| Conţinutul numărului revistei |
| Articolul precedent |
| Articolul urmator |
 |
 936 6 |
| Ultima descărcare din IBN: 2023-10-19 14:27 |
| Căutarea după subiecte similare conform CZU |
| [547+544+579.61]:615.12 (1) |
| Chimie organică (484) |
| Chimie fizică (496) |
| Microbiologie aplicată (368) |
| Farmacia în general şi profesia de farmacist (184) |
 SM ISO690:2012POPUSHOI, Ana, GULYA, Aurelian, BARBA, Nicanor, ROY, Jenny, POIRIER, Donald. Substituted 1,3-phenyl(pyridyl) propenones and derivatives with thiosemicarbazidic groups. Structrure – (hl-60) antileukemia activity relationship. In: Chemistry Journal of Moldova, 2014, nr. 2(9), pp. 67-73. ISSN 1857-1727. DOI: https://doi.org/10.19261/cjm.2014.09(2).10 |
| EXPORT metadate: Google Scholar Crossref CERIF DataCite Dublin Core |
| Chemistry Journal of Moldova | ||||||
| Numărul 2(9) / 2014 / ISSN 1857-1727 /ISSNe 2345-1688 | ||||||
|
||||||
| DOI:https://doi.org/10.19261/cjm.2014.09(2).10 | ||||||
| CZU: [547+544+579.61]:615.12 | ||||||
| Pag. 67-73 | ||||||
|
||||||
 Descarcă PDF |
||||||
| Rezumat | ||||||
3-(4-(Dimethylamino)phenyl-1-(4-isothiocyanatophenyl)prop-2-en-1-one was obtained from the corresponding N,N-dimethylthyoureas by elimination of dimethylamine at heating with gaseous hydrogen chloride in chloroform and 1-(4-isothiocyanatophenyl)-3-(pyridin-2-il)prop-2-en-1-one by treating 1,1-dimethyl-3-(4-(3-(pyridin-2-il)-acryloyl)-phenyl)thyourea with acetic anhydride. For all obtained compounds in the course of reaction the antileukemia activity was investigated |
||||||
| Cuvinte-cheie chalcones, isothiocyanatopropenones, thioureas, antileukemia activity |
||||||
|
Dublin Core Export
<?xml version='1.0' encoding='utf-8'?> <oai_dc:dc xmlns:dc='http://purl.org/dc/elements/1.1/' xmlns:oai_dc='http://www.openarchives.org/OAI/2.0/oai_dc/' xmlns:xsi='http://www.w3.org/2001/XMLSchema-instance' xsi:schemaLocation='http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd'> <dc:creator>Popuşoi, A.</dc:creator> <dc:creator>Gulea, A.P.</dc:creator> <dc:creator>Barbă, N.</dc:creator> <dc:creator>Roy, J.</dc:creator> <dc:creator>Poirier, D.</dc:creator> <dc:date>2014-01-01</dc:date> <dc:description xml:lang='en'>3-(4-(Dimethylamino)phenyl-1-(4-isothiocyanatophenyl)prop-2-en-1-one was obtained from the corresponding N,N-dimethylthyoureas by elimination of dimethylamine at heating with gaseous hydrogen chloride in chloroform and 1-(4-isothiocyanatophenyl)-3-(pyridin-2-il)prop-2-en-1-one by treating 1,1-dimethyl-3-(4-(3-(pyridin-2-il)-acryloyl)-phenyl)thyourea with acetic anhydride. For all obtained compounds in the course of reaction the antileukemia activity was investigated</dc:description> <dc:identifier>10.19261/cjm.2014.09(2).10</dc:identifier> <dc:source>Chemistry Journal of Moldova 9 (2) 67-73</dc:source> <dc:subject>chalcones</dc:subject> <dc:subject>isothiocyanatopropenones</dc:subject> <dc:subject>thioureas</dc:subject> <dc:subject>antileukemia activity</dc:subject> <dc:title>Substituted 1,3-phenyl(pyridyl) propenones and derivatives with thiosemicarbazidic groups. Structrure – (hl-60) antileukemia activity relationship</dc:title> <dc:type>info:eu-repo/semantics/article</dc:type> </oai_dc:dc>
|
|
|
