Nucleophilic substitution reactions of 1,4-naphthoquinone and biologic properties of novel S-, S,S-, N-, and N,S-substituted 1,4-naphthoquinone derivatives-Reference-Cited by-同舟云学术

Nucleophilic substitution reactions of 1,4-naphthoquinone and biologic properties of novel S-, S,S-, N-, and N,S-substituted 1,4-naphthoquinone derivatives

Published:2013-10-10 Issue:4 Volume:23 Page:2140-2149
ISSN:1054-2523
Container-title:Medicinal Chemistry Research
language:en
Short-container-title:Med Chem Res

Author:

Ibis Cemil,Tuyun Amac Fatih,Bahar Hakan,Ayla Sibel Sahinler,Stasevych Maryna V.,Musyanovych Rostyslav Ya.,Komarovska-Porokhnyavets Olena,Novikov Volodymyr

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics

Link

http://link.springer.com/content/pdf/10.1007/s00044-013-0806-y.pdf

Reference21 articles.

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2. Guin PS, Das S, Mandal PC (2011) Electrochemical reduction of quinones in different media: a review. Int J of Electrochem 2011:1–22. doi: 10.4061/2011/816202

3. Huang LJ, Chang FC, Lee KH, Wang JP, Teng CM, Kuo SC (1998) Synthesis and antiplatelet, antiinflammatory, and antiallergic activities of substituted 3-chloro-5,8-dimethoxy-1,4-naphthoquinone and related compounds. Bioorg Med Chem 6:2261–2269

4. Huang P, Feng L, Olgham EA, Keating MJ, Plunkess W (2000) Superoxide dismutase as a target for the selective killing of cancer cells. Nature 407:390–395

5. Ibis C, Sahinler Ayla S (2011) Synthesis and spectroscopic evaluation of novel N-, S-, and O-substituted 1,4-naphthoquinone derivatives. Phosphorur Sulfur Silicon 186:2350–2356

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