Abstract
This article has no abstract. Keywords: preparation; comparison with lead tetraacetate; oxidation; sulfoxides; oxidative cyclization; o-quinones; review; α-methoxy-α-arylacetic acid esters; dimethyl acetals; oxidation of enones; coumarane-3-ones; vic-triketones; cleavage of terminal tyrosyl and tryptophanyl peptides; diphenylmethyl (benzhydryl) esters; 1,4-epimines; oxidation of phenols; diimide from hydrazine hydrate; alkynyl carboxylates; cyclic acetals; iododecarboxylation; oxidative rearrangement of aryl methyl ketones; oxidation of N-protected tyrosine; diaryliodonium triflates; oxidation of phenols; cleavage of azones; methyl carbamates; 2-aryl-4-quinolones and 3-hydroxyflavones; phenyl alkynyl selenides; bridgehead functionalization; diaryltelluronium diacetates; oxidative heterocyclizations; dibenzocyclooctene lignans; 1,2-dithiocyanatoalkanes; oxidative displacement of propargylic silanes; mixed iodonium salts; oxidations; oxidation of hydrazides leads to N,N′-diacylhydrazines; hofmann rearrangement; difunctionalization of alkenes; diaryliodonium sulfonates; oxidations; ring contraction; benzyne precursors; N-sulfonylamine activation; amination; oxidations; heterocycles; acetoxy transfer; oxidations; cycloaddition; preparation; oxidation; nitrenes; azodicarboxylates; directed acetoxylation; S-imines; alkenyl iodonium salts; analogue; generation of electrophilic halogen; oxidative functionalization; phenol oxidation; oxidation of nitrogenous compounds; oxidation at carbon sites; new reagents; halogenation
Published Version
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