Long-Range 1H–15N J Couplings Providing a Method for Direct Studies of the Structure and Azide–Tetrazole Equilibrium in a Series of Azido-1,2,4-triazines and Azidopyrimidines-Reference-Cited by-同舟云学术

Long-Range 1H–15N J Couplings Providing a Method for Direct Studies of the Structure and Azide–Tetrazole Equilibrium in a Series of Azido-1,2,4-triazines and Azidopyrimidines

Published:2013-06-27 Issue:14 Volume:78 Page:6975-6982
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Shestakova Tatyana S.¹,Shenkarev Zakhar O.²,Deev Sergey L.¹,Chupakhin Oleg N.¹³,Khalymbadzha Igor A.¹,Rusinov Vladimir L.¹,Arseniev Alexander S.²

Affiliation:

1. Ural Federal University, 19 Mira Street, 620002 Ekaterinburg, Russia

2. Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, 16/10 Miklukho-Maklaya Street, 117997 Moscow, Russia

3. I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, 22 S. Kovalevskoy Street, 620219 Ekaterinburg, Russia

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo4008207

Reference43 articles.

1. 2-Triazole-Substituted Adenosines: A New Class of Selective A3 Adenosine Receptor Agonists, Partial Agonists, and Antagonists

2. Inhibition of Siderophore Biosynthesis by 2-Triazole Substituted Analogues of 5′-O-[N-(Salicyl)sulfamoyl]adenosine: Antibacterial Nucleosides Effective against Mycobacterium tuberculosis

3. Azide−Tetrazole Equilibrium of C-6 Azidopurine Nucleosides and Their Ligation Reactions with Alkynes

4. “Click-chemistry” approach in the design of 1,2,3-triazolyl-pyridine ligands and their Ru(ii)-complexes for dye-sensitized solar cells

5. Clicked dipicolinic antennae for lanthanide luminescent probes

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