Synthesis and antitumor activity of pyridoxine monoalkenyl derivatives


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Рұқсат жабық Тек жазылушылар үшін

Аннотация

A convenient method for the synthesis of pyridoxine alkenyl derivatives by the Wittig reaction of [(2,8-dimethyl-4H-[1,3]dioxino[4,5-c]pyridin-5-yl)methyl]triphenylphosphonium chloride with aldehydes was suggested. Some of the compounds obtained exhibit antitumor activity in vitro.

Авторлар туралы

T. Nguyen

Research and Education Center of Pharmacy, Kazan (Volga region) Federal University

Email: Yurii.Shtyrlin@gmail.com
Ресей, 18 ul. Kremlevskaya, Kazan, 420008

A. Iksanova

Research and Education Center of Pharmacy, Kazan (Volga region) Federal University

Email: Yurii.Shtyrlin@gmail.com
Ресей, 18 ul. Kremlevskaya, Kazan, 420008

O. Lodochnikova

A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center of the Russian Academy of Sciences

Email: Yurii.Shtyrlin@gmail.com
Ресей, 8 ul. Akad. Arbuzova, Kazan, 420088

Yu. Shtyrlin

Research and Education Center of Pharmacy, Kazan (Volga region) Federal University

Хат алмасуға жауапты Автор.
Email: Yurii.Shtyrlin@gmail.com
Ресей, 18 ul. Kremlevskaya, Kazan, 420008

M. Pugachev

Research and Education Center of Pharmacy, Kazan (Volga region) Federal University

Email: Yurii.Shtyrlin@gmail.com
Ресей, 18 ul. Kremlevskaya, Kazan, 420008

R. Pavelyev

Research and Education Center of Pharmacy, Kazan (Volga region) Federal University

Email: Yurii.Shtyrlin@gmail.com
Ресей, 18 ul. Kremlevskaya, Kazan, 420008

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