TY  - JOUR
A1  - Kleinpeter, Erich
A1  - Csütörtöki, Renáta
A1  - Szatmári, István
A1  - Heydenreich, Matthias
A1  - Koch, Andreas
A1  - Starke, Ines
A1  - Fulop, Ferenc
T1  - Novel piperidine-fused benzoxazino- and quinazolinonaphthoxazines-synthesis and conformational study
N2  - The reactions of 1-(amino(2-hydroxyphenyl)methyl)-2-naphthol (3) and 1-(amino(2-aminophenyl)methyl)-2-naphthol (6) with glutardialdehyde resulted in the formation of piperidine-fused benzoxazinonaphthoxazine 4 and quinazolinonaphthoxazine 7, respectively, both in diastereopure form. The full conformational search protocols of 4 and 7 were successfully carried out by NMR spectroscopy and accompanying molecular modelling; the global minimum-energy conformers of all diastereomers were computed, and the assignments of the most stable stereoisomers, Gtct1 for 4 and Gtct1 for 7, were corroborated by spatial NOE information relating to the H7a-H10a-H15b and H,H coupling patterns of the protons in the flexible part of the piperidine moiety. Additionally, mass spectrometric fragmentation was investigated in collision-induced dissociation experiments. The elemental compositions of the ions were determined by accurate mass measurements.
Y1  - 2012
UR  - https://publishup.uni-potsdam.de/frontdoor/index/index/docId/33292
SN  - 0040-4020
ER  -