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J Org Chem ; 79(22): 10988-98, 2014 Nov 21.
Article in English | MEDLINE | ID: mdl-25343572

ABSTRACT

A metal-free oxidative cycloaddition reaction of substituted benzamides and alkynes has been developed for the synthesis of isoquinolones by using bis(trifluoracetoxy)iodobenzene (PIFA) and trifluoroacetic acid (TFA). Under mild conditions, a wide variety of isoquinolones were conveniently prepared via oxidative annulation of simple N-methoxybenzamide and diarylacetylene or aryl/alkyl acetylene derivatives in yields up to 87%.


Subject(s)
Alkynes/chemistry , Iodine/chemistry , Iodobenzenes/chemistry , Isoquinolines/chemistry , Isoquinolines/chemical synthesis , Metals/chemistry , Trifluoroacetic Acid/chemistry , Catalysis , Cycloaddition Reaction , Molecular Structure , Oxidation-Reduction
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