(Difluoroamino)furazans

IF 1.7 4区化学 Q3 CHEMISTRY, MULTIDISCIPLINARY

Russian Chemical Bulletin Pub Date : 2023-12-29 DOI:10.1007/s11172-023-4076-7

B. I. Ugrak, T. K. Shkineva, A. B. Sheremetev, I. L. Dalinger

引用次数: 0

Abstract

3-Amino-4-R-furazans can be converted into the corresponding 3-difluoroamino-4-R-furazans by fluorination with a fluorine—argon mixture under both liquid-phase and solid-phase conditions. Fluorinations can be enabled in the presence of both electron-donating and electron-withdrawing substituents R; some substituents R underwent transformations under fluorination conditions.

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(二氟氨基呋喃

在液相和固相条件下，3-氨基-4-R-呋喃可以通过氟氩混合物的氟化作用转化为相应的 3-二氟氨基-4-R-呋喃。氟化作用可以在有电子捐赠和电子吸收取代基 R 的情况下进行；一些取代基 R 在氟化条件下发生了转化。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Russian Chemical Bulletin 化学-化学综合

CiteScore

2.70

自引率

47.10%

发文量

257

审稿时长

3-8 weeks

期刊介绍： Publishing nearly 500 original articles a year, by leading Scientists from Russia and throughout the world, Russian Chemical Bulletin is a prominent international journal. The coverage of the journal spans practically all areas of fundamental chemical research and is presented in five sections: General and Inorganic Chemistry; Physical Chemistry; Organic Chemistry; Organometallic Chemistry; Chemistry of Natural Compounds and Bioorganic Chemistry.