Phosphorylation of aminomalonates


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Аннотация

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.

Авторлар туралы

A. Egorova

St. Petersburg State Institute of Technology (Technical University); Scientific Research Center for Ecological Safety

Email: dog_alla@mail.ru
Ресей, Moskovskii pr. 26, St. Petersburg, 190013; St. Petersburg

N. Viktorov

St. Petersburg State Institute of Technology (Technical University)

Email: dog_alla@mail.ru
Ресей, Moskovskii pr. 26, St. Petersburg, 190013

D. Lyamenkova

St. Petersburg State Institute of Technology (Technical University)

Email: dog_alla@mail.ru
Ресей, Moskovskii pr. 26, St. Petersburg, 190013

N. Svintsitskaya

St. Petersburg State Institute of Technology (Technical University)

Email: dog_alla@mail.ru
Ресей, Moskovskii pr. 26, St. Petersburg, 190013

A. Garabadziu

St. Petersburg State Institute of Technology (Technical University)

Email: dog_alla@mail.ru
Ресей, Moskovskii pr. 26, St. Petersburg, 190013

A. Dogadina

St. Petersburg State Institute of Technology (Technical University)

Хат алмасуға жауапты Автор.
Email: dog_alla@mail.ru
Ресей, Moskovskii pr. 26, St. Petersburg, 190013

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