Abstract
Abstract The diastereoisomers of the ethyl-2,2,2-trichloroethyl diester of optically active 1-amino-1-phenylmethanephosphonic acid derivatives were examined by 1H NMR and IR methods. The configuration of the phosphorus atom in each diastereoisomer was determined on the basis of conformational analysis using 1H NMR spectra. Calculations of the location of the methylene protons in the trichloroethyl group as a function of dihedral angles were performed and compared with the experimental values.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
