Pregled bibliografske jedinice broj: 296227
Enantiomers and Barriers to Racemization of Chiral Heterocyclic Biaryls
Enantiomers and Barriers to Racemization of Chiral Heterocyclic Biaryls // 5th Meeting on Stereochemistry
Liblice, Češka Republika, 1990. (poster, nije recenziran, sažetak, znanstveni)
CROSBI ID: 296227 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Enantiomers and Barriers to Racemization of Chiral Heterocyclic Biaryls
Autori
Mintas, Mladen ; Mannschreck, Albrecht
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Skup
5th Meeting on Stereochemistry
Mjesto i datum
Liblice, Češka Republika, 17.04.1990. - 19.04.1990
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
kiralni heterolitički biarili
(heterolitic biaryls; enantiomers)
Sažetak
Separation of the enantiomers (M) and (P) of sterically hindered N-aryl- 2(lH)-quinolone (l)l and N-aryl-4-pyridones (2)-(4) was achieved by liquid chromatography on triacetylcellulose. The barriers to partial rotation about the C-N bond in (l)-(4) were determined by thermal racemization of enantiomers. In order to find the preferred pathway for interconversion of enantiomers, transition barriers and geometries of the energetically more favourable transition states were estimated using molecular mechanichs method. The calculated energies for restricted rotation about the C-N bond are in reasonable accord with the experimental findings, yielding the same increasing order of enerigies.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Profili:
Mladen Mintas
(autor)