Synthesis of Polyiodides of N- and S-S-Acetonyl Derivatives of 2,2′-(Disulfanediyl)- and 2,2′-[Alkanediylbis(sulfanyl)]-bisbenzimidazolium
- Авторлар: Shagun L.G.1, Dorofeev I.A.1, Zhilitskaya L.V.1, Yarosh N.O.1, Larina L.I.1
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Мекемелер:
- Favorskii Irkutsk Institute of Chemistry, Siberian Branch
- Шығарылым: Том 55, № 8 (2019)
- Беттер: 1160-1165
- Бөлім: Article
- URL: https://bakhtiniada.ru/1070-4280/article/view/221059
- DOI: https://doi.org/10.1134/S1070428019080153
- ID: 221059
Дәйексөз келтіру
Аннотация
2,2′-(Disulfanediyl)- and 2,2′-[alkanediylbis(sulfanyl)]-bisbenzimidazoles react with aliphatic, aromatic, and heterocyclic α-iodoketones in the presence of elemental iodine without solvents, basic media, and catalysts to afford polyiodides of the N- and S-S-acetonyl derivatives. The selectivity of the alkylation reaction depends on the structure of the starting substrates. In the case of the disulfide, the reaction involves the sulfur atoms to give hitherto unknown disulfanium derivatives. The introduction of an organic bridge between the sulfur atoms leads to the formation of polyiodides of 2,2′-[alkanediylbis(sulfanyl)]bisbenzimidazole N-acetonyl derivatives.
Авторлар туралы
L. Shagun
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: lara_zhilitskaya@irioch.irk.ru
Ресей, ul. Favorskogo 1, Irkutsk, 664033
I. Dorofeev
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: lara_zhilitskaya@irioch.irk.ru
Ресей, ul. Favorskogo 1, Irkutsk, 664033
L. Zhilitskaya
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Хат алмасуға жауапты Автор.
Email: lara_zhilitskaya@irioch.irk.ru
Ресей, ul. Favorskogo 1, Irkutsk, 664033
N. Yarosh
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: lara_zhilitskaya@irioch.irk.ru
Ресей, ul. Favorskogo 1, Irkutsk, 664033
L. Larina
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: lara_zhilitskaya@irioch.irk.ru
Ресей, ul. Favorskogo 1, Irkutsk, 664033
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