Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Sergiy V. Zasukha"'
1
The reactions of N-trimethylsilyl substituted ethers of α- and β-amino acids with sulfur tetrafluoride and morpholinosulfur trifluoride
Autor: Sergiy V. Zasukha, Andrii Khairulin, Yuriy G. Shermolovich
Publikováno v: Journal of Sulfur Chemistry. 42:477-489
The reactions of N-trimethylsilyl derivatives of α- and β-amino acid esters with sulfur tetrafluoride lead to the formation of the corresponding difluorides of imidosulfurous acids F2S=N-X (X = α o...
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4f2bf120a77cd83b419236d419efa9e2
https://doi.org/10.1080/17415993.2021.1912045
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2
Sulfonimidamides and Imidosulfuric Diamides: Compounds from an Underexplored Part of Biologically Relevant Chemical Space
Autor: Yuriy G. Shermolovich, Vadim M. Timoshenko, Oleksii Gavrylenko, Serhii Zhersh, Sergiy V. Zasukha, Andrey A. Tolmachev, Oleksandr O. Grygorenko, Valentyna O. Pivnytska
Publikováno v: Chemistry – A European Journal. 25:6928-6940
Two novel solid reagents-1-sulfonimidoyl- and 1-sulfamimidoyl-3-methylimidazolium derivatives-for the synthesis of sulfonimidamides and imidosulfuric diamides, respectively, were developed. It is shown that these reagents are very effective in substi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca17532c1dcbf0fa82e8abc785725bd9
https://doi.org/10.1002/chem.201900440
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3
The first synthesis of chiral dialkylamines with α,α-difluoroethers fragments
Autor: Olexandr I. Guzyr, Sergiy V. Zasukha, Yuriy G. Shermolovich, Olga V. Novak
Publikováno v: Journal of Fluorine Chemistry. 185:197-200
The reaction of N -trimethylsilyl derivatives of α-aminoacids esters with sulfur tetrafluoride provides convenient synthetic route to chiral dialkylamines possessing difluoroether fragments.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2584902d1f3db0c0ae6cdb96851175c1
https://doi.org/10.1016/j.jfluchem.2016.03.010
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4
Nucleophilic Fluorination of α-Aroylphosphinates with Morpholinosulfur Trifluoride
Autor: Yuriy G. Shermolovich, Olexandr I. Guzyr, Sergiy V. Zasukha
Publikováno v: Heteroatom Chemistry. 25:256-264
Nucleophilic fluorination of aroyl-phenyl-phosphinates is highly dependent on the nature of the alkoxy substituents attached to the phosphoryl group. A reaction of aroyl-phenyl-phosphinates with morpholinosulfur trifluoride was shown to be a convenie
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3f36e2bfb81411ae64d3b2cb562e1029
https://doi.org/10.1002/hc.21171
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7
Simple Route to Adducts of (Amino)(aryl)carbene with Phosphorus Pentafluoride
Autor: Alexander B. Rozhenko, Yuriy G. Shermolovich, Alexander N. Chernega, Yurii Vlasenko, Sergiy V. Zasukha, Olexandr I. Guzyr
Publikováno v: European Journal of Inorganic Chemistry. 2013:4154-4158
The tetramethyl ester of (hydroxy)(phenyl)methylenebis(phosphonic acid) reacts with morpholinosulfur trifluoride (MOST) to provide, along with the expected product of the substitution of a hydroxy group by fluorine, the adduct of (morpholino)(phenyl)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8be22b689a5d6cce38c576ec44ccdf09
https://doi.org/10.1002/ejic.201300563
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8
ChemInform Abstract: The First Synthesis of Chiral Dialkylamines with α,α-Difluoroethers Fragments
Autor: Yuriy G. Shermolovich, Sergiy V. Zasukha, Olga V. Novak, Olexandr I. Guzyr
Publikováno v: ChemInform. 47
The reaction of N -trimethylsilyl derivatives of α-aminoacids esters with sulfur tetrafluoride provides convenient synthetic route to chiral dialkylamines possessing difluoroether fragments.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d73558d6d01eb6d0acb38d32eced73da
https://doi.org/10.1002/chin.201636052
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9
ChemInform Abstract: Nucleophilic Fluorination of α-Aroylphosphinates with Morpholinosulfur Trifluoride
Autor: Olexandr I. Guzyr, Yuriy G. Shermolovich, Sergiy V. Zasukha
Publikováno v: ChemInform. 46
Nucleophilic fluorination of aroylphosphinates is highly dependent on the nature of the alkoxy substituents attached to the phosphoryl group.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::96702a8e69b27db49e421dbc42299730
https://doi.org/10.1002/chin.201501195
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