Synthesis of N-Tosylates of 4-Methoxy-1,2,3,4-tetrahydrocarbazole and 2-(6-Methoxy-1-cycloalken-1-yl)anilines
- 作者: Kirillova I.1, Zalimova М.1, Mulyukova R.2, Vakhitova Y.2, Khusnitdinov R.3, Gataullin R.3
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隶属关系:
- Bashkir State University
- Institute of Biochemistry and Genetics, Ufa Scientific Center
- Institute of Organic Chemistry
- 期: 卷 88, 编号 3 (2018)
- 页面: 418-424
- 栏目: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/222046
- DOI: https://doi.org/10.1134/S1070363218030076
- ID: 222046
如何引用文章
详细
The reaction of N-tosylates of 2-(1-cycloalken-1-yl)anilines and 2,3,9a,9-tetrahydro-1H-carbazole with methanol in the presence of CuBr2 proceeds with high regioselectivity leading to the corresponding tosylates of 2-(6-methoxy-1-cycloalken-1-yl)anilines and 4-methoxy-1,2,3,4-tetrahydrocarbazole. The latter as well as N-mesyl-1,2,3,4-tetrahydrocarbazole showed moderate cytotoxic activity with respect to HEK293 cell line.
作者简介
I. Kirillova
Bashkir State University
Email: gataullin@anrb.ru
俄罗斯联邦, Ufa
М. Zalimova
Bashkir State University
Email: gataullin@anrb.ru
俄罗斯联邦, Ufa
R. Mulyukova
Institute of Biochemistry and Genetics, Ufa Scientific Center
Email: gataullin@anrb.ru
俄罗斯联邦, Ufa
Yu. Vakhitova
Institute of Biochemistry and Genetics, Ufa Scientific Center
Email: gataullin@anrb.ru
俄罗斯联邦, Ufa
R. Khusnitdinov
Institute of Organic Chemistry
Email: gataullin@anrb.ru
俄罗斯联邦, pr. Oktyabrya 71, Ufa, 450054
R. Gataullin
Institute of Organic Chemistry
编辑信件的主要联系方式.
Email: gataullin@anrb.ru
俄罗斯联邦, pr. Oktyabrya 71, Ufa, 450054