Abstract
A synthetic route to 1,4-benzothiazine-2-carboxylic acid 1,1 -dioxides, analogues of the ‘fluoroquinolone’ family of antibacterials, has been developed; unfortunately, the target compound (the thia-analogue of pefloxacin) has not revealed remarkable antibacterial activity in vitro against the majority of the strains tested.
References
1.
10.1070/MC1993v003n04ABEH000267_bib1
Bouzard
Recent Advances in the Chemistry of Quinolones, Recent Progress in the Chemical Synthesis of Antibiotics,
1990
2.
10.1070/MC1993v003n04ABEH000267_bib2
The Quinolones,
1988
3.
10.1070/MC1993v003n04ABEH000267_bib3
The Quinolones,
1986
4.
10.1070/MC1993v003n04ABEH000267_bib4
Mokrushina
Zh. Vses. Khim. Ova im D. I. Mendeleeva,
1991
5.
Hubschwerlen C., Pflieger P., Specklin J.L., Gubernator K., Gmuender H., Angehrn P., Kompis I.
Journal of Medicinal Chemistry,
1992
6.
Seuter F., Fiedler V.B., Philipp E.
Cardiovascular Drug Reviews,
1986
7.
Cecchetti V., Fravolini A., Schiaffella F., Tabarrini O., Zhou W., Pagella P.G.
Journal of Heterocyclic Chemistry,
1992