1146702-35-3Relevant academic research and scientific papers
Synthesis and antimicrobial activity of substituted phenophosphazines
Lokhandwala,Desai
, p. 2678 - 2684 (2008)
Several Schiff base derivatives of phenophosphazines were synthesized by the reaction of amino phenophosphazines and aromatic aldehydes in equimolar ratio, using methanol as solvent. Possible structures have been proposed on the basis of elemental analysis, IR, and 1H NMR spectral studies. The antibacterial and antifungal activities of the above mentioned Schiff base derivatives have been evaluated against pathogens E. coli, S. typhi, S. aureus, B. subtilis, A. niger, and C. Albicans. Copyright Taylor & Francis Group, LLC.
Synthesis and antimicrobial activity of some phenophosphazines
Lokhandwala, Snehal,Desai
, p. 1366 - 1368 (2013/05/09)
A new family of organophosphorus compounds namely 3-chloro-1-(10-hydroxy- 10-oxo-5,10-dihydro-phenophosphazin-2-yl)-4-(substituted phenyl)-azetidin-2-one (3a-j) has been synthesized by reaction of 2-[(substituted benzylidene)-amino]- 10-oxo-5,10-dihydro-phenophosphazin-10-ol (2a-j) with chloro acetyl chloride and triethyl amine. All these compounds were characterized by elemental and spectral analysis. Their antimicrobial activity was also evaluated. Copyright
Novel organophosphorus compounds as potential antimicrobial agents
Lokhandwala,Desai
body text, p. 1264 - 1271 (2009/05/07)
The 4-Thiazolidinone derivatives of phenophosphazines were synthesized by a reaction of Schiff base derivative of phenophosphazine with Thyoglycollic acid in molar ratio of 1:3 using DMF as solvent. Possible structures have been proposed based on elemental analysis, IR and 1H NMR spectral studies. The antibacterial and antifungal activities of these derivatives have been evaluated against pathogens E. coli, S. typhi, S. aureus, B. subtilis, A. niger, and C. Albicans. Copyright Taylor & Francis Group, LLC.
