Synthesis of new chiral arylsulfonamides based on carane amino alcohols

IF 1.7 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
O. N. Grebyonkina, O. A. Banina, R. V. Rumyantsev, D. R. Baidamshina, A. I. Kolesnikova, O. M. Lezina, S. A. Rubtsova
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引用次数: 0

Abstract

New optically active arylsulfonamides, including carane-containing streptocide analogs, were synthesized by the reaction of carane amino alcohols with tosyl- and N-acetylsulfanilyl chlorides. Sulfonamide, which was prepared based on (–)-4β-amino-3α-hydroxy-cis-carane, was studied by X-ray diffraction. The synthesized sulfonamides and the starting amino alcohols were evaluated for antimicrobial activity.

基于甲烷氨基醇的新型手性芳基磺酰胺的合成
通过卡烷氨基醇与对甲苯磺酰氯和 N-乙酰基磺酰氯的反应,合成了新的光学活性芳基磺酰胺,包括含卡烷的链烷类似物。通过 X 射线衍射研究了以 (-)-4β- 氨基-3α-羟基顺式卡烷为基础制备的磺酰胺。对合成的磺酰胺和起始氨基醇进行了抗菌活性评估。
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来源期刊
Russian Chemical Bulletin
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.
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