Synthesis of [(4-Chloro-5H-1,2,3-dithiazol-5-ylidene)amino]azines

Koutentis, Panayiotis Andreas; Koyioni, Maria G.; Michaelidou, Sophia S.

doi:10.3390/molecules16118992

dc.contributor.author	Koutentis, Panayiotis Andreas	en
dc.contributor.author	Koyioni, Maria G.	en
dc.contributor.author	Michaelidou, Sophia S.	en
dc.creator	Koutentis, Panayiotis Andreas	en
dc.creator	Koyioni, Maria G.	en
dc.creator	Michaelidou, Sophia S.	en
dc.date.accessioned	2019-11-21T06:20:32Z
dc.date.available	2019-11-21T06:20:32Z
dc.date.issued	2011
dc.identifier.issn	1420-3049
dc.identifier.uri	http://gnosis.library.ucy.ac.cy/handle/7/55724
dc.description.abstract	The reactions of 2-, 3- and 4-aminopyridines with 4,5-dichloro-1,2,3- dithiazolium chloride (Appel salt) 4 to give N-(4-chloro-5H-1,2,3-dithiazol-5- ylidene)pyridin-Xamines 1a (X = 2), 1g (X = 3) and 1k (X = 4) were optimized with respect to base, temperature and reaction time. Based on these conditions a total of thirteen [(dithiazolylidene) amino]azines 1a-m were prepared and fully characterized. © 2011 by the authors	en
dc.description.abstract	licensee MDPI, Basel, Switzerland.	en
dc.source	Molecules	en
dc.source.uri	https://www.scopus.com/inward/record.uri?eid=2-s2.0-82255181722&doi=10.3390%2fmolecules16118992&partnerID=40&md5=0d39ff79981328ffc74d48b8544796ba
dc.subject	article	en
dc.subject	chemistry	en
dc.subject	synthesis	en
dc.subject	chemical structure	en
dc.subject	temperature	en
dc.subject	physical chemistry	en
dc.subject	Molecular Structure	en
dc.subject	Condensation	en
dc.subject	hydrazine derivative	en
dc.subject	thiazole derivative	en
dc.subject	Thiazoles	en
dc.subject	1,2,3-dithiazoles	en
dc.subject	4,5-dichloro-1,2,3-dithiazolium chloride	en
dc.subject	4,5 dichloro 1,2,3 dithiazolium chloride	en
dc.subject	Appel salt	en
dc.subject	aminopyridine derivative	en
dc.subject	Aminopyridines	en
dc.subject	Azine	en
dc.subject	heterocycle	en
dc.subject	Hydrazines	en
dc.subject	Physicochemical Processes	en
dc.title	Synthesis of [(4-Chloro-5H-1,2,3-dithiazol-5-ylidene)amino]azines	en
dc.type	info:eu-repo/semantics/article
dc.identifier.doi	10.3390/molecules16118992
dc.description.volume	16
dc.description.issue	11
dc.description.startingpage	8992
dc.description.endingpage	9002
dc.author.faculty	002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.department	Τμήμα Χημείας / Department of Chemistry
dc.type.uhtype	Article	en
dc.description.notes	<p>Cited By :10</p>	en
dc.source.abbreviation	Molecules	en
dc.contributor.orcid	Koutentis, Panayiotis Andreas [0000-0002-4652-7567]
dc.contributor.orcid	Koyioni, Maria [0000-0002-2786-7523]
dc.gnosis.orcid	0000-0002-4652-7567
dc.gnosis.orcid	0000-0002-2786-7523

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