Substituent-induced C-13 chemical shifts of 3-substituted camphors

dc.creatorKaiser, CR
dc.creatorBasso, EA
dc.creatorRittner, R
dc.date2001
dc.dateOCT
dc.date2014-11-14T09:57:24Z
dc.date2015-11-26T17:14:24Z
dc.date2014-11-14T09:57:24Z
dc.date2015-11-26T17:14:24Z
dc.date.accessioned2018-03-29T00:02:43Z
dc.date.available2018-03-29T00:02:43Z
dc.identifierMagnetic Resonance In Chemistry. John Wiley & Sons Ltd, v. 39, n. 10, n. 643, n. 644, 2001.
dc.identifier0749-1581
dc.identifierWOS:000171233300015
dc.identifier10.1002/mrc.875
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/74682
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/74682
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/74682
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1281802
dc.descriptionThe complete C-13 NMR analysis of 3-substituted camphors with F, Cl, Br, I, OH, OMe, SMe, NHMe, NMe2 and Me substituents at endo and exo positions, and also the corresponding 'oxo' and dichloro derivatives, were obtained by 1D and 2D NMR techniques. The resulting substituent-induced chemical shifts (SCS) for these difunctional systems show the influence of electronic and steric mechanisms. Copyright (C) 2001 John Wiley & Sons, Ltd.
dc.description39
dc.description10
dc.description643
dc.description644
dc.languageen
dc.publisherJohn Wiley & Sons Ltd
dc.publisherW Sussex
dc.publisherInglaterra
dc.relationMagnetic Resonance In Chemistry
dc.relationMagn. Reson. Chem.
dc.rightsfechado
dc.rightshttp://olabout.wiley.com/WileyCDA/Section/id-406071.html
dc.sourceWeb of Science
dc.subjectNMR
dc.subjectC-13 NMR
dc.subject2D NMR
dc.subjectsubstituent-induced chemical shifts
dc.subject3-substituted camphors
dc.subjectelectronic effects
dc.subjectsteric effects
dc.subjectResonance
dc.titleSubstituent-induced C-13 chemical shifts of 3-substituted camphors
dc.typeArtículos de revistas


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