Palladium-Catalyzed Direct C-H Arylation of 3-(Methylsulfinyl)thiophenes

dc.creatorJiang, Hui
dc.creatorBellomo Peraza, Ana Ines
dc.creatorZhang, Mengnan
dc.creatorCarroll, Patrick J.
dc.creatorManor, Brian C.
dc.creatorJia, Tiezheng
dc.creatorWalsh, Patrick J.
dc.date.accessioned2020-03-06T19:58:20Z
dc.date.accessioned2022-10-15T02:49:49Z
dc.date.available2020-03-06T19:58:20Z
dc.date.available2022-10-15T02:49:49Z
dc.date.created2020-03-06T19:58:20Z
dc.date.issued2018-05
dc.identifierJiang, Hui; Bellomo Peraza, Ana Ines; Zhang, Mengnan; Carroll, Patrick J.; Manor, Brian C.; et al.; Palladium-Catalyzed Direct C-H Arylation of 3-(Methylsulfinyl)thiophenes; American Chemical Society; Organic Letters; 20; 9; 5-2018; 2522-2525
dc.identifier1523-7060
dc.identifierhttp://hdl.handle.net/11336/98977
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4336977
dc.description.abstractA palladium-catalyzed direct arylation of (3-thiophene)S(O)Me derivatives has been developed. This protocol is effective for the selective synthesis of 2-arylated and 2,5-diarylated sulfinylthiophene derivatives with as low as 0.5 mol % catalyst loading. Various functional groups are well tolerated. A method to install two different aryl groups on 3-(methylsulfinyl)thiophenes is also introduced.
dc.languageeng
dc.publisherAmerican Chemical Society
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1021/acs.orglett.8b00599
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/acs.orglett.8b00599
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectDIRECT ARYLATION
dc.subjectHIGH THROUGHPUT SCREENING
dc.subjectSULFINYL THIOPHENES
dc.titlePalladium-Catalyzed Direct C-H Arylation of 3-(Methylsulfinyl)thiophenes
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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