Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/46043
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dc.contributor.authorCorominas, Albert (Corominas Tarruella)-
dc.contributor.authorMontaña Pedrero, Ángel-Manuel-
dc.date.accessioned2013-09-17T12:06:16Z-
dc.date.available2014-12-31T23:02:03Z-
dc.date.issued2013-
dc.identifier.issn0039-7911-
dc.identifier.urihttp://hdl.handle.net/2445/46043-
dc.description.abstractA method to generate carbonylic compounds from alkynes under mild and neutral conditions, with excellent functional group compatibility and high yields, is described. Hydration takes place under catalytic conditions by using from 0.1 to 0.2 equivalents of the easily available and inexpensive mercury(II) p-toluensulfonamidate in a hydroalcoholic solution. After use the catalyst is iner tized and/or recycled ...eng
dc.format.extent24 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoengeng
dc.publisherTaylor and Francis-
dc.relation.isformatofVersió postprint del document publicat a: http://dx.doi.org/10.1080/00397911.2012.686003-
dc.relation.ispartofSynthetic Communications, 2013, vol. 43, num. 15, p. 2062-2072-
dc.relation.urihttp://dx.doi.org/10.1080/00397911.2012.686003-
dc.rights(c) Taylor and Francis, 2013-
dc.sourceArticles publicats en revistes (Química Inorgànica i Orgànica)-
dc.subject.classificationCompostos carbonílicscat
dc.subject.classificationQuímica orgànicacat
dc.subject.otherCarbonyl compoundseng
dc.subject.otherOrganic chemistryeng
dc.titleVersatile methodology to hydrate alkynes, in the presence of a wide variety of functional groups, with Mercury(II) p-Toluensulfonamidate, under catalytic, mild and neutral conditions-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec623938-
dc.date.updated2013-09-17T10:44:22Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Química Inorgànica i Orgànica)

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