NMR and DFT investigations of the substituent and solvent effect on amino-imino tautomerism in acridin-9-amines substituted at the exocyclic nitrogen atom-Reference-Cited by-同舟云学术

NMR and DFT investigations of the substituent and solvent effect on amino-imino tautomerism in acridin-9-amines substituted at the exocyclic nitrogen atom

Published:2005-06-06 Issue:8 Volume:18 Page:870-879
ISSN:0894-3230
Container-title:Journal of Physical Organic Chemistry
language:en
Short-container-title:J. Phys. Org. Chem.

Author:

Ebead Youssif,Wróblewska Agnieszka,Krzymiński Karol,Rak Janusz,Błażejowski Jerzy

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference62 articles.

1. Intersystem crossing and internal conversion quantum yields of acridine in polar and nonpolar solvents

2. Theoretical studies of drug-dinucleotide interactions. Empirical energy function calculations on the interaction of ethidium, 9-aminoacridine, and proflavin cations with the base-paired dinucleotides GpC and CpG

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