Tautomerism of N-substituted acridin-9-amines in the context of dynamic NMR and matrix isolation-FT-IR spectroscopy supported by DFT calculations and structural analysis-Reference-Cited by-同舟云学术

Tautomerism of N-substituted acridin-9-amines in the context of dynamic NMR and matrix isolation-FT-IR spectroscopy supported by DFT calculations and structural analysis

Published:2020-10 Issue: Volume:1218 Page:128424
ISSN:0022-2860
Container-title:Journal of Molecular Structure
language:en
Short-container-title:Journal of Molecular Structure

Author:

Krzymiński Karol,Zadykowicz Beata,Storoniak Piotr,Wera Michał,Żamojć Krzysztof

Funder

Wroclaw Centre for Networking and Supercomputing

Polish National Science Centre

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry

Reference37 articles.

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3. Antiproliferative effect of novel aminoacridine-based compounds;Munder;Med. Chem.,2015

4. Inhibition of DNA topoisomerases I and II and growth inhibition of HL-60 cells by novel acridine-based compounds;Janočková;Eur. J. Pharmaceut. Sci.,2015

5. Theoretical studies on the prototropic tautomerism, structure, and features of acridine and 9-acridinamine free base and their protonated forms;Rak;J. Org. Chem.,1992

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1. The crystal structure of N-(acridin-9-yl)-4-chloro-N-(4-chloro-butanoyl) butanamide, C₂₁H₂₀Cl₂N₂O₂;Zeitschrift für Kristallographie - New Crystal Structures;2024-04-22

2. Synthesis and exploration of configurational dynamics in equilibrating E/Z 2-aryliminothiazolidin-4-ones using NMR and estimation of thermodynamic parameters;New Journal of Chemistry;2022