Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Taras V. Omelian"'
Autor:
Ioann O. Popov, Oleksandr O. Grygorenko, Svitlana V. Shishkina, Taras V. Omelian, Maria V. Popova, Yulian M. Volovenko, Alexey V. Dobrydnev, Irina S. Konovalova
Publikováno v:
ChemistrySelect. 6:3084-3088
Autor:
Pavlo O. Iegorov, Taras V. Omelian, Yulian M. Volovenko, Anton O. Poliudov, Alexey V. Dobrydnev, Eugeniy N. Ostapchuk
Publikováno v:
Chemistry of Heterocyclic Compounds. 57:207-211
A number of 2-substituted 4–7-membered cyclic amino acid esters bearing endocyclic amino group were sequentially mesylated and cyclized via the CSIC reaction strategy to give the key precursors 3a-substituted bicyclic isothiazolidin-4-one 1,1-dioxi
Autor:
Taras V. Omelian, Irina S. Konovalova, Yulian M. Volovenko, Alexey V. Dobrydnev, Oleksandr Yu. Utchenko, Eugeniy N. Ostapchuk
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 151:1759-1772
The present work is devoted to the study of the reactivity of tetrahydropyrrolo[1,2-b]isothiazol-3(2H)-one 1,1-dioxide framework. This scaffold possesses two reaction centers: the EWG-activated methylene group and the carbonyl functionality, which ar
Autor:
Oleksandr O. Grygorenko, Volodymyr Brovarets, Yehor S. Malets, Eugeniy N. Ostapchuk, Taras V. Omelian, Alexey V. Dobrydnev
Publikováno v:
Chemistry of Heterocyclic Compounds. 56:213-218
A series of 2,2-disubstituted 8-azachromanones, including spirocyclic compounds, have been synthesized via Horner–Wadsworth– Emmons reaction. Dimethyl methylphosphonate was acylated with methyl 2-methoxypyridine-3-carboxylate to afford the key in
Autor:
Alexey V. Dodrydnev, Taras V. Omelian
Publikováno v:
Chemistry of Heterocyclic Compounds. 57:630-632
Diversity-oriented synthesis embodied in a strategy of pairing vinyl sulfonamide moiety with other functional groups resulted in an array of skeletally diverse 5–8-membered sultams (cyclic sulfonamides) in the fewest possible steps. In particular,
Autor:
Vitalii V. Izhyk, Anton O. Poliudov, Alexey V. Dobrydnev, Taras V. Omelian, Maria V. Popova, Yulian M. Volovenko
Publikováno v:
Tetrahedron. 124:133013
Publikováno v:
ChemistrySelect. 4:4933-4937