Genc, HasanTan, MeltemGumus, SelcukMenges, NurettinBildirici, IshakSener, Ahmet2025-05-102025-05-1020100253-29641229-594910.5012/bkcs.2010.31.9.26332-s2.0-77957193857https://doi.org/10.5012/bkcs.2010.31.9.2633https://hdl.handle.net/20.500.14720/1689Bildirici, Ishak/0000-0001-8590-3070; Menges, Nurettin/0000-0002-5990-62753-Acety1-5-benzoy1-6-methy1-2-pheny1-4H-pyran-4-one has been subjected to condensation with a series of primary amines (ethylamine - octylamine) to clarify the proposed mechanism in our previous study. The reactions of the shorter amines of the series (ethylamine - butylamine) yielded unsymmetric pyridinone products, whereas the other amines (pentylamine - octylamine) yielded symmetrical pyridinones. The starting material and the products as well as the intermediates have been subjected to theoretical analysis by quantum chemical calculations at B3LYP/6-3 I G(d,p) level, which provided supporting data for the experimental findings.eninfo:eu-repo/semantics/openAccessHeterocyclic CompoundsPyranonesPyridinonesQuantum Chemical CalculationsArticle319Q3Q226332636WOS:000283953600037