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A new efficient deprotection of azines, hydrazones and oximes. An excellent route for exchanging oxygen isotopes in carbonyls
Authors:Mira Carmeli
Affiliation:School of Chemistry, Tel-Aviv University, Tel-Aviv 69978, Israel
Abstract:Carbonyls, protected as azines or other Cdouble bond; length as m-dashN derivatives can be deprotected by HOF·CH3CN in seconds to the corresponding ketone or aldehyde in very good yields. This reaction also offers a very efficient route for replacing the oxygen atom of most carbonyls with any other oxygen isotope, for example, [18]O.
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