Ring Opening of 4-Arylamino-2-tert-butyl-5-oxo-2,5-dihydrofuran-2-yl Acetates with Aromatic and Heterocyclic Amines
- 作者: Igidov N.M.1, Rubtsov A.E.2
-
隶属关系:
- Perm State Pharmaceutical Academy
- Perm State National Research University
- 期: 卷 55, 编号 10 (2019)
- 页面: 1459-1464
- 栏目: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/221241
- DOI: https://doi.org/10.1134/S1070428019100026
- ID: 221241
如何引用文章
详细
Reactions of 4-arylamino-2-tert-butyl-5-oxo-2,5-dihydrofuran-2-yl acetates with an equimolar amount of aromatic or heterocyclic amine in toluene involves initial attack of the amine on the C2 atom of the furan ring, followed by opening of the furan ring and elimination of acetic acid to give N-aryl(hetaryl)-2-arylamino-5,5-dimethyl-4-oxohex-2-enamides.
作者简介
N. Igidov
Perm State Pharmaceutical Academy
Email: rubtsov@psu.ru
俄罗斯联邦, Perm
A. Rubtsov
Perm State National Research University
编辑信件的主要联系方式.
Email: rubtsov@psu.ru
俄罗斯联邦, Perm
补充文件
