Iodine(III)-Mediated Selective Intermolecular C-H Amination for the Chemical Diversification of Tryptamines

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Utilizad este identificador para citar o enlazar este documento: http://hdl.handle.net/2072/226309

dc.contributor.author	Bosnidou, Alexandra E.
dc.contributor.author	Millán, Alba
dc.contributor.author	Ceballos, Javier
dc.contributor.author	Martínez, Claudio
dc.contributor.author	Muñiz, Kilian
dc.date.accessioned	2018-01-15T16:04:10Z
dc.date.accessioned	2018-02-15T10:27:26Z
dc.date.available	2018-01-15T16:04:10Z
dc.date.available	2018-02-15T10:27:26Z
dc.date.issued	2016
dc.identifier.uri	http://hdl.handle.net/2072/226309
dc.identifier.uri	http://hdl.handle.net/2072/305743
dc.language.iso	eng
dc.publisher	ACS Publications
dc.relation	Ministerio de Economia y Competitivad
dc.relation	CTQ2011-25027 to K. M., and Severo Ochoa Excellence Accreditation 2014-2018 to ICIQ,
dc.relation.ispartof	JOC
dc.rights	American Chemical Society
dc.title	Iodine(III)-Mediated Selective Intermolecular C-H Amination for the Chemical Diversification of Tryptamines
dc.type	info:eu-repo/semantics/article
dc.relation.projectID	CTQ2014-56474R
dc.relation.projectID	SEV-2013-0319
dc.identifier.doi	https://dx.doi.org/10.1021/acs.joc.6b01118
dc.rights.accessLevel	info:eu-repo/semantics/openAccess
dc.description.abstract	Defined hypervalent iodine reagents of the general structure PhI[N(SO₂R)SO₂R’)]₂ promote the selective direct C-H-amination of the indole core of various tryptamines. Starting from a general C2-amination strategy, subsequent transformations enable a variety of site-selective functionalizations, which proceed with noteworthy high chemoselectivity and provide an overall access to structurally diversified products.

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