Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Şule Bahçeci"'
Autor:
Haydar Yüksek, Muzaffer Alkan, Şule Bahçeci, Onur Akyıldırım, Murat Beytur, Mehmet Lütfi Yola
Publikováno v:
Pamukkale University Journal of Engineering Sciences, Vol 23, Iss 7, Pp 874-876 (2017)
Camsı karbon elektrot (GCE), 3-Methyl-4-(4-hydroxybenzylidenamino)-4,5-dihydro-1H-1,2,4-triazol-5-one (MDT)’ nin fenol oksidasyonu ile 0.1 M destek elektrolit içinde modifiye olmuştur. Modifiye edilmiş yüzey, birkaç teknik kullanılarak ile k
Externí odkaz:
https://doaj.org/article/19d93ef00218413da24fd1a02b71d863
Publikováno v:
Molbank, Vol 2006, Iss 1, p M463 (2006)
n/a
Externí odkaz:
https://doaj.org/article/1bc10fd5ac1044129acd75a0d49b8a35
Publikováno v:
Volume: 3, Issue: 1 27-32
Turkish Journal of Analytical Chemistry
Turkish Journal of Analytical Chemistry
The acidic properties of ten 3-alkyl(aryl)-4-[3-hydroxy-4-methoxy benzylidenamino]-4,5-dihydro-1H-1,2,4-triazol-5-one derivatives were investigated. In this study, isopropyl alcohol and tert‐butanol were used as an amphiprotic solvent. Aceton and N
Autor:
Muzaffer Alkan, Murat Beytur, Şule Bahçeci, Onur Akyildirim, Haydar Yüksek, Mehmet Lütfi Yola
Publikováno v:
Pamukkale University Journal of Engineering Sciences. 23:874-876
WOS: 000443172200011
Cadmium is recently threatening not only the life of man but also nature and living environment. In addition, cadmium usage is generally decreasing because it is toxic. 3-Methyl-4- (4-hydroxybenzylidenamino)-4,5-dihydro-1H-1
Cadmium is recently threatening not only the life of man but also nature and living environment. In addition, cadmium usage is generally decreasing because it is toxic. 3-Methyl-4- (4-hydroxybenzylidenamino)-4,5-dihydro-1H-1
3-Methyl-4-(3-benzoxy-4-methoxybenzylidenamino)-4,5-dihydro-1H-1,2,4-triazol-5-one molecule was optimized by using the B3LYP/HF 631G(d,p) and B3LYP/HF 6311G(d,p) basis sets. This optimized structures used to calculation of the different theoretical p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25d4bcce67b5f59f5dd6debfb34f5af5
Autor:
Zafer Ocak, Muzaffer Alkan, Haydar Yüksek, Elif Ağyel, Haci Baykara, Ozlem Aktaş, Şule Bahçeci, Ismail Cakmak
Publikováno v:
Journal of Molecular Structure. 873:142-148
3-Alkyl-4-amino-4,5-dihydro-1 H -1,2,4-triazol-5-ones ( 2 ) reacted with p -methoxybenzoyl chloride to afford the corresponding 3-alkyl-4-( p -methoxybenzoylamino)-4,5-dihydro-1 H -1,2,4-triazol-5-ones ( 3 ). Five newly synthesized compounds have bee
Autor:
Mustafa Özdemir, Mahfuz Elmastas, Mustafa Calapoğlu, Haydar Yüksek, Şule Bahçeci, Hüseyin Akşit, Muzaffer Alkan, Fatih İslamoğlu
Publikováno v:
Molecules, Vol 12, Iss 8, Pp 1805-1816 (2007)
Molecules; Volume 12; Issue 8; Pages: 1805-1816
Molecules; Volume 12; Issue 8; Pages: 1805-1816
WOS:000250488300018 PubMed: 17960089 Five novel 3-alkyl-4-phenylacetylamino-4,5-dihydro-1H-1,2,4-triazol-5-ones (2) were synthesized by the reactions of 3-alkyl-4-amino-4,5-dihydro-1H-1,2,4-triazol-5ones (1) with phenylacetyl chloride and characteriz
Publikováno v:
Molecules, Vol 10, Iss 8, Pp 961-970 (2005)
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules
Volume 10
Issue 8
Pages 961-970
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules
Volume 10
Issue 8
Pages 961-970
The synthesis of 3-alkyl(aryl)-4-(3-ethoxy-4-hydroxybenzylidenamino)-4,5-dihydro-1H-1,2,4-triazol-5-ones 3 from the reactions of 3-alkyl(aryl)-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones 2 with 3-ethoxy-4-hydroxybenzaldehyde is described. The acetyla
Publikováno v:
Molecules, Vol 9, Iss 4, Pp 232-240 (2004)
Molecules
Volume 9
Issue 4
Pages: 232-240
Molecules
Volume 9
Issue 4
Pages: 232-240
3-Alkyl(Aryl)-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones (2) reacted with 2-furoyl chloride and thiophene-2-carbonyl chloride to afford the corresponding 3- alkyl(aryl)-4-(2-furoylamino)-4,5-dihydro-1H-1,2,4-triazol-5-ones (3) and 3-alkyl(aryl)- 4-(
Publikováno v:
Collection of Czechoslovak Chemical Communications. 67:1215-1222
The synthesis of 3-alkyl(aryl)-4-[4-(dimethylamino)benzylideneamino]-4,5-dihydro-1H-1,2,4-triazol-5-ones (3) from the reactions of 3-alkyl(aryl)-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones (2) with 4-(dimethylamino)benzaldehyde is described. The newl