Synthesis and antitumor activity of pyridoxine monoalkenyl derivatives


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Resumo

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.

Sobre autores

T. Nguyen

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

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

A. Iksanova

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

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

Yu. Shtyrlin

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

Autor responsável pela correspondência
Email: Yurii.Shtyrlin@gmail.com
Rússia, 18 ul. Kremlevskaya, Kazan, 420008

M. Pugachev

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

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

R. Pavelyev

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

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

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