Copper(I) selenophene-2-carboxylate (CuSC) promoted C–S cross-coupling reaction of thiols with aryl iodides

dc.creatorBarros, Olga Soares do Rêgo
dc.creatorSilva, Francielle Rodrigues da
dc.creatorNunes, Vanessa Lóren
dc.date.accessioned2024-07-18T14:20:50Z
dc.date.available2024-07-18T14:20:50Z
dc.date.issued2019
dc.description.abstractWe reported the synthesis of copper (I)-selenophene-2-carboxylate (CuSC) and application as new catalyst in the cross-coupling reactions of thiols with aryl iodide to afford the corresponding unsymmetrical thioethers. The optimized reaction conditions were applied to thiols and aryl iodides having a wide range of functional groups, including electron rich and electron poor substrates. The chemoselectivity of the reaction with 4-iodobromobenzene and 2-aminothiophenol derivatives was briefly examined through the competitive iodine versus bromine and thiol versus nitrogen cross-coupling.
dc.identifier.citationBARROS, Olga Soares do Rêgo; SILVA, Francielle Rodrigues; NUNES, Vanessa Loren. Copper(I) selenophene-2-carboxylate (CuSC) promoted C-S cross-coupling reaction of thiols with aryl iodides. Journal of Sulfur Chemistry, London, v. 40, n. 1, p. 9-17, 2019. DOI: 10.1080/17415993.2018.1519566. Disponível em: https://www.tandfonline.com/doi/full/10.1080/17415993.2018.1519566. Acesso em: 05 jul. 2024.
dc.identifier.doi10.1080/17415993.2018.1519566
dc.identifier.issne- 1741-6000
dc.identifier.issn1741-5993
dc.identifier.urihttps://www.tandfonline.com/doi/full/10.1080/17415993.2018.1519566
dc.language.isoeng
dc.publisher.countryGra-bretanha
dc.publisher.departmentInstituto de Química - IQ (RMG)
dc.rightsAcesso Restrito
dc.subjectUnsymmetrical thioethers
dc.subjectCopper(I) carboxylate
dc.subjectCrosscoupling
dc.subjectChemoselectivity
dc.subjectRegioselectivity
dc.titleCopper(I) selenophene-2-carboxylate (CuSC) promoted C–S cross-coupling reaction of thiols with aryl iodides
dc.typeArtigo

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