Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/129477
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dc.contributor.authorKennington, Stuart C. D.-
dc.contributor.authorFerré, Laura-
dc.contributor.authorRomo Fernández, Juan Manuel-
dc.contributor.authorRomea, Pedro-
dc.contributor.authorUrpí Tubella, Fèlix-
dc.contributor.authorFont Bardia, Ma. Mercedes-
dc.date.accessioned2019-03-04T15:22:32Z-
dc.date.available2019-03-04T15:22:32Z-
dc.date.issued2017-06-15-
dc.identifier.issn0022-3263-
dc.identifier.urihttp://hdl.handle.net/2445/129477-
dc.description.abstractDirect nickel-catalyzed alkylation of chiral N-acyl-4-isopropyl-1,3-thiazolidine-2-thiones using a commercially available nickel(II) complex, (Me3P)2NiCl2, has been developed for tropylium and trityl tetrafluoroborate salts. The reaction provides a single diastereomer of the corresponding adducts in good to high yields, which, in turn, can be easily converted into a wide array of enantiomerically pure compounds that are difficult to obtain by other asymmetric procedures.-
dc.format.extent8 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherAmerican Chemical Society-
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1021/acs.joc.7b00657-
dc.relation.ispartofJournal of Organic Chemistry, 2017, vol. 82, num. 12, p. 6426-6433-
dc.relation.urihttps://doi.org/10.1021/acs.joc.7b00657-
dc.rights(c) American Chemical Society , 2017-
dc.subject.classificationCatàlisi-
dc.subject.classificationNíquel-
dc.subject.classificationQuiralitat-
dc.subject.otherCatalysis-
dc.subject.otherNickel-
dc.subject.otherChirality-
dc.titleDiastereoselective and catalytic α-alkylation of chiral N-acyl thiazolidinethiones with stable carbocationic salts-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec672779-
dc.date.updated2019-03-04T15:22:32Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Química Inorgànica i Orgànica)

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