1H N.M.R. spectra of some 5-substituted-3-isopropyl-6-methyl uracils
Само за регистроване кориснике
1988
Чланак у часопису (Објављена верзија)
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The 1H n.m.r. spectra of some 5-substituted-3-isopropyl-6-methyl uracils were determined in deuterated dimethyl sulfoxide (d6-DMSO). The substituents are: H, Cl, Br, I, NO2, NH2, N(CH3)2, C6H5, C6H4-NO2-p and C6H4-NH2-p. It has been shown that relative chemical shift (Δδ) of N(1)-H proton of some of the examined compounds correlated linearly with Hammett σm constant for the substituents in position 5 of uracil ring. The correlation with the σm constant was interpreted as providing evidence that the inductive effect of the substituent on chemical shift is dominating one.
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Journal of Molecular Structure, 1988, 174, C, 281-284Институција/група
Poljoprivredni fakultetTY - JOUR AU - Jovanović, B.Z. AU - Tadić, Z.D. AU - Muškatirović, M.D. AU - Pešić, Mirjana AU - Bogdanović, S.I. PY - 1988 UR - http://aspace.agrif.bg.ac.rs/handle/123456789/65 AB - The 1H n.m.r. spectra of some 5-substituted-3-isopropyl-6-methyl uracils were determined in deuterated dimethyl sulfoxide (d6-DMSO). The substituents are: H, Cl, Br, I, NO2, NH2, N(CH3)2, C6H5, C6H4-NO2-p and C6H4-NH2-p. It has been shown that relative chemical shift (Δδ) of N(1)-H proton of some of the examined compounds correlated linearly with Hammett σm constant for the substituents in position 5 of uracil ring. The correlation with the σm constant was interpreted as providing evidence that the inductive effect of the substituent on chemical shift is dominating one. T2 - Journal of Molecular Structure T1 - 1H N.M.R. spectra of some 5-substituted-3-isopropyl-6-methyl uracils EP - 284 IS - C SP - 281 VL - 174 DO - 10.1016/0022-2860(88)80171-6 ER -
@article{ author = "Jovanović, B.Z. and Tadić, Z.D. and Muškatirović, M.D. and Pešić, Mirjana and Bogdanović, S.I.", year = "1988", abstract = "The 1H n.m.r. spectra of some 5-substituted-3-isopropyl-6-methyl uracils were determined in deuterated dimethyl sulfoxide (d6-DMSO). The substituents are: H, Cl, Br, I, NO2, NH2, N(CH3)2, C6H5, C6H4-NO2-p and C6H4-NH2-p. It has been shown that relative chemical shift (Δδ) of N(1)-H proton of some of the examined compounds correlated linearly with Hammett σm constant for the substituents in position 5 of uracil ring. The correlation with the σm constant was interpreted as providing evidence that the inductive effect of the substituent on chemical shift is dominating one.", journal = "Journal of Molecular Structure", title = "1H N.M.R. spectra of some 5-substituted-3-isopropyl-6-methyl uracils", pages = "284-281", number = "C", volume = "174", doi = "10.1016/0022-2860(88)80171-6" }
Jovanović, B.Z., Tadić, Z.D., Muškatirović, M.D., Pešić, M.,& Bogdanović, S.I.. (1988). 1H N.M.R. spectra of some 5-substituted-3-isopropyl-6-methyl uracils. in Journal of Molecular Structure, 174(C), 281-284. https://doi.org/10.1016/0022-2860(88)80171-6
Jovanović B, Tadić Z, Muškatirović M, Pešić M, Bogdanović S. 1H N.M.R. spectra of some 5-substituted-3-isopropyl-6-methyl uracils. in Journal of Molecular Structure. 1988;174(C):281-284. doi:10.1016/0022-2860(88)80171-6 .
Jovanović, B.Z., Tadić, Z.D., Muškatirović, M.D., Pešić, Mirjana, Bogdanović, S.I., "1H N.M.R. spectra of some 5-substituted-3-isopropyl-6-methyl uracils" in Journal of Molecular Structure, 174, no. C (1988):281-284, https://doi.org/10.1016/0022-2860(88)80171-6 . .