Abstract
Abstract Nickel(II) and cobalt(III) chelates of the Schiff bases derived from salicylaldehyde and dipeptides such as glycylglycine, glycylalanine and alanylglycine have newly been prepared. The reactivity of methylene or methine groups in the dipeptide moieties of those Schiff base chelates has been investigated on the basis of their PMR spectra in D2O. It has been confirmed that the methylene or methine protons of the N-terminal amino acid residue are more easily activated than those of the C-terminal amino acid residue.
Sign-in/Register to access full text options 
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.
