Rearrangement of 7-Aryloxazolo[5,4-b]pyridines to Benzo[c][1,7]naphthyridine-4(3H)-ones and Thieno[3,2-c][1,7]naphthyridine-6(7H)-ones-Reference-Cited by-同舟云学术

Rearrangement of 7-Aryloxazolo[5,4-b]pyridines to Benzo[c][1,7]naphthyridine-4(3H)-ones and Thieno[3,2-c][1,7]naphthyridine-6(7H)-ones

Published:2020-07-09 Issue:15 Volume:85 Page:10072-10082
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Shatsauskas Anton L.¹,Mamonova Tatyana E.²,Stasyuk Anton J.³^ORCID,Chernenko Sergey A.¹,Slepukhin Pavel A.⁴,Kostyuchenko Anastasia S.¹²,Fisyuk Alexander S.¹^ORCID

Affiliation:

1. Laboratory of New Organic Materials, Omsk State Technical University, Mira Avenue, 11, 644050 Omsk, Russia

2. Department of Organic Chemistry, Omsk F. M. Dostoevsky State University, Mira Avenue, 55a, 644077 Omsk, Russia

3. Institut de Química Computacional and Departament de Química, Universitat de Girona, C/Maria Aurèlia Capmany 69, Girona, Catalonia 17003, Spain

4. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences (UB RAS), 22 Sofia Kovalevskaya Street, Yekaterinburg,620990, Russian Federation

Funder

Russian Science Foundation

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.0c01299

Reference69 articles.

1. Advances in the Chemistry of Naphthyridines

2. Adding a Hydrogen Bond May Not Help: Naphthyridinone vs Quinoline Inhibitors of Macrophage Migration Inhibitory Factor

3. bJorgensen, W. L. Macrophage Migration Inhibitory Factor Inhibitors, and Methods of Making and Using Same. U.S. Patent 20,190,144,424 A1, May 16, 2019.

4. Novel, Potent, and Orally Active Substance P Antagonists: Synthesis and Antagonist Activity of N-Benzylcarboxamide Derivatives of Pyrido[3,4-b]pyridine

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