Synthesis and antitumor activity of pyridoxine monoalkenyl derivatives


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription Access

Abstract

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.

About the authors

T. N. T. Nguyen

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

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

A. G. Iksanova

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

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

O. A. Lodochnikova

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

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

Yu. G. Shtyrlin

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

Author for correspondence.
Email: Yurii.Shtyrlin@gmail.com
Russian Federation, 18 ul. Kremlevskaya, Kazan, 420008

M. V. Pugachev

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

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

R. S. Pavelyev

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

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

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2016 Springer Science+Business Media New York