Mass Spectrometry of Some Benzylidene Imidazolidinediones and Thiazolidinediones. II- chlorobenzyl imidazolidinedione and Fluoro or Chlorobenzyl Thiazolidinedione Compounds

In the present investigation, a study of the electron impact mass spectrometry data is reported for seven compounds of a series of some 3-(4-chlorobenzyl)-5-benzylidene-imidazolidine-2, 4-diones and 3-(4-fluoro or chlorobenzyl)-5-benzylidene-thiazolidine-2, 4-diones previously synthesized.     

Structural and Stereochemical Analysis of Some 9-Phenyl-8-N-substituted Thiocarbamoyl-7,8-Diazabicyclo [4.3.0]non-6-enes by NMR and Mass Spectrometric Techniques

In this study the structural and stereo chemical analysis of some 9-Phenyl-8-N-Substituted thiocarbamoyl-7,8-diazabicyclo[4.-3.0] and the new synthesized 5-Methyl–9-phenyl-8-N-Substituted-thiocarbamoyl-7, 8-diazabicyclo[4.-3.0]non-6-enes derivatives were studied by 2D NMR, 1D NOE experiments and electron impact mass spectrometry were reported. The N-substituted thiocarbamoyl compounds were mixtures of diastereomers as evidenced by differing Rf values on TLC plates. They were separated by successive applications of preparative TLC and structures were elucidated by IR, ¹R-NMR, ¹³C-NMR, DEPT, 2D-NMR and EI-MASS techniques. The is-trans isomerism of the compounds were determined by means of ¹H-NMR, ¹³C-NMR and 1D NOE difference experiments. The conformation analysis of the bicyclic ring system was based on NOE difference experiments and NOESY spectra of compound-11. For the application of 1D NOE experiments, compound 11 was selected.