Synthesis of N-Bridged 6,8-Dinitrotriazolo[1,5-a]pyridines-Reference-Cited by-同舟云学术

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Synthesis of N-Bridged 6,8-Dinitrotriazolo[1,5-a]pyridines

Published:2019-01-30 Issue:4 Volume:4 Page:1510-1515
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Starosotnikov Alexey M.¹^ORCID,Bastrakov Maxim A.¹,Knyazev Daniil A.²,Fedyanin Ivan V.³,Kachala Vadim V.¹,Dalinger Igor L.¹

Affiliation:

1. N.D. Zelinsky Institute of Organic Chemistry RAS, Leninsky prosp. 47; Moscow 119991 Russia

2. Higher Chemical College; D. Mendeleev University of Chemical Technology of Russia, Miusskaya sq. 9; Moscow 125047 Russia

3. A.N. Nesmeyanov Institute of Organoelement Compounds RAS; Vavilova str. 28 Moscow 119991 Russia

Funder

Presidium of Russian Academy of Sciences

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/slct.201803068/fullpdf

Reference61 articles.

1. Nitrogen-containing Heterocyclic Compounds 1981

2. Verfahren zur Herstellung von 1.2.4-Triazolo[1.5-a]pyridin-8-Carbonitrilen 1990

3. Comparison of inhibitory activity of isomeric triazolopyridine derivatives towards adenosine receptor subtypes or do similar structures reveal similar bioactivities?

4. Substituted Phenyltriazolopyrimidine Herbicides

5. Keeping it small, polar, and non-flat: diversely functionalized building blocks containing the privileged 5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]- and [1,5-a]pyridine cores

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1. Dinitropyridines: Synthesis and Reactions;Asian Journal of Organic Chemistry;2024-09-12

2. Nitro-substituted 2-aryl-[1,2,4]triazolo[1,5-a]azines in the reactions with C-nucleophiles;Russian Chemical Bulletin;2024-05

3. Microwave-Mediated, Catalyst-Free Synthesis of 1,2,4-Triazolo[1,5-a]pyridines from Enaminonitriles;Molecules;2024-02-18

4. Reactions of highly electrophilic azolo[b]pyridines with polyphenols;Russian Chemical Bulletin;2023-05

5. Reactions of highly electrophilic 6,8-dinitro[1,2,4]triazolo[1,5-a]pyridines with C-nucleophiles;Russian Chemical Bulletin;2023-04

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