On the Aromatic Stability of Positional Isomers Consisting of Bicyclic Systems Composed Entirely of Five-Membered Heterocycles
M. Milun
; Ruder Boskovic Institute, p .O.B. 1016, 41000 Zagreb, Croatia, Yugoslavia
N. Trinajstić
; Ruder Boskovic Institute, p .O.B. 1016, 41000 Zagreb, Croatia, Yugoslavia
APA 6th Edition Milun, M. i Trinajstić, N. (1977). On the Aromatic Stability of Positional Isomers Consisting of Bicyclic Systems Composed Entirely of Five-Membered Heterocycles. Croatica Chemica Acta, 49 (1), 107-113. Preuzeto s https://hrcak.srce.hr/196421
MLA 8th Edition Milun, M. i N. Trinajstić. "On the Aromatic Stability of Positional Isomers Consisting of Bicyclic Systems Composed Entirely of Five-Membered Heterocycles." Croatica Chemica Acta, vol. 49, br. 1, 1977, str. 107-113. https://hrcak.srce.hr/196421. Citirano 08.03.2021.
Chicago 17th Edition Milun, M. i N. Trinajstić. "On the Aromatic Stability of Positional Isomers Consisting of Bicyclic Systems Composed Entirely of Five-Membered Heterocycles." Croatica Chemica Acta 49, br. 1 (1977): 107-113. https://hrcak.srce.hr/196421
Harvard Milun, M., i Trinajstić, N. (1977). 'On the Aromatic Stability of Positional Isomers Consisting of Bicyclic Systems Composed Entirely of Five-Membered Heterocycles', Croatica Chemica Acta, 49(1), str. 107-113. Preuzeto s: https://hrcak.srce.hr/196421 (Datum pristupa: 08.03.2021.)
Vancouver Milun M, Trinajstić N. On the Aromatic Stability of Positional Isomers Consisting of Bicyclic Systems Composed Entirely of Five-Membered Heterocycles. Croatica Chemica Acta [Internet]. 1977 [pristupljeno 08.03.2021.];49(1):107-113. Dostupno na: https://hrcak.srce.hr/196421
IEEE M. Milun i N. Trinajstić, "On the Aromatic Stability of Positional Isomers Consisting of Bicyclic Systems Composed Entirely of Five-Membered Heterocycles", Croatica Chemica Acta, vol.49, br. 1, str. 107-113, 1977. [Online]. Dostupno na: https://hrcak.srce.hr/196421. [Citirano: 08.03.2021.]
Sažetak Isomeric bicyclic conjugated systems consisting entirely of
five-membered heterocycles were studied using a novel aromaticity
index named topological resonance energy (TRE). TRE has correctly
predicted the aromatic behaviour of all the groups of isomers
studied. (These isomers called positional isomers because they
formally differ only by the position of a-bivalent heteroatoms)
may be classified into a particular group according their annelation
mode, which closely parallels TRE predictions and experimental
findings.