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dc.contributor.authorGarcía Bartolomé, Nuria 
dc.contributor.authorGarcía García, Patricia
dc.contributor.authorFernández Rodríguez, Manuel A. 
dc.contributor.authorRubio Presa, Rubén 
dc.contributor.authorPedrosa Sáez, María de los Remedios 
dc.contributor.authorArnáiz García, Francisco Javier 
dc.contributor.authorSanz Díez, Roberto 
dc.date.accessioned2015-12-01T12:35:17Z
dc.date.available2015-12-01T12:35:17Z
dc.date.issued2012-02
dc.identifier.issn1615-4150
dc.identifier.urihttp://hdl.handle.net/10259/3890
dc.description.abstractPinacol is disclosed as a new chemoselective and environmentally benign reducing agent for sulfoxides and nitroaromatics assisted by readily available dichlorodioxomolybdenum(VI) complexes as catalysts. A wide range of substrates including those bearing challenging functional groups has been efficiently and selectively reduced with acetone and water being the only by-products of these reactionsen
dc.description.sponsorshipMinisterio de Ciencia e Innovacion (MICINN) and FEDER (CTQ2010-15358 and CTQ2009-09949/BQU) and Junta de Castilla y Leon (BU021 A09 and GR-172) for financial support. P.G.-G. and M.A.F.-R. thank MICINN for "Juan de la Cierva" and "Ramon y Cajal" contractsen
dc.format.mimetypeapplication/pdf
dc.language.isoenges
dc.publisherWiley-VCH Verlagen
dc.relation.ispartofAdvanced Synthesis & Catalysis. 2012, V. 354, n. 2-3, p. 321–327en
dc.subjectchemoselectivityen
dc.subjectmolybdenumen
dc.subjectnitro compoundsen
dc.subjectreductionen
dc.subjectsulfoxidesen
dc.subject.otherQuímica orgánicaes
dc.titlePinacol as a new green reducing agent: molybdenum-catalyzed chemoselective reduction of sulfoxides and nitroaromaticsen
dc.typeArtículoes
dc.typeinfo:eu-repo/semantics/article
dc.description.versionThis is the peer reviewed version of the following article:García, N., García-García, P., Fernández-Rodríguez, M. A., Rubio, R., Pedrosa, M. R., Arnáiz, F. J. and Sanz, R. (2012), Pinacol as a New Green Reducing Agent: Molybdenum- Catalyzed Chemoselective Reduction of Sulfoxides and Nitroaromatics. Adv. Synth. Catal., 354: 321–327. doi: 10.1002/adsc.201100877 , which has been published in final form at 10.1002/adsc.201100877. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.relation.publisherversionhttp://dx.doi.org/10.1002/adsc.201100877
dc.identifier.doi10.1002/adsc.201100877
dc.subject.unescoChemistry, Organicen
dc.relation.projectIDinfo:eu-repo/grantAgreement/MICINN/CTQ2010-15358
dc.relation.projectIDinfo:eu-repo/grantAgreement/MICINN/CTQ2009-09949/BQU
dc.relation.projectIDinfo:eu-repo/grantAgreement/JCyL/BU021 A09
dc.relation.projectIDinfo:eu-repo/grantAgreement/JCyL/GR-172
dc.type.hasVersioninfo:eu-repo/semantics/acceptedVersionen


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