Synthesis of Polyiodides of N- and S-S-Acetonyl Derivatives of 2,2′-(Disulfanediyl)- and 2,2′-[Alkanediylbis(sulfanyl)]-bisbenzimidazolium


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

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

补充文件

附件文件
动作
1. JATS XML

版权所有 © Pleiades Publishing, Ltd., 2019