Heterocyclic Analogs of 5,12-Naphthacenequinone 14*. Synthesis of naphtho[2,3-f]indole-3-carboxylic Acid Derivatives-Reference-Cited by-同舟云学术

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Heterocyclic Analogs of 5,12-Naphthacenequinone 14*. Synthesis of naphtho[2,3-f]indole-3-carboxylic Acid Derivatives

Published:2017-10 Issue:10 Volume:53 Page:1072-1079
ISSN:0009-3122
Container-title:Chemistry of Heterocyclic Compounds
language:en
Short-container-title:Chem Heterocycl Comp

Author:

Tikhomirov Alexander S.,Litvinova Valeriya A.,Luzikov Yury N.,Korolev Alexander M.,Sinkevich Yuri B.,Shchekotikhin Andrey E.

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry

Link

http://link.springer.com/article/10.1007/s10593-017-2173-y/fulltext.html

Reference28 articles.

1. Tikhomirov, A. S.; Bykov, E. E.; Luzikov Y. N.; Korolev, A. M.; Shchekotikhin, A. E. Chem. Heterocycl. Compd. 2016, 52, 797. [Khim. Geterotsikl. Soedin. 2016, 52, 797.]

2. Tikhomirov, A. S.; Shchekotikhin, A. E.; Lee, Y.-H.; Chen, Y.-A.; Yeh, C.-A. Tatarskiy, V. V.; Dezhenkova, L. G.; Glazunova, V. A.; Balzarini, J.; Shtil, A. A.; Preobrazhenskaya, M. N.; Chueh, P. J. J. Med. Chem. 2015, 58, 9522.

3. Lee, Y. R.; Chen, T. C.; Lee, C. C.; Chen, C.-L.; Ali, A. A.; Tikhomirov, A. S.; Guh, J.-H.; Yu, D.-S.; Huang, H.-S. Eur. J. Med. Chem. 2015, 102, 661.

4. Chen, W. L.; Wang, Z. H.; Feng, T. T.; Li, D. D.; Wang, C. H.; Xu, X. L.; Zhang, X. J.; You, Q. D.; Guo, X. K. Bioorg. Med. Chem. 2016, 24, 6102.

5. Mani, T.; Wang, F.; Knabe, W. E.; Sinn, A. L.; Khanna, M.; Jo, I.; Sandusky, G. E.; Sledge, G. W.; Jones, D. R.; Khanna, R.; Pollok, K.; Meroueh, S. O. Bioorg. Med. Chem. 2013, 21, 2145.

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4. СИНТЕЗ АЗОТСОДЕРЖАЩИХ ГЕТЕРОЦИКЛИЧЕСКИХ СОЕДИНЕНИЙ НА ОСНОВЕ ПРОИЗВОДНЫХ 9,10-АНТРАХИНОНА;Journal of Chemistry and Technologies;2020-10-13

5. A facile access to 2-substituted naphtho[2,3-g]quinoline-3-carboxylic acid esters via intramolecular cyclization and PyBOP-promoted functionalization;Tetrahedron;2020-09

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