作者:Janaína Marques Rodrigues、Carlos Mauricio R. Sant’Anna、Victor Marcos Rumjanek、João Batista Neves DaCosta                                    
                                    
                                        DOI:10.1080/10426500903444366
                                    
                                    
                                        日期:2009.12.29
                                    
                                    A series of 22 dialkylphosphorylydrazones (dialkyl ester, N'-[(1E)-(R(1) phenyl)methylene]-phosphorohydrazidic acid), 20 of them new, along with three new N,N'-bis(diisobutylphosphorylthioamide)diamines (bis-[diisobutyl ester), N-thioxomethylene]-, diamine)phosphoramidic acid, were prepared and characterized by IR, (1)H NMR, (13)C NMR, (31)P NMR, and mass spectrometry. The analysis of (1)H NMR, (13)C NMR, (31)P NMR, and NOE spectra confirmed the observation of the single diastereoisomer E in the synthesis of dialkylphosphorylydrazones. The results of a molecular modeling study performed in order to investigate the mechanism of the synthesis of dialkylphosphorylydrazones are in agreement with the experimental results, i.e., the favored formation of diastereoisomer E over Z.