Synthesis of Polyiodides of N- and S-S-Acetonyl Derivatives of 2,2′-(Disulfanediyl)- and 2,2′-[Alkanediylbis(sulfanyl)]-bisbenzimidazolium
- 作者: Shagun L.G.1, Dorofeev I.A.1, Zhilitskaya L.V.1, Yarosh N.O.1, Larina L.I.1
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隶属关系:
- Favorskii Irkutsk Institute of Chemistry, Siberian Branch
- 期: 卷 55, 编号 8 (2019)
- 页面: 1160-1165
- 栏目: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/221059
- DOI: https://doi.org/10.1134/S1070428019080153
- ID: 221059
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详细
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.
作者简介
L. Shagun
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: lara_zhilitskaya@irioch.irk.ru
俄罗斯联邦, ul. Favorskogo 1, Irkutsk, 664033
I. Dorofeev
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: lara_zhilitskaya@irioch.irk.ru
俄罗斯联邦, ul. Favorskogo 1, Irkutsk, 664033
L. Zhilitskaya
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
编辑信件的主要联系方式.
Email: lara_zhilitskaya@irioch.irk.ru
俄罗斯联邦, ul. Favorskogo 1, Irkutsk, 664033
N. Yarosh
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: lara_zhilitskaya@irioch.irk.ru
俄罗斯联邦, ul. Favorskogo 1, Irkutsk, 664033
L. Larina
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: lara_zhilitskaya@irioch.irk.ru
俄罗斯联邦, ul. Favorskogo 1, Irkutsk, 664033
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