Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yuriy N. Markitanov"'
Publikováno v:
Chemistry of Heterocyclic Compounds. 57:1149-1154
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f7dede440e49ebdd2bcb5c8684e1fb7
https://doi.org/10.1007/s10593-021-03035-w
https://doi.org/10.1007/s10593-021-03035-w
Publikováno v:
Chemistry of Heterocyclic Compounds. 57:253-260
Cycloaddition reactions of 3,3,3-trifluoropropene derivatives containing an alkoxycarbonyl, sulfonyl, sulfoximine, or sulfamide substituent in position 1 with ethyl isocyanoacetate proceed with the formation of 3-(trifluoromethyl)-2,3-dihydro-1H-pyrr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1953f4658c439bf799091edebe4c3f67
https://doi.org/10.1007/s10593-021-02901-x
https://doi.org/10.1007/s10593-021-02901-x
Autor:
Yuriy G. Shermolovich, Timofii V. Rudenko, Eduard B. Rusanov, Yuriy N. Markitanov, Sergiy S. Mykhaylychenko
Publikováno v:
Chemistry of Heterocyclic Compounds. 55:189-192
New 4-polyfluoroalkyl-1,3-dithiolanes were synthesized by reaction of polyfluoroalkanethioamides with thiocarbonyl ylide that was generated in situ by desilylation of chloromethyl (trimethylsilyl)methyl sulfide with tetramethylammonium fluoride.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb19fdad8e32440f32616f9fe61440fe
https://doi.org/10.1007/s10593-019-02438-0
https://doi.org/10.1007/s10593-019-02438-0
1,3-Dipolar cycloaddition of 1-substituted 3,3,3-trifluoropropenes to ethyl cyanocarboxylate N-oxide
Publikováno v:
Chemistry of Heterocyclic Compounds. 54:89-92
3,3,3-Trifluoropropene derivatives containing a sulfonyl, sulfoximine, or sulfamide substituent at position 1 were used in 1,3-dipolar cycloaddition reaction with ethyl cyanocarboxylate N-oxide generated by thermal decomposition of ethyl oximinochlor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7e6b786883f3f7cb95c4763af2e31f9
https://doi.org/10.1007/s10593-018-2236-8
https://doi.org/10.1007/s10593-018-2236-8
Autor:
Yuriy N. Markitanov, Vadim M. Timoshenko, Yuriy G. Shermolovich, Vladimir L. Mykhalchuk, Andrei V. Grafov, Irina A. Grafova
Publikováno v:
Chemistry of Heterocyclic Compounds. 52:503-506
New 4-(trifluoromethyl)pyrrolidines containing sulfonyl, iminosulfonyl, sulfamide, or phosphonyl group at position 3 were synthesized by 1,3-dipolar cycloaddition reactions of 3,3,3-trifluoropropene derivatives to azomethine ylide generated in situ f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afbc361e0f7d9af022d74da3f501965b
https://doi.org/10.1007/s10593-016-1916-5
https://doi.org/10.1007/s10593-016-1916-5