Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Serap Basoglu Ozdemir"'
Autor:
Cigdem Dokuzparmak, Fulya Oz Tuncay, Serap Basoglu Ozdemir, Busra Kurnaz, Ilke Demir, Ahmet Colak, Safiye Sag Erdem, Nuri Yildirim
In this study, a series of new organic compounds with piperazine as a fundamental skeleton was synthesized and evaluated for their tyrosinase inhibitory potentials by in vitro and in silico studies. The in vitro studies have shown that compounds 10a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7877fcbe6f4bff7355d989f59f1003ab
https://hdl.handle.net/11424/286137
https://hdl.handle.net/11424/286137
Autor:
Neslihan Demirbas, Yıldız Uygun Cebeci, Ahmet Demirbas, Şengül Alpay Karaoğlu, Serap Basoglu Ozdemir
Publikováno v:
Archive of Biomedical Science and Engineering. :010-020
Tryptamine was converted to the corresponding 1,2,4-triazole, 1,3,4-oxadiazole, 5-oxo-1,3-thia(oxa)zolidine and 5-(4-chlorophenyl)-1,3-thia(oxa)zole derivatives via several steps. 1,3,4-oxadiazole and 1,2,4-triazoles were then converted to the corres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b68e316a093e944a7668dcb50e18e92d
https://doi.org/10.17352/abse.000009
https://doi.org/10.17352/abse.000009
Publikováno v:
Journal of Heterocyclic Chemistry. 55:2744-2759
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::618ed881367bc4c90c54577ff6611f6c
https://doi.org/10.1002/jhet.3336
https://doi.org/10.1002/jhet.3336
Publikováno v:
ChemistrySelect. 3:2144-2151
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bdaaa3df5ed73ed69ef5f3bc0a1bd886
https://doi.org/10.1002/slct.201800019
https://doi.org/10.1002/slct.201800019
Autor:
Sengul Alpay-Karaoglu, Serap Basoglu Ozdemir, Yıldız Uygun Cebeci, Ahmet Demirbas, Hacer Bayrak, Neslihan Demirbas, Sule Ceylan
Publikováno v:
ChemistrySelect. 2:11402-11407
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2fb3dad27e29dbb21e8076dc5cb0fac
https://doi.org/10.1002/slct.201702097
https://doi.org/10.1002/slct.201702097
Autor:
Yıldız Uygun Cebeci, Ahmet Demirbas, Sule Ceylan, Şengül Alpay Karaoğlu, Serap Basoglu Ozdemir, Hacer Bayrak, Neslihan Demirbas
Publikováno v:
Current Organic Synthesis. 15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8eece50e9ea58b4ae485a1d79cada0e3
https://doi.org/10.2174/1570179415666180118130403
https://doi.org/10.2174/1570179415666180118130403
Autor:
Yıldız Uygun Cebeci, Ahmet Demirbas, Fatma Aksakal, Şengül Alpay Karaoğlu, Hacer Bayrak, Neslihan Demirbas, Serap Basoglu Ozdemir
WOS: 000447141100008 1,3,4-oxadiazole-2-thiole 6 was obtained from 4-(2-fluoro-4-nitrophenyl)morpholine (2) by the reduction of its nitro group and the sequential treatment of the resulting amine with ethyl bro-moacetate, hydrazine hydrate, and carbo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b21948defb318ae9c9213d5e0f3d2257
https://hdl.handle.net/11436/1927
https://hdl.handle.net/11436/1927
Autor:
Arif Mermer, Neslihan Demirbas, Ahmet Demirbas, Hacer Bayrak, Serap Basoglu Ozdemir, Sule Ceylan, Yıldız Uygun Cebeci
Publikováno v:
Letters in Drug Design & Discovery. 14
Background: The amine (2) was prepared starting from 1-(4-fluorophenyl) piperazine via two steps, and then converted to the corresponding hydrazide (4). The reaction of hydrazide (4) with carbon disulfide generated the corresponding 1,3,4-oxadiazole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c7e353ab3f46884bcfb93fe3c1327d1
https://doi.org/10.2174/1570180814666170113145023
https://doi.org/10.2174/1570180814666170113145023
Autor:
Ahmet Demirbas, Serap Basoglu Ozdemir, Neslihan Demirbas, Serpil Demirci, Faik Ahmet Ayaz, Arif Mermer, Serdar Ülker, Fatma Aksakal
WOS: 000402444600015 Azole derivatives (3, 6) obtained starting from 1-(2-methoxyphenyl)piperazine were converted to the corresponding Mannich bases containing beta-lactame or flouroquinolone core via a one pot three component reaction. The synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::592bb263a36ab2eba95cf3ee501f1d6b
https://hdl.handle.net/20.500.12697/2454
https://hdl.handle.net/20.500.12697/2454
Autor:
Serap Basoglu Ozdemir, Sule Ceylan, Yıldız Uygun Cebeci, Hacer Bayrak, Ahmet Demirbas, Şengül Alpay Karaoğlu, Neslihan Demirbas, Arif Mermer
Alpay Karaoglu, Sengul/0000-0003-1047-8350 WOS: 000394434400008 The hydrazide 5, that was obtained from -1-(4-fluorophenyl) piperazine (1), was converted to the cor-responding carbothioamides 6a-c by the reaction with alkyl(aryl) isothiocyanates. the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c60299ae06cbcf0a4ad1d1362ffd72be
https://hdl.handle.net/11494/2971
https://hdl.handle.net/11494/2971