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dc.contributor.authorLópez García, Luis Ángel
dc.contributor.authorGonzález-Pelayo, Silvia
dc.date.accessioned2024-01-25T10:39:32Z
dc.date.available2024-01-25T10:39:32Z
dc.date.issued2016
dc.identifier.issn1615-4150
dc.identifier.urihttp://hdl.handle.net/10366/154718
dc.description.abstractAn efficient, metal-free, silicon-hydrogen bond functionalization based on the microwave-assisted reaction of readily available enynones and silanes is reported. This process seemingly proceeds through a 2-furyl carbene species, a particularly elusive intermediate. Preliminary studies on the metal-free oxygen-hydrogen and nitrogen-hydrogen bond functionalization of representative alcohols, azoles and sulfonamides are also provided.es_ES
dc.language.isoenges_ES
dc.subjectcarbenesfuransmetal-free coinditionsmicrowave-assisted reactionsilaneses_ES
dc.titleCatching Elusive 2-Furyl Carbenes with Silanes: A Metal-Free Microwave-Assisted Silicon-Hydrogen Bond Functionalizationes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.projectIDCTQ2013-41511-Pes_ES
dc.relation.projectIDGRUPIN14-013es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES


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