Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Ahmet Cansız"'
Autor:
Ahmet Cansız, Mehmet Barış Tabakcıoğlu
Publikováno v:
Uludağ University Journal of The Faculty of Engineering, Vol 19, Iss 1, Pp 37-46 (2014)
Dijital yayın sistemlerinde daha güvenilir yayın yapmak için kapsama alanı ve alıcı üzerindeki alan şiddetinin kestiriminde yayılım modelleri kullanılmaktadır. Yayılım modelleri temelde nümerik ve ışın izleme tekniğine dayanan mod
Externí odkaz:
https://doaj.org/article/205551f6b59c40c6a439bff756f5400e
Autor:
Alper Kus, Mustafa Karatepe, Cahit Orek, Ahmet Çetin, Ahmet Cansız, Pelin Koparir, Kamiran Sarac
Publikováno v:
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 97:606-615
The molecular geometry, vibrational frequencies, and gauge including atomic orbital (GIAO) 1 H and 13 C NMR chemical shift values of the title compound in the ground state have been calculated using the Hartree–Fock (HF) and density functional theo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acf9bb8cb8203fd15090351bff7f38eb
https://doi.org/10.1016/j.saa.2012.07.016
https://doi.org/10.1016/j.saa.2012.07.016
Publikováno v:
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 91:136-145
The title molecule, 4-allyl-5-pyridin-4-yl-2,4-dihydro-3H-1,2,4-triazole-3-thione (C10H10N4S), was synthesized and characterized by IR-NMR spectroscopy and single-crystal X-ray diffraction. The compound crystallizes in the monoclinic space group is P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88e26ee72b7d5338442ba2c686bc62d6
https://doi.org/10.1016/j.saa.2012.01.027
https://doi.org/10.1016/j.saa.2012.01.027
Publikováno v:
Transition Metal Chemistry. 32:224-227
(1R,2R)-1,2-bis-(5-amino-1,3,4-thiadiazole-2-yl)ethane-1,2-diol (L) has been prepared by the reaction of thiosemicarbazide with (2R,3R)-(+)-tartaric acid (I) and phosphorous oxychloride, and its complexes with Co(II), Ni(II) and Cu(II) have been obta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b5e58f390344a8b81a9914ac7d9bb62
https://doi.org/10.1007/s11243-006-0159-1
https://doi.org/10.1007/s11243-006-0159-1
Publikováno v:
Chemistry of Heterocyclic Compounds. 42:377-382
The synthesis of 1-aryl-3-(2-chloro-1-hydroxyethyl)-1-methylcyclobutanes, 1-aryl-3-(2-chloro-1-oxoethyl)-1-methylcyclobutanes, 2-amino-4-(3-aryl-3-methylcyclobutyl)thiazoles, and N-[4-(3-aryl-3-methylcyclobutyl)thiazole-2-yl]-N′-arylthioureas is re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a97363921fdb2ab5cd2d052cbd17420d
https://doi.org/10.1007/s10593-006-0095-1
https://doi.org/10.1007/s10593-006-0095-1
Publikováno v:
Heteroatom Chemistry. 16:503-506
A base-catalyzed condensation of diacetamido sulfides [(RNHCOCH2)2S)] with glyoxal affording thiophene-2,5-dicarboxylic acid bis-aryl(alkyl)amides has been accomplished under mild conditions. Excellent results were readily obtained when R was a subst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de842c10327b8f4f350d1f3dff46548a
https://doi.org/10.1002/hc.20153
https://doi.org/10.1002/hc.20153
Publikováno v:
Russian Journal of Organic Chemistry. 40:1813-1818
2-Amino-4-[3-methyl-3-(5,6,7,8-tetrahydro-2-naphthyl)cyclobutyl]thiazole was synthesized by reaction of 1-methyl-1-(5,6,7,8-tetrahydro-2-naphthyl)-3-chloroacetylcyclobutane with thiourea in ethanol, and its subsequent transformations afforded new der
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ac4137bea154011e729972b8d3e229a
https://doi.org/10.1007/s11178-005-0105-2
https://doi.org/10.1007/s11178-005-0105-2
Publikováno v:
Molecules; Volume 9; Issue 4; Pages: 204-212
Molecules, Vol 9, Iss 4, Pp 204-212 (2004)
Molecules, Vol 9, Iss 4, Pp 204-212 (2004)
In this study appropriate hydrazide compounds, furan-2-carboxylic acid hydrazide (1) and phenylacetic acid hydrazide (2) were converted into 1,4-substituted thiosemicarbazides 4a-e and 5a-e and 4-amino-5-(furan-2-yl or benzyl)-4H-1,2,4-triazole-3-thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64b3d1ad943cef55ef9fd9ff0d7b5289
https://doi.org/10.3390/90400204
https://doi.org/10.3390/90400204
Publikováno v:
Heteroatom Chemistry. 15:26-31
A general and convenient route for the synthesis of 2,5-di[1-methyl-1-arylcyclobutane-3-yl]- thiophenes 4a–c and bis[1-methyl-1-arylcyclobutane-3-yl]-2-(2-oxyethtylamido)thiazole sulfides 7a–c is reported. The characterization of these compounds
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::457f7a16ff60346b3ba8ec49c3c99738
https://doi.org/10.1002/hc.10207
https://doi.org/10.1002/hc.10207
Publikováno v:
Russian Journal of Organic Chemistry. 37:1542-1548
Substituted 1,5-hexadien-3-ols were synthesized by the [2,3]-Wittig rearrangement of unsymmetrical bis-allyl ethers, as well as by reactions of 1-(2-alkenyl)-2-chloromethyloxiranes with Mg/THF. The products were oxidized with pyridinium chlorochromat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::077923ee34a3fa49e7164f243b8f3f0d
https://doi.org/10.1023/a:1013843700623
https://doi.org/10.1023/a:1013843700623