Additive of substituent effects on the chemical shift of the formyl proton in disubstituted benzaldehydes
An additivity relationship of substituent effects on the formyl proton chemical shift has been tested with ten disubstituted benzaldehydes. In most cases it is found that the formyl proton chemical shift, extrapolated to infinite dilution in nitromethane, is in good agreement with that calculated us...
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Formato: | Capítulo de libro |
Lenguaje: | Inglés |
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1980
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003 | AR-BaUEN | ||
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008 | 190411s1980 xx ||||fo|||| 00| 0 eng|d | ||
024 | 7 | |2 scopus |a 2-s2.0-84986769172 | |
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100 | 1 | |a Castañeda, H.O. | |
245 | 1 | 0 | |a Additive of substituent effects on the chemical shift of the formyl proton in disubstituted benzaldehydes |
260 | |c 1980 | ||
270 | 1 | 0 | |m Contreras, R.H.; Departamento de Física, Facultad de Ciencias Exactas Y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pabellón 1, Buenos Aires, 1428, Argentina |
504 | |a Contreras, R.H., de Kowalewski, D.G., Osella, A., Org. Magn. Reson. in press; Contreras, R.H., de Kowalewski, D.G., (1974) J. Mol. Struct., 23, p. 209 | ||
504 | |a Zanger, M., The determination of aromatic substitution patterns by nuclear magnetic resonance (1972) Organic Magnetic Resonance, 4, p. 1 | ||
504 | |a Beeby, J., Sternhell, S., Hoffmann‐Ostenhof, T., Pretsch, E., Simon, W., (1973) Anal. Chem., 45, p. 1571 | ||
504 | |a Batts, B.D., Pasaribu, S.J., Williams, L.R., The proton magnetic resonance spectra of some disubstituted acetophenones (1977) Organic Magnetic Resonance, 9, p. 210 | ||
504 | |a Hólik, M., Effect of substituents on the1H n.m.r. spectra ofpara-disubstituted benzenes. A graphical aid in the correct assignment of chemical shifts (1977) Organic Magnetic Resonance, 9, p. 491 | ||
504 | |a Kowalewski, V.J., (1969) J. Mol. Spectrosc., 30, p. 531 | ||
506 | |2 openaire |e Política editorial | ||
520 | 3 | |a An additivity relationship of substituent effects on the formyl proton chemical shift has been tested with ten disubstituted benzaldehydes. In most cases it is found that the formyl proton chemical shift, extrapolated to infinite dilution in nitromethane, is in good agreement with that calculated using the additivity relationship. Copyright © 1980 Heyden & Son Ltd. |l eng | |
593 | |a Departamento de Física, Facultad de Ciencias Exactas Y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pabellón 1, Buenos Aires, 1428, Argentina | ||
700 | 1 | |a Contreras, Rubén Horacio | |
700 | 1 | |a de Kowalewski, D.G. | |
773 | 0 | |d 1980 |g v. 13 |h pp. 308-309 |k n. 4 |p Magn. Reson. Chem. |x 00304921 |w (AR-BaUEN)CENRE-2295 |t Organic Magnetic Resonance | |
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961 | |a paper_00304921_v13_n4_p308_Castaneda |b paper |c PE | ||
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