Configurations in unsymmetrically N-methyl-N-substituted 2-phenylacetamides
Само за регистроване кориснике
1986
Чланак у часопису (Објављена верзија)
,
Elsevier
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The syntheses of a various N-methyl-N-substituted 2-phenylacetamides of the general formula PhCH 2 CON(CH 3 )R, wherein, R is ethyl, n-propyl, isopropyl and t-butyl group, were performed. The 1 H n.m.r. spectra of these unsymetrically N,N-disubstituted amides have been studied and the peaks have been assigned in each case to the two possible conformational isomers, arising from the lack of free rotation about the C(O)N bond. Although the cis form predominates, the percentage of cis isomer increases as the other nitrogen substituent becomes more bulky. These results are in accordance with our previous investigation of the structures of N-monosubstituted 2-phenylacetamides. © 1986.
Извор:
Journal of Molecular Structure, 1986, 142, C, 451-453Издавач:
- Elsevier
Институција/група
IHTMTY - JOUR AU - Petrović, Slobodan D. AU - Vajs, Vlatka AU - Nikolić, Aleksandar D. AU - Stojanović, Nada D. PY - 1986 UR - https://cer.ihtm.bg.ac.rs/handle/123456789/2785 AB - The syntheses of a various N-methyl-N-substituted 2-phenylacetamides of the general formula PhCH 2 CON(CH 3 )R, wherein, R is ethyl, n-propyl, isopropyl and t-butyl group, were performed. The 1 H n.m.r. spectra of these unsymetrically N,N-disubstituted amides have been studied and the peaks have been assigned in each case to the two possible conformational isomers, arising from the lack of free rotation about the C(O)N bond. Although the cis form predominates, the percentage of cis isomer increases as the other nitrogen substituent becomes more bulky. These results are in accordance with our previous investigation of the structures of N-monosubstituted 2-phenylacetamides. © 1986. PB - Elsevier T2 - Journal of Molecular Structure T1 - Configurations in unsymmetrically N-methyl-N-substituted 2-phenylacetamides VL - 142 IS - C SP - 451 EP - 453 DO - 10.1016/0022-2860(86)85154-7 ER -
@article{ author = "Petrović, Slobodan D. and Vajs, Vlatka and Nikolić, Aleksandar D. and Stojanović, Nada D.", year = "1986", abstract = "The syntheses of a various N-methyl-N-substituted 2-phenylacetamides of the general formula PhCH 2 CON(CH 3 )R, wherein, R is ethyl, n-propyl, isopropyl and t-butyl group, were performed. The 1 H n.m.r. spectra of these unsymetrically N,N-disubstituted amides have been studied and the peaks have been assigned in each case to the two possible conformational isomers, arising from the lack of free rotation about the C(O)N bond. Although the cis form predominates, the percentage of cis isomer increases as the other nitrogen substituent becomes more bulky. These results are in accordance with our previous investigation of the structures of N-monosubstituted 2-phenylacetamides. © 1986.", publisher = "Elsevier", journal = "Journal of Molecular Structure", title = "Configurations in unsymmetrically N-methyl-N-substituted 2-phenylacetamides", volume = "142", number = "C", pages = "451-453", doi = "10.1016/0022-2860(86)85154-7" }
Petrović, S. D., Vajs, V., Nikolić, A. D.,& Stojanović, N. D.. (1986). Configurations in unsymmetrically N-methyl-N-substituted 2-phenylacetamides. in Journal of Molecular Structure Elsevier., 142(C), 451-453. https://doi.org/10.1016/0022-2860(86)85154-7
Petrović SD, Vajs V, Nikolić AD, Stojanović ND. Configurations in unsymmetrically N-methyl-N-substituted 2-phenylacetamides. in Journal of Molecular Structure. 1986;142(C):451-453. doi:10.1016/0022-2860(86)85154-7 .
Petrović, Slobodan D., Vajs, Vlatka, Nikolić, Aleksandar D., Stojanović, Nada D., "Configurations in unsymmetrically N-methyl-N-substituted 2-phenylacetamides" in Journal of Molecular Structure, 142, no. C (1986):451-453, https://doi.org/10.1016/0022-2860(86)85154-7 . .