The synthesis of organic compounds using aqueous medium has become an indispensable
tool for modern chemical synthesis strategies because of its ability to produce pure products …

Surfactant/I2/Water: An Efficient System for Deprotection of Oximes and Imines to Carbonyls
under Neutral Conditions in Water | The Journal of Organic Chemistry Recently Viewedclose …

Highly efficient oxidation of oximes to carbonyl compounds by molecular oxygen with
benzaldehyde as an oxygen acceptor in the presence of metalloporphyrins has been …

Analogues of the natural product collismycin bearing a carboxylic acid moiety has been
efficiently synthesised from several collismycin precursors through a laccase-catalysed …

Sym-collidinium chlorochromate (S-COCC), is a new, rapid and useful reagent for the
oxidative deprotection of oximes to the corresponding carbonyl compounds. The interesting …

The deprotection of wide varieties of oximes, imines, and azines to their corresponding
carbonyls has been achieved using Cu-nanoparticles on a cellulose template as a reusable …

Following the previous review of the same title and authors, this up-date deals with the
research progress in regeneration of carbonyl compounds from oximes starting from 2001 …

Use of trimethylphosphine (Me3P) and 2, 2′-dipyridyl diselenide (PySeSePy) is an
excellent method for the conversion of ketoximes to the corresponding ketones, since yields …

Toward new camptothecins. Part 5: On the synthesis of precursors for the crucial
Friedländer reaction - ScienceDirect Skip to main contentSkip to article Elsevier logo …