Zobrazeno 1 - 10
of 92
pro vyhledávání: '"1 3 4-thiadiazole"'
Publikováno v:
Chimica Techno Acta, Vol 9, Iss 2 (2022)
Corrosion damages all materials, necessitating replacement and inspection related expenses. Thus, the demand has increased for new corrosion inhibitor materials. The ratios of corrosion inhibition of materials are different, but organic compounds hav
Externí odkaz:
https://doaj.org/article/ca9b0f6267bd4103b09b315b0d714ff5
Autor:
Faruk Alam
Publikováno v:
Journal of Applied Pharmaceutical Research, Vol 6, Iss 4, Pp 10-19 (2018)
A few five members’ aromatic systems having three hetero-atoms at symmetrical positions, for example, thiadiazoles have been considered broadly attributable to their intriguing pharmacological properties. These thiadiazole derivatives are the heter
Externí odkaz:
https://doaj.org/article/e3c850041bb54ef88520c97ba1663d3a
Publikováno v:
Al-Mustansiriyah Journal of Pharmaceutical Sciences, Vol 20, Iss 1 (2020)
Reaction of aqueous solution of amino acid Histidine with ethanolic solution Cinnamaldehyde to synthesize the desired Schiff base. Then, the derivative of 1, 3, 4-thiadiazole ring have been synthesized by reaction of the imine derivative with Thiosem
Externí odkaz:
https://doaj.org/article/1bae01c049d249a3ba70b73c4536bebc
Autor:
Husam A. Ameen, Ahlam J. Qasir
Publikováno v:
Iraqi Journal of Pharmaceutical Sciences, Vol 21, Iss 1 (2017)
Nitrogen heterocycles are of a special interest because they constitute an important class of natural and non natural products, many of which exhibit useful biological activities.Among these nitrogen heterocycles are 1, 3, 4-thiadiazole containing co
Externí odkaz:
https://doaj.org/article/1fe9e9b10a69484ea18b34c13e9c962d
Publikováno v:
Research in Pharmaceutical Sciences, Vol 16, Iss 6, Pp 634-642 (2021)
Research in Pharmaceutical Sciences
Research in Pharmaceutical Sciences
Background and purpose: In the last few decades, nitrogen-rich heterocyclic compounds such as 1, 3, 4-thiadiazoles, 1, 2, 4-triazoles and 1, 3, 4-oxadiazoles have received considerable attention because of their notable biological properties, especia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e97574cea0b72e5940cbf9466a026dfc
http://www.rpsjournal.net/article.asp?issn=1735-5362
http://www.rpsjournal.net/article.asp?issn=1735-5362
Autor:
Baghdad Science Journal
Publikováno v:
Baghdad Science Journal, Vol 13, Iss 2 (2016)
In this research, a new 1, 3, 4-Thiadiazole derivatives have been synthesized by many heterocyclic reactions. Starting from (2, 5 – dimercapto -1, 3, 4-Thiadiazole) a variety of derivatives have been synthesis. Compound (1) was synthesized by the r
Externí odkaz:
https://doaj.org/article/fff3aece0d0e4f52a64069b8c55e74d1
Akademický článek
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Autor:
Baghdad Science Journal
Publikováno v:
Baghdad Science Journal, Vol 5, Iss 4 (2008)
In this research, Schiff bases derived from the reaction of anthrone with different heterocyclic amines have been described. The resulted Schiff base compounds were reacted with various nucleophiles in order to obtain new heterocyclic derivatives. Ch
Externí odkaz:
https://doaj.org/article/7cc511a21ef541c29c4958023593db7d
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Anchao Chen, Zhiyun Du, Minggao Deng, Bernard Meunier, Chang-Zhi Dong, Wanzheng Zhang, Yongliang Li, Longjia Yan, Huixiong Chen
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, 2019, 60 (20), pp.1359-1362. ⟨10.1016/j.tetlet.2019.04.022⟩
Tetrahedron Letters, Elsevier, 2019, 60 (20), pp.1359-1362. ⟨10.1016/j.tetlet.2019.04.022⟩
Tetrahedron Letters, 2019, 60 (20), pp.1359-1362. ⟨10.1016/j.tetlet.2019.04.022⟩
Tetrahedron Letters, Elsevier, 2019, 60 (20), pp.1359-1362. ⟨10.1016/j.tetlet.2019.04.022⟩
International audience; An efficient and practical procedure was developed to prepare various N-pyrimidin[1,3,4]oxadiazole and thiadiazole scaffolds using a Buchwald-type coupling. The products of this reaction are otherwise difficult to access and c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6dc4dfb02ea268757d158807eee9054
https://hal.science/hal-02338726
https://hal.science/hal-02338726
