Phosphorylation of aminomalonates
- Authors: Egorova A.V.1,2, Viktorov N.B.1, Lyamenkova D.V.1, Svintsitskaya N.I.1, Garabadziu A.V.1, Dogadina A.V.1
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Affiliations:
- St. Petersburg State Institute of Technology (Technical University)
- Scientific Research Center for Ecological Safety
- Issue: Vol 86, No 11 (2016)
- Pages: 2446-2453
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/216497
- DOI: https://doi.org/10.1134/S1070363216110086
- ID: 216497
Cite item
Abstract
The reactions of chloroethynylphosphonates with aromatic secondary aminomalonates occur as classic nucleophilic substitution of chlorine atom at the sp-hybridizied carbon atom to form new phosphorylated 2-arylaminomalonates, diethyl esters of 2-(diethoxyphosphorylethynyl)-2-arylaminomalonic acids. Nonobservance of chemo- and regioselectivity was revealed when using cyclohexyl- and benzylaminomalonates.
About the authors
A. V. Egorova
St. Petersburg State Institute of Technology (Technical University); Scientific Research Center for Ecological Safety
Email: dog_alla@mail.ru
Russian Federation, Moskovskii pr. 26, St. Petersburg, 190013; St. Petersburg
N. B. Viktorov
St. Petersburg State Institute of Technology (Technical University)
Email: dog_alla@mail.ru
Russian Federation, Moskovskii pr. 26, St. Petersburg, 190013
D. V. Lyamenkova
St. Petersburg State Institute of Technology (Technical University)
Email: dog_alla@mail.ru
Russian Federation, Moskovskii pr. 26, St. Petersburg, 190013
N. I. Svintsitskaya
St. Petersburg State Institute of Technology (Technical University)
Email: dog_alla@mail.ru
Russian Federation, Moskovskii pr. 26, St. Petersburg, 190013
A. V. Garabadziu
St. Petersburg State Institute of Technology (Technical University)
Email: dog_alla@mail.ru
Russian Federation, Moskovskii pr. 26, St. Petersburg, 190013
A. V. Dogadina
St. Petersburg State Institute of Technology (Technical University)
Author for correspondence.
Email: dog_alla@mail.ru
Russian Federation, Moskovskii pr. 26, St. Petersburg, 190013