Synthesis and Antimicrobial Activity of 4-Hydroxy-2-[5-Nitrofuran(Thien)-2-Yl]-6h-1,3-Oxazin-6-Ones


Cite item

Full Text

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

Abstract

A series of new 4-hydroxy-6H-oxazin-6-ones containing 2-(5-nitrofuranyl) and 2-(5-nitrothienyl) moieties were obtained. New nitrofuran and thiophene derivatives were synthesized by reacting these oxazines with mono- (EtOH) and dinucleophiles (phenylhydrazine). It was established that the synthesized compounds possessed pronounced bactericidal activity against Staphylococcus aureus and, in some cases, Escherichia coli strains.

About the authors

N. M. Chernov

St. Petersburg State Chemical Pharmaceutical Academy

Author for correspondence.
Email: nikita.chernov@pharminnotech.com
Russian Federation, 14/A Ul. Prof. Popova, St. Petersburg, 197376

A. S. Koshevenko

St. Petersburg State Chemical Pharmaceutical Academy

Email: nikita.chernov@pharminnotech.com
Russian Federation, 14/A Ul. Prof. Popova, St. Petersburg, 197376

I. P. Yakovlev

St. Petersburg State Chemical Pharmaceutical Academy

Email: nikita.chernov@pharminnotech.com
Russian Federation, 14/A Ul. Prof. Popova, St. Petersburg, 197376

E. P. Anan’eva

St. Petersburg State Chemical Pharmaceutical Academy

Email: nikita.chernov@pharminnotech.com
Russian Federation, 14/A Ul. Prof. Popova, St. Petersburg, 197376

G. V. Ksenofontova

St. Petersburg State Chemical Pharmaceutical Academy

Email: nikita.chernov@pharminnotech.com
Russian Federation, 14/A Ul. Prof. Popova, St. Petersburg, 197376

A. E. Shchegolev

St. Petersburg State Chemical Pharmaceutical Academy

Email: nikita.chernov@pharminnotech.com
Russian Federation, 14/A Ul. Prof. Popova, St. Petersburg, 197376


Copyright (c) 2017 Springer Science+Business Media, LLC, part of Springer Nature

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies