72889-91-9Relevant academic research and scientific papers
Synthesis and antifungal activity of N-(alkyl/aryl)-2-(3-oxo-1,4- benzothiazin-2-yl)acetamide
Gupta,Wagh
, p. 697 - 702 (2007/10/03)
A series of N-(alkyl/aryl)-2-(3-oxo-1,4-benzothiazin-2-yl)acetamide have been synthesized by condensation of substituted amines with maleic anhydride (MA) followed by cyclization with o-aminothiophenol (o-ATP). All the compounds have been screened for their antifungal activity against Tricophyton rubrum, Epidermophyton floccosum and Malassazia furfur. In the primary screening, some of the compounds exhibited appreciable activity. The structures of the synthesized compounds 7a-z have been established on the basis of elemental analysis and spectral data.
FACILE ESTERIFICATION OF CARBOXYLIC ACIDS WITH ORGANOPHOSPHORUS REAGENTS. NOVEL APPLICATION OF ALKYLPHOSPHORIC ESTERS (APE)
Balasubramaniyan, V.,Bhatia, V. G.,Wagh, S. B.
, p. 1475 - 1485 (2007/10/02)
A mixture of alkyl phosphate esters (APE) obtained from P4O10 and alkanols taken in 1:6 mole ratio is an excellent esterification reagent for several classes of carboxylic acids.This new reagent offers several advantages compared to conventional reagents.
Reactions of Cyclic Anhydrides: Part VI - Transesterification of Maleanilic and Fumaranilic Acids with Phosphorus Pentoxide-Alkanol
Wagh, S. B.,Balasubramaniyan, P.,Balasubramaniyan, V.
, p. 577 - 578 (2007/10/02)
Mixed phosphorus esters obtained from alkanols and phosphorus pentoxide furnish the corresponding esters in 80-90percent yield when refluxed with maleanilic and fumaranilic acids.
Reactions of Cyclic Anhydrides: Part V - Acid-catalysed Esterification of Maleanilic and Fumaranilic Acids and Evidence of Activation by Carboxamido Function
Patel, M. V.,Balasubramaniyan, V.
, p. 804 - 805 (2007/10/02)
Maleanilic and fumaranilic acids undergo acid catalysed esterification with methanol under very mild conditions.Intramolecular activation involving carboxamido group appears likely in this reactions.
