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Nickel-catalyzed amination of aryl pivalates by the cleavage of aryl C-O bonds.

Angewandte Chemie (International ed. in English) (2010-03-17)
Toshiaki Shimasaki, Mamoru Tobisu, Naoto Chatani
RÉSUMÉ

Catalytic amination: The title reaction demonstrates the use of aryl carboxylates as suitable electrophilic coupling substrates in catalytic amination reactions. N-heterocyclic carbene ligands and NaOtBu promote the amination of aryl pivalates through the cleavage of normally unreactive aryl carbon-oxygen bonds (see scheme; cod=cyclooctadiene).

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Sigma-Aldrich
Pivalic acid, 99%