1 H, 13 C and 15 N NMR of spiro acridines integrated with pyrrole scaffolds-Reference-Cited by-同舟云学术

1 H, 13 C and 15 N NMR of spiro acridines integrated with pyrrole scaffolds

Published:2019-12-09 Issue:2 Volume:58 Page:204-214
ISSN:0749-1581
Container-title:Magnetic Resonance in Chemistry
language:en
Short-container-title:Magn Reson Chem

Author:

Vilková Mária¹^ORCID,Šoral Michal²,Bečka Michal¹,Potočňák Ivan¹,Sabolová Danica¹,Béres Tibor³,Dušek Michal⁴,Imrich Ján¹

Affiliation:

1. Institute of Chemistry, Faculty of Science, P. J. Šafárik University; Košice Slovakia

2. Central Laboratories, Faculty of Chemical and Food Technology; Slovak University of Technology in Bratislava; Bratislava Slovakia

3. Centre of the Region Haná for Biotechnological and Agricultural Research, Department of the Phytochemistry, Faculty of Science; Palacký University; Olomouc Czech Republic

4. Institute of Physics, Czech Academy of Sciences; Praha Czech Republic

Funder

Grant Agency for Science of the Slovak Ministry of Education

Operation Program Prague Competitiveness

Research & Development Operational Program

Grant Agency for Science

Publisher

Wiley

Subject

General Materials Science,General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mrc.4974/fullpdf

Reference20 articles.

1. Recent developments in the synthesis and biological activity of acridine/acridone analogues

2. A review on acridinylthioureas and its derivatives: biological and cytotoxic activity

3. Acridine and its derivatives: a patent review (2009 – 2013)

4. Novel bis(indolyl)hydrazide–hydrazones as potent cytotoxic agents

5. Synthesis and anti-tumor evaluation of novel hydrazide and hydrazide-hydrazone derivatives

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