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   <subfield code="a">Super acid catalysed sequential hydrolysis/cycloisomerization of o -(acetylenic)benzamides under microwave condition: Synthesis, antinociceptive and antiinflammatory activity of substituted isocoumarins</subfield>
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   <subfield code="a">Synthesis of isocoumarins and related compounds via triflic acid promoted hydrolysis/cyclization sequence of 2-(alkynyl)benzamides under microwave condition was achieved. The substrate scope of the reaction was broad to include not only aromatic but also polyaromatic and heteroaromatic motifs, thus highlighting the significance of this methodology. One-pot operation, short reaction time, good chemical yields and excellent regioselectivity are the advantages of this protocol. All the synthesized compounds were evaluated for their antinociceptive and antiinflammatory activities using in vivo rodent models. Graphical Abstract Synthesis of isocoumarins via triflic acid promoted sequential hydrolysis/cyclization of 2-(alkynyl)benzamides under microwave condition was achieved. All the synthesized compounds were evaluated for their antinociceptive and antiinflammatory activities using in vivo rodent models.</subfield>
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