Výsledky vyhledávání - "Svitlana I. Sabat"

Synthesis of condensed S-, N- containing heterocyclic systems on the base of 2-amino-4,9-dioxo-4,9-dihydronaphto[2,3-b]thiophene-3-ethylcarboxilate

Autor: Volodymyr Novikov, Maryna Stasevych, Svitlana I. Sabat, Rostyslav Ya. Musyanovych

Publikováno v: Chemistry & Chemical Technology. 2:157-162

Synthesis of a new 2-aryl-4Н-naphtho[2’,3’,4,5]thieno[2,3-d][1,3]oxazine-4,5,10-triones, 2-arylnaphtho[2’,3’,4,5]thieno[2,3-d][1,3]pyrimidine-4,5,10(3Н)-triones, 3-phenyl naphtho[2’,3’,4,5]thieno[2,3-d][1,3]pyrimidine-2,4,5,10(1Н, 3Н)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::433b514d593e52ffd1d17d1ad1c861e2
https://doi.org/10.23939/chcht02.03.157

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Sulfur-containing derivatives of 1,4-naphthoquinone, part 1: Disulfide synthesis

Autor: Svitlana I. Sabat, Maryna Stasevych, Mykola O. Platonov, Rostyslav Ya. Musyanovych, Volodymyr Novikov, Maxym Yu. Plotnikov

Publikováno v: Heteroatom Chemistry. 16:205-211

Disulfides of 1,4-naphthoquinone were synthesized, and different methods of their synthesis were investigated. High yields and purity of disulfides were obtained from the oxidation of thiol derivatives. The latter were prepared in high yields and pur

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f35e93fc96daa4d739488cc673270714
https://doi.org/10.1002/hc.20112

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Sulfur-containing derivatives of 1,4-naphthoquinone, part 2: Sulfenyl derivative synthesis

Autor: Rostyslav Ya. Musyanovych, Volodymyr Novikov, Svitlana I. Sabat, Mykola O. Platonov, Maryna Stasevych, Maxym Yu. Plotnikov

Publikováno v: Heteroatom Chemistry. 16:587-598

Sulfenylchlorides, sulfenates, and sulfenamides of 1,4-naphthoquinone were synthesized, and different methods of their syntheses were investigated. Synthesized sulfenates and sulfenamides are stable due to the large electron-withdrawing potential of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3f2a0cc2eac8fdff6d52c78204595aa6
https://doi.org/10.1002/hc.20157

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