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Experimental and Theoretical-Study of Carbon-Fluorine Couplings in the NMR-Spectra of 2-Fluoroaryl Ketones

RH Contreras, CG Giribet, MA Natiello, J Perez, ID Rae and JA Weigold
38(12) pp.1779 - 1784


18 articles found in Crossref database.

Analysis of unusual 13C77Se couplings in the 13C NMR spectra of selenoimidates
Contreras R. H., de Azúa M. C. Ruíz, Giribet C. G.
Magnetic Resonance in Chemistry. 1986 24(8). p.675
Fluorine deshielding in the proximity of a methyl group. An experimental and theoretical study
Gribble Gordon W., Keavy Daniel J., Olson Erik R., Rae Ian D., Staffa Alfred, Herr Tomas E., Ferraro Marta B., Contreras Rubén H.
Magnetic Resonance in Chemistry. 1991 29(5). p.422
Signs of 19F1H and 19F13C spin–spin coupling constants mainly transmitted through space
Rae I. D., Weigold J. A., Contreras R. H., Yamamoto G.
Magnetic Resonance in Chemistry. 1992 30(11). p.1047
Through‐space 13C–19F couplings in highly‐crowded systems: Radial dependence and electronic effects
Hsee Li C., Sardella D. J.
Magnetic Resonance in Chemistry. 1990 28(8). p.688
C–F Bonds as “Frozen” Nucleophiles: Unconsummated SN2 Reactions
Harry Stefan Andrew, Garrison Nathaniel G., Zhu Andrea, Xiang Michael Richard, Siegler Maxime A., Lectka Thomas
The Journal of Organic Chemistry. 2022 87(19). p.13406
Theoretical IPPP analysis of 13C‐31 P through‐space indirect couplings in phosphorus‐substituted alkenes
Diz A. C., Giribet C. G., de Azúa M. C. Ruiz, Contreras R. H., Aucar G. A.
Magnetic Resonance in Chemistry. 1987 25(10). p.883
The electronic origin of unusually large nJFN coupling constants in some fluoroximes
Favaro Denize C., Contreras Rubén H., Tormena Cláudio F.
Magnetic Resonance in Chemistry. 2013 51(6). p.334
Novel Synthesis, Reactivity, and Stereochemistry of Substituted 3-Trifluoromethyl- and 3-Perfluoroalkyl-3-phenoxyprop-2-enal
El Kharrat Salem, Laurent Philippe, Blancou Hubert
The Journal of Organic Chemistry. 2006 71(18). p.6742
(2003)
CONTRERAS RUBÉN H., BARONE VERÓNICA, FACELLI JULIO C., PERALTA JUAN E.
Truncated Aspidosperma Alkaloid-Like Scaffolds: Unique Structures for the Discovery of New, Bioactive Compounds
K. Snyder John, C. Benson Scott, Lee Lily, Wei Wanguo, Ni Feng, David Janna Olmos Julian, R. Strom Kyle, B. Beeler Aaron, Chih-Chien Cheng Ken, Inglese James, Kota Smitha, Takahashi Virginia, Donny Strosberg A., H. Connor John, Guy Bushkin G.
HETEROCYCLES. 2012 84(1). p.135
Indirect Nonbonded Nuclear Spin–Spin Coupling: A Guide for the Recognition and Understanding of “Through-Space” NMR J Constants in Small Organic, Organometallic, and Coordination Compounds
Hierso Jean-Cyrille
Chemical Reviews. 2014 114(9). p.4838
Analysis of 19F and 13C NMR spectra of tetrafluorophthalic anhydride and its derivatives
Chuikov Igor P., Fadeev Dmitriy S., Mamatyuk Victor I., Vaganova Tamara A., Malykhin Evgenij V.
Journal of Fluorine Chemistry. 2011 132(8). p.512
Viewpoint 8 — polarization propagator analysis of spin-spin coupling constants
Contreras R.H., de Azúa M.C.Ruiz, Giribet C.G., Aucar G.A., de Bonczok R.Lobayan
Journal of Molecular Structure: THEOCHEM. 1993 284(3). p.249
1H and13C spectra of fluorine‐containing polycyclic aromatic hydrocarbons.1H19F and13C19F coupling across bay regions
Sardella D. J., Boger E.
Magnetic Resonance in Chemistry. 1989 27(1). p.13
Analysis of long‐range through‐space couplings via an intramolecular hydrogen bond
Rae Ian D., Weigold Josephine A., Contreras Rubén H., Biekofsky Rodolfo R.
Magnetic Resonance in Chemistry. 1993 31(9). p.836
(1993)
Contreras R.H., Facelli J.C.
Spin—spin coupling constants between carbons separated by more than one bond
Krivdin Leonid B., Della Ernest W.
Progress in Nuclear Magnetic Resonance Spectroscopy. 1991 23(4-6). p.301
Conformational analysis of methyl phenyl sulphoxides containing fluorine substituents in the phenyl ring based on 1H, 13C and 17O NMR chemical shifts and long‐range nJ(HF) and nJ(CF) coupling constants
Benassi Rois, Folli Ugo, Iarossi Dario, Mucci Adele, Schenetti Luisa, Taddei Ferdinando
Magnetic Resonance in Chemistry. 1990 28(8). p.702

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