The effect of electron-withdrawing groups on15N and13C chemical shifts: a density functional study on a series of pyrroles
Author:
Publisher
Informa UK Limited
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics,Molecular Biology,Biophysics
Link
http://www.tandfonline.com/doi/pdf/10.1080/00268970412331333519
Reference35 articles.
1. X-ray Crystallographic and 13C NMR Investigations of the Effects of Electron-Withdrawing Groups on a Series of Pyrroles
2. Synthesis and Properties of Ring-Deactivated Deuterated (Hydroxymethyl)pyrroles
3. Efficient synthesis of (±)-N-BOC-exo-2-(methoxycarbonyl)-7-Azabicyclo[2.2.1]heptane, a versatile intermediate for the synthesis of epibatidine and epiboxidine
4. A versatile total synthesis of epibatidine and analogs
5. Synthesis of (.+-.)-ferruginine and (.+-.)-anhydroecgonine methyl-ester by a tandem cyclopropanation/Cope rearrangement
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1. Pyrroles and Their Benzo Derivatives: Structure;Comprehensive Heterocyclic Chemistry IV;2022
2. Experimental and theoretical characterization of a novel bis-pyrazoylmethane ligand;Magnetic Resonance in Chemistry;2015-04-27
3. Aromaticity and Aminopyrroles: Desmotropy and Solution Tautomerism of 1H-Pyrrol-3-aminium and 1H-Pyrrol-3(2H)-iminium Cation: A Stable σ-Complex;The Journal of Organic Chemistry;2013-01-10
4. References;Handbook of Heterocyclic Chemistry;2010
5. Measurement and calculation of 13C and 15N NMR chemical-shift tensors of a push–pull ethylene;Canadian Journal of Chemistry;2009-04
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