Structural peculiarities of configurational isomers of 1-styrylpyrroles according to1Н,13С and15N NMR spectroscopy and density functional theory calculations: electronic and steric hindrance for planar structure-Reference-Cited by-同舟云学术

Structural peculiarities of configurational isomers of 1-styrylpyrroles according to1Н,13С and15N NMR spectroscopy and density functional theory calculations: electronic and steric hindrance for planar structure

Published:2013-04-04 Issue:6 Volume:51 Page:339-349
ISSN:0749-1581
Container-title:Magnetic Resonance in Chemistry
language:en
Short-container-title:Magn. Reson. Chem.

Author:

Afonin Andrei V.¹,Ushakov Igor A.¹,Pavlov Dmitry V.¹,Schmidt Elena Yu.¹,Dvorko Marina Yu.¹

Affiliation:

1. Institute of Chemistry; Siberian Branch of the Russian Academy of Science; Favorski St 1; 664033; Irkutsk; Russia

Publisher

Wiley

Subject

General Materials Science,General Chemistry

Reference40 articles.

1. 1H and 13C NMR spectra of N-vinylpyrroles

2. Pyrroles from ketoximes and acetylene. 11. Conformation of 1-vinylpyrroles from1H NMR data

3. Pyrroles from ketoximes and acetylene. 13. Study of some substituted pyrroles by13C NMR spectroscopy and calculations with the CNDO/2 approximation

4. 1H and 13C nmr study of conformational and electronic structure of 1-vinylpyrroles

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