z-logo
Premium
1 H and 13 C NMR studies of some O ‐carbamoyloximes
Author(s) -
Wazeer Mohammed I. M.,
Ali Sk. A.,
Arab Mohammed
Publication year - 1989
Publication title -
magnetic resonance in chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0749-1581
DOI - 10.1002/mrc.1260271117
Subject(s) - chemistry , benzaldehyde , substituent , nmr spectra database , spectral line , carbon 13 nmr , chemical shift , stereochemistry , computational chemistry , medicinal chemistry , organic chemistry , catalysis , physics , astronomy
The 1 H and 13 C NMR spectra were assigned for a series of O ‐carbamoyloximes of ortho ‐ and para ‐substituted benzaldehyde. These compounds exist exclusively in the E configuration. The aromatic protons and carbons show correlations with the appropriate substituent‐induced shifts and with Hammett parameters.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here