Catching Elusive 2-Furyl Carbenes with Silanes: A Metal-Free Microwave-Assisted Silicon-Hydrogen Bond Functionalization

Título

dc.contributor.author	López García, Luis Ángel
dc.contributor.author	González-Pelayo, Silvia
dc.date.accessioned	2024-01-25T10:39:32Z
dc.date.available	2024-01-25T10:39:32Z
dc.date.issued	2016
dc.identifier.issn	1615-4150
dc.identifier.uri	http://hdl.handle.net/10366/154718
dc.description.abstract	An 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.iso	eng	es_ES
dc.subject	carbenesfuransmetal-free coinditionsmicrowave-assisted reactionsilanes	es_ES
dc.title	Catching Elusive 2-Furyl Carbenes with Silanes: A Metal-Free Microwave-Assisted Silicon-Hydrogen Bond Functionalization	es_ES
dc.type	info:eu-repo/semantics/article	es_ES
dc.relation.projectID	CTQ2013-41511-P	es_ES
dc.relation.projectID	GRUPIN14-013	es_ES
dc.rights.accessRights	info:eu-repo/semantics/openAccess	es_ES