Abstract

1. A series of N-(2-hydroxyethyl) alkylidenamines (HEA) was produced by the condensation of ethanolamine with ketones. 2. The frequency of the C=N valence vibration in the IR spectra of HEA depends little on the electronic structure of C, N-substituents. 3. According to the data of the PMR spectra, HEA exists in two configurations (syn- and anti-isomers). 4. The polarographic reduction of HEA was studied; a dependence of the half-wave potential on the existence of an intramolecular hydrogen bond is observed.

Full Text
Paper version not known

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 call

Disclaimer: 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.