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An oxidative alkylamination of 1,3,7-triazapyrenes in the aqueous medium

✍ Scribed by Ivan Borovlev; Oleg Demidov; Nadezhda Saigakova; Sergey Pisarenko; Olesya Nemykina


Publisher
Journal of Heterocyclic Chemistry
Year
2011
Tongue
English
Weight
101 KB
Volume
48
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

1,3,7‐Triazapyrene and 2‐methyl‐1,3,7‐triazapyrene have shown to react with a wide range of alkylamines in the presence of an oxidant (K~3~Fe(CN)~6~) in the water solution at room temperature to give rise to the corresponding 6‐mono‐alkyl(dialkyl)amino‐ and 6,8‐bis‐dialkylamino derivatives. J. Heterocyclic Chem., (2011).


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Kinetic study of the nitrosation of 1,3-
✍ Guillermo González-Alatorre; Salvador H. Guzmán-Maldonado; Eleazar M. Escamilla- 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 119 KB

## Abstract The kinetics of the nitrosation of 1,3‐dimethyl (DMU), 1,3‐diethyl (DEU), 1,3‐dipropylurea (DPU), 1,3‐dibuthyl (DBU), and 1,3‐diallylurea (DAU) were studied in a conventional UV/vis spectrophotometer in aqueous‐perchloric acid media. The kinetic study was carried out using the initial r