Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Anton V. Zhemera"'
Autor:
Yurii S. Moroz, Anton V. Zhemera, Andrey V. Bogolyubsky, Anzhelika I. Konovets, Kateryna E. Gubina, Olena Savych, Volodymyr Brovarets, Dmytro N. Khomenko, Yuliya O. Kuchkovska, Roman Doroschuk, Sergey E. Pipko, Oleksandr O. Grygorenko, Alexander V. Grishchenko
Publikováno v:
ACS Comb Sci
Two protocols for the combinatorial synthesis of 5-(dialkylamino)tetrazoles were developed. The best success rate (67%) was shown by the method which used primary and secondary amines, 2,2,2-trifluoroethylthiocarbamate and sodium azide as the startin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a4c96f644fa6674560036cab95cd46e
https://doi.org/10.1021/acscombsci.9b00120
https://doi.org/10.1021/acscombsci.9b00120
Autor:
Anton V. Zhemera, Anzhelika I. Konovets, Alexander V. Grishchenko, Andrey V. Bogolubsky, Yurii V. Dmytriv, Roman Doroschuk, Yurii S. Moroz, Andrey A. Tolmachev, Pavel K. Mykhailiuk, Sergey E. Pipko, Olga A. Zaporozhets
Publikováno v:
European Journal of Organic Chemistry. 2016:2120-2130
A simple parallel synthesis approach to unsymmetrical N1,N2-substituted aliphatic oxamides using methyl (2,2,2-trifluoroethyl) oxalate and bis(2,2,2-trifluoroethyl) oxalate was developed. The method was validated on a 52-membered set of the oxamides,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62d0e46d71ed35754af0816617db309b
https://doi.org/10.1002/ejoc.201501579
https://doi.org/10.1002/ejoc.201501579
Autor:
Andrey V. Bogolyubsky, Volodymyr Brovarets, Roman O. Doroshchuk, Alexander V. Grishchenko, Sergey E. Pipko, Olena Savych, Dmytro N. Khomenko, Anzhelika I. Konovets, Mykhailo Vybornyi, Anton V. Zhemera, Yurii S. Moroz
Publikováno v:
ACS combinatorial science. 20(7)
A 1,2,4-triazole motif is present in numerous commercialized and investigational bioactive molecules. Despite its importance for medicinal chemistry, there is a lack of convenient combinatorial approaches toward this molecular core. Herein, we presen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d6a9a69ecf356c61da69848107459ac
https://pubmed.ncbi.nlm.nih.gov/29874036
https://pubmed.ncbi.nlm.nih.gov/29874036
Autor:
Anton V. Zhemera, Oleksandr O. Viniychuk, Andrey V. Bogolubsky, Anzhelika I. Konovets, Pavel K. Mykhailiuk, Yurii S. Moroz, Andrey A. Tolmachev, Sergey E. Pipko, Olga A. Zaporozhets, Alexander V. Grishchenko, Dmytro V. Ushakov
Publikováno v:
ACS combinatorial science. 18(10)
One-pot synthesis of 3,5-disubstituted 1,2,4-oxadiazoles from carboxylic acids and nitriles was optimized to parallel chemistry. The method was validated on a 141 member library; the desired products were recovered with a high success rate and in mod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87ee1d567c772fd8ffdbf7ac1e659c78
https://pubmed.ncbi.nlm.nih.gov/27548754
https://pubmed.ncbi.nlm.nih.gov/27548754
Autor:
Sergey E. Pipko, Yurii V. Dmytriv, Olga A. Zaporozhets, Pavel K. Mykhailiuk, Alexander V. Grishchenko, Yurii S. Moroz, Andrey V. Bogolubsky, Anton V. Zhemera, Andrey A. Tolmachev, Roman Doroschuk, Anzhelika I. Konovets
Publikováno v:
European Journal of Organic Chemistry. 2016
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fca4b8b463c386b94cea82884823e1f
https://doi.org/10.1002/ejoc.201690022
https://doi.org/10.1002/ejoc.201690022
Autor:
Anzhelika I. Konovets, Anton V. Zhemera, Yurii S. Moroz, Olena O. Stepaniuk, Andrey A. Tolmachev, Andrey V. Bogolubsky, Pavel K. Mykhailiuk, Roman Doroschuk, Yurii V. Dmytriv, Inna S. Myronchuk, Olga A. Zaporozhets, Sergey E. Pipko
Publikováno v:
ACS combinatorial science. 17(10)
A one-pot parallel synthesis of N(1)-aryl-N(2)-alkyl-substituted oxamides with 2,2,2-trifluoroethyl chlorooxoacetate was developed. The synthesis of a library of 45 oxamides revealed higher efficiency of this reagent over the known ethyl chlorooxoace
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5da22504707d75cdd6b689a221264629
https://pubmed.ncbi.nlm.nih.gov/26325360
https://pubmed.ncbi.nlm.nih.gov/26325360