Synthesis of new chiral arylsulfonamides based on carane amino alcohols

被引:0
|
作者
Grebyonkina, O. N. [1 ]
Banina, O. A. [1 ]
Rumyantsev, R. V. [2 ]
Baidamshina, D. R. [3 ]
Kolesnikova, A. I. [3 ]
Lezina, O. M. [1 ]
Rubtsova, S. A. [1 ]
机构
[1] Russian Acad Sci, Inst Chem, Ural Branch, Fed Res Ctr,Komi Sci Ctr, 48 Ul Pervomayskaya, Syktyvkar 167000, Russia
[2] Russian Acad Sci, GA Razuvaev Inst Organometall Chem, 49 Ul Tropinina, Nizhnii Novgorod 603950, Russia
[3] Kazan Fed Univ, Inst Fundamental Med & Biol, 18 Ul Kremlevskaya, Kazan 420008, Russia
关键词
monoterpenoids; (+)-3-carene; streptocide; sulfonamide; X-ray diffraction analysis; antimicrobial activity; ANTITUMOR-ACTIVITY; OLEANOLIC ACID;
D O I
10.1007/s11172-024-4345-0
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 (-)-4 beta-amino-3 alpha-hydroxy-cis-carane, was studied by X-ray diffraction. The synthesized sulfonamides and the starting amino alcohols were evaluated for antimicrobial activity.
引用
收藏
页码:2238 / 2247
页数:10
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