Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Ramazan, Altundas"'
Publikováno v:
ACS Omega, Vol 9, Iss 48, Pp 47884-47892 (2024)
Externí odkaz:
https://doaj.org/article/27f233ae4f78431aac2137dfa8294483
Publikováno v:
ACS Omega, Vol 9, Iss 10, Pp 11494-11499 (2024)
Externí odkaz:
https://doaj.org/article/f119e63a26264c588d3f8b7827fea0b1
Publikováno v:
Organic Communications. 13:202-206
The synthesis of precursors of neurotoxic ɣ-glutamyl β-cyanoalanine was developed starting from L-Serine via through the preparation of b-cyanoalanine and glutamyl units. Coupling of these two intermediates gave methyl ester of ɣ-glutamyl β-cyano
Publikováno v:
SSRN Electronic Journal.
Publikováno v:
Journal of CO2 Utilization. 67:102304
Publikováno v:
Microporous and Mesoporous Materials. 330:111567
One of the most important parameters to design porous polymeric materials for gas storage and separation is to discover appropriate linker. Determining the effect of linker, in fixed core, over the selectivity and adsorption has been great challenge.
Publikováno v:
Tetrahedron: Asymmetry. 28:1163-1168
The ring-opening reaction of homoserine lactone with phenylmagnesium bromides was systematically examined. A reliable method to achieve β-amino acid precursors was developed by tuning the reaction conditions to favor mono-addition to the carbonyl mo
Autor:
Hatice Seçinti, Erkan Mozioğlu, Serdar Burmaoglu, Hasan Seçen, Ahmet C. Gören, Ramazan Altundas
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 32, Iss 1, Pp 878-884 (2017)
Journal of Enzyme Inhibition and Medicinal Chemistry
Journal of Enzyme Inhibition and Medicinal Chemistry
Four multicaulin and miltirone-like phenanthrene derivatives were synthesised and evaluated as antituberculosis agents. The crucial step of the synthesis was Pschorr coupling of 4-(3-isopropyl-4-methoxyphenyl)-2-(2-aminophenyl)ethane (13) to give 2-i
Synthesis of (2S)-3-(2,4,5-trifluorophenyl)propane-1,2-diol by the Sharpless asymmetric epoxidation reaction has been achieved. 2,4,5-Trifluorobenzaldehyde with methyl 2-(triphenyl-λ5-phosphanylidene)acetate gave methyl (E)-3-(2,4,5-trifluorophenyl)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76eef70df08036855b3c547f0e4742af
Autor:
Ferhunde Aysin, Oztekin Algul, Serdar Burmaoglu, Ramazan Altundas, Busra Ozturk Aydin, Gozde Yalcin Ozkat, Ceylan Hepokur, Busra Nur Aydin, Arzu Gobek, Emine Yurtoglu, Nihal Simsek Ozek
Publikováno v:
Bioorganic Chemistry. 111:104882
Building on our previous work that discovered chalcone as a promising pharmacophore for anticancer activity, we have various other chalcone derivatives and have synthesized a series of novel bischalcone to explore their anticancer activity. Among all