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dc.contributor.authorPeña González, Javier 
dc.contributor.authorTalavera, Garazi
dc.contributor.authorWaldecker, Bernd
dc.contributor.authorAlcarazo, Manuel
dc.date.accessioned2025-09-02T10:47:22Z
dc.date.available2025-09-02T10:47:22Z
dc.date.issued2016
dc.identifier.citationJ. Peña, G. Talavera, B. Waldecker, M. Alcarazo, Chem. Eur. J. 2017, 23, 75.es_ES
dc.identifier.issn0947-6539
dc.identifier.urihttp://hdl.handle.net/10366/166912
dc.description.abstract[EN]The efficient synthesis of a series of alkynylthioimidazolium salts through reaction of organozinc compounds with dibromo(imidazolium)sulfuranes is reported. Addition of Grignard reagents to these new species provided a highly modular, clean, and scalable access to a broad variety of alkynyl sulfides in good-to-excellent yields. The utility of this protocol was showcased by the preparation of alkynyl sulfides, which are particularly difficult to obtain or simply unavailable through the existing methodologies. In addition, the synthetic method was extended to the preparation of alkynyl selenides.es_ES
dc.language.isoenges_ES
dc.publisherWileyes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAlkynylthioimidazolium Saltses_ES
dc.subjectAlkynyl Sulfideses_ES
dc.subjectElectrophilic Thioalkynylationes_ES
dc.subjectalkynyl selenideses_ES
dc.subjecthypervalentes_ES
dc.titleAlkynylthioimidazolium Salts: Efficient Reagents for the Synthesis of Alkynyl Sulfides by Electrophilic Thioalkynylationes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1002/chem.201604760es_ES
dc.identifier.doi10.1002/chem.201604760
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn1521-3765
dc.journal.titleChemistry – A European Journales_ES
dc.volume.number23es_ES
dc.issue.number1es_ES
dc.page.initial75es_ES
dc.page.final78es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivatives 4.0 Internacional