Synthesis of N-nitro-N′-(trimethylsilyl)carbodiimide
- 作者: Churakov A.M.1, Ioffe S.L.1, Voronin A.A.1, Tartakovsky V.A.1
-
隶属关系:
- N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
- 期: 卷 66, 编号 6 (2017)
- 页面: 991-994
- 栏目: Full Articles
- URL: https://ogarev-online.ru/1066-5285/article/view/240691
- DOI: https://doi.org/10.1007/s11172-017-1844-2
- ID: 240691
如何引用文章
详细
Nitration of N,N′-bis(trimethylsilyl)carbodiimide with N2O5 or (NO2)2SiF6 afforded N-nitro-N´-(trimethylsilyl)carbodiimide, the first representative of N-nitro carbodiimides. Its further nitration led to the release of CO2, which is presumably formed in the course of N,N´-dinitrocarbodiimide decomposition. The reactions of N-nitro-N´-(trimethylsilyl)carbodiimide with nucleophiles take place both at the tri methylsilyl group (for example, with NH3) to give nitrocyanamide salts and at the carbodiimide C atom (for example, with Et2NH) to give the corresponding nitroguan idines.
作者简介
A. Churakov
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
编辑信件的主要联系方式.
Email: churakov@ioc.ac.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991
S. Ioffe
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: churakov@ioc.ac.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991
A. Voronin
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: churakov@ioc.ac.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991
V. Tartakovsky
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: churakov@ioc.ac.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991
补充文件
