STEREOSPECIFICITY OF SHIELDING CONSTANTS OF CARBON-13 NUCLEI IN <sup>13</sup>C NMR SPECTRA OF OXIMES OF HETARENECARBALDEHYDES AND ALKYL HETERYL KETONES
DOI:
https://doi.org/10.1007/7214Keywords:
оксимы с гетероциклическими заместителями, спектры ЯМР 13С, стереоспецифичность констант экранированияAbstract
It has been discovered that the chemical shifts of carbon atoms in 13C NMR spectra of oximes having pyrrolyl, furyl, benzofuryl, thienyl, and pyridyl rings as substituents are changed systematically on
going from the E- to the Z-isomer. This makes it possible to use the indicated chemical shifts for establishing the configuration of oximes with heterocyclic substituents and studying the special features of their electronic structure.
How to Cite
Afonin, A. V.; Ushakov, I. A.; Simonenko, D. E.; Schmidt, E. Yu.;
Zorina, N. V.; Ivanov, A. V.; Vasil'tsov, A. M.; Mikhaleva, A. I. Chem. Heterocycl. Compd. 2008, 44, 1238. [Khim. Geterotsikl. Soedin. 2008, 1523.]
For this article in the English edition see DOI 10.1007/s10593-009-0172-3