Structural studies on 9-hydrazono-6,7,8,9-tetrahydro-4-oxo-4H-pyrido[1,2-a]pyrimidines by1H,13C and15N NMR spectroscopy
                                
                                    
                                        作者:Gábor Tóth、ÁRon Szöllösy、Attila Almásy、Benjámin Podányi、István Hermecz、Tibor Breining、Zoltán Mészáros                                    
                                    
                                        DOI:10.1002/omr.1270211111
                                    
                                    
                                        日期:1983.11
                                    
                                    Abstract1H, 13C and 15N NMR studies demonstrated that 9‐hydrazono‐6,7,8,9‐tetrahydro‐4‐oxo‐4H‐pyrido‐[1,2‐a] pyrimidlnes exist as an equilibrium mixture of Z‐E isomers in the hydrazono–imino tautomeric form having an exocyclic double bond. Proton‐catalysed Z‐E interconversion is fast. Substituent and solvent effects revealed that the decisive factors controlling the Z:E ratio are internal hydrogen bonding in the Z‐isomer, stabilization by solvation and steric interaction.