Abstract
AbstractNitranions of pyrrole, aromatic and heteroaromatic amines, carboxamides and pyridyl carbanions are generated by deprotonation either of NH or CH acids. The positive or negative displacements undergone by the 15N nucleus relative to the neutral precursor depend on whether a σ or π charge is increased. They are associated with the symmetry of the nitrogen orbital in which the electron pair is either generated or that to which it is delocalized.
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.
