the alkenyl moiety of the hydrazone component, proceeds with excellent levels of regio- and diastereoselectivity, and provides densely substituted cyclobutanes with good to excellent yields. | - |
dc.publisher | American Chemical Society | - |
dc.rights | closedAccess | - |
dc.title | Gold(I)-catalyzed intermolecular cycloaddition of allenamides with α,β-unsaturated hydrazones: Efficient access to highly substituted cyclobutanes | - |
dc.type | artículo | - |
dc.identifier.doi | 10.1021/ol503121q | - |
dc.date.updated | 2015-06-01T08:26:14Z | - |
dc.description.version | Peer Reviewed | - |
dc.language.rfc3066 | eng | - |
dc.identifier.pmid | 25406491 | - |
dc.type.coar | http://purl.org/coar/resource_type/c_6501 | es_ES |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.fulltext | No Fulltext | - |
item.cerifentitytype | Publications | - |
item.openairetype | artículo | - |
item.grantfulltext | none | - |
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