dc.creator | Kaiser, CR | |
dc.creator | Rittner, R | |
dc.creator | Basso, EA | |
dc.date | 1997 | |
dc.date | SEP | |
dc.date | 2014-12-16T11:33:28Z | |
dc.date | 2015-11-26T17:53:58Z | |
dc.date | 2014-12-16T11:33:28Z | |
dc.date | 2015-11-26T17:53:58Z | |
dc.date.accessioned | 2018-03-29T00:37:35Z | |
dc.date.available | 2018-03-29T00:37:35Z | |
dc.identifier | Magnetic Resonance In Chemistry. John Wiley & Sons Ltd, v. 35, n. 9, n. 609, n. 613, 1997. | |
dc.identifier | 0749-1581 | |
dc.identifier | WOS:A1997XU79600010 | |
dc.identifier | 10.1002/(SICI)1097-458X(199709)35:9<609 | |
dc.identifier | http://www.repositorio.unicamp.br/jspui/handle/REPOSIP/74683 | |
dc.identifier | http://www.repositorio.unicamp.br/handle/REPOSIP/74683 | |
dc.identifier | http://repositorio.unicamp.br/jspui/handle/REPOSIP/74683 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1290670 | |
dc.description | The high-field H-1 NMR analysis of 3-substituted camphors with OH, OMe, SMe, NHMe, NMe2 and Me substituents at endo and exo positions, and also with an oxo substituent, is reported. The substituent-induced chemical shifts (SCS) obtained for these difunctional systems, including those from previous work on 3-halocamphors, were examined in view of multilinear correlations with steric and electronic parameters. The resultant data show a strong contribution from the electric field mechanism, principally for the protons closer to the substituent. Carbonyl group interference on the expected SCS for the alpha-proton is also observed, with less deshielding than those of substituted bornanes and norbornanes. (C) 1997 by John Wiley & Sons, Ltd. | |
dc.description | 35 | |
dc.description | 9 | |
dc.description | 609 | |
dc.description | 613 | |
dc.language | en | |
dc.publisher | John Wiley & Sons Ltd | |
dc.publisher | W Sussex | |
dc.publisher | Inglaterra | |
dc.relation | Magnetic Resonance In Chemistry | |
dc.relation | Magn. Reson. Chem. | |
dc.rights | fechado | |
dc.rights | http://olabout.wiley.com/WileyCDA/Section/id-406071.html | |
dc.source | Web of Science | |
dc.subject | H-1 NMR chemical shifts | |
dc.subject | substituent-induced chemical shifts | |
dc.subject | 3-substituted camphors | |
dc.subject | steric effects | |
dc.subject | electronic effects | |
dc.subject | 2-substituted Cyclohexanones | |
dc.subject | Nmr | |
dc.subject | Spectroscopy | |
dc.subject | Mechanisms | |
dc.subject | Parameters | |
dc.subject | Definition | |
dc.subject | Constants | |
dc.subject | Resonance | |
dc.subject | Bonds | |
dc.subject | Scs | |
dc.title | Substituent-induced H-1 chemical shifts of 3-substituted camphors | |
dc.type | Artículos de revistas | |