Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Veronika Ručilová"'
Publikováno v:
Advanced Synthesis & Catalysis. 363:1112-1119
Autor:
Dominik Vítek, Marek Zatloukal, Jiří Voller, Marian Hajduch, Miroslav Strnad, Beata Monfort, Libor Havlíček, Veronika Ručilová, Alena Kadlecová, Prashant Khirsariya, Gabriel Gonzalez, Kamil Paruch, Miroslav Soural, Barbara Maková, Václav Mik, Martina Medvedíková, Barbora Lišková, Benoît D'Autréaux, Zoila Gándara Barreiro
Publikováno v:
Bioorganic and Medicinal Chemistry
Bioorganic and Medicinal Chemistry, Elsevier, 2021, 33, pp.115993. ⟨10.1016/j.bmc.2021.115993⟩
Bioorganic and Medicinal Chemistry, 2021, 33, pp.115993. ⟨10.1016/j.bmc.2021.115993⟩
Bioorganic and Medicinal Chemistry, Elsevier, 2021, 33, pp.115993. ⟨10.1016/j.bmc.2021.115993⟩
Bioorganic and Medicinal Chemistry, 2021, 33, pp.115993. ⟨10.1016/j.bmc.2021.115993⟩
Kinetin (N6-furfuryladenine), a plant growth substance of the cytokinin family, has been shown to modulate aging and various age-related conditions in animal models. Here we report the synthesis of kinetin isosteres with the purine ring replaced by o
Autor:
Petr Funk, Maciej Pawłowski, Barbara Nowak, Elżbieta Wyska, Barbora Lemrová, Artur Świerczek, Adam Bucki, Alicja Gawalska, Grażyna Chłoń-Rzepa, Paweł Zajdel, Krzysztof Pociecha, Veronika Ručilová, Monika Zadrożna, Miroslav Soural, David Vanda
Publikováno v:
European journal of medicinal chemistry. 209
Herein, we describe the rapid synthesis of a focused library of trisubstituted imidazo[4,5-b]pyridines and imidazo[4,5-c]pyridines from 2,4-dichloro-3-nitropyridine using the combination of solution-phase/solid-phase chemistry as new potential anti-i
Publikováno v:
ACS Combinatorial Science. 20:529-543
In this review, we summarize synthetic approaches to preparing single or fused oxazine and thiazine derivatives using solid-phase synthesis (SPS). The literature survey revealed that diverse compounds bearing variously functionalized 1,2-oxazine, 1,3
Autor:
Veronika Ručilová, Miroslav Soural
Publikováno v:
Synthesis. 50:3809-3824
The synthesis of pharmacologically relevant scaffolds is an important goal in modern organic chemistry. For this reason, the use of methodologies involving operationally simple procedures and easily handled reagents to chemoselectively and stereosele
Publikováno v:
European Journal of Organic Chemistry. 2018:564-570
Publikováno v:
European Journal of Organic Chemistry. 2017:7034-7039
Herein, we report a simple synthesis of disubstituted pyrazino-oxazines with controlled stereochemistry using readily available building blocks: N-Fmoc-protected α-amino acids and 2-bromoketones. The convenient solid-phase synthesis afforded polymer
Polymer-Supported Stereoselective Synthesis of Benzoxazino[4,3-b][1,2,5]thiadiazepinone 6,6-dioxides
Publikováno v:
ACS combinatorial science. 19(10)
Herein, we report the stereoselective synthesis of trisubstituted benzoxazino[4,3-b][1,2,5]thiadiazepinone 6,6-dioxides from polymer-supported Fmoc-Ser(tBu)-OH and Fmoc-Thr(tBu)-OH. After the solid-phase synthesis of N-alkylated-N-sulfonylated interm