Vinyl-substituted 1,4-benzodiazepinones were obtained in good yields (10 examples, 61-82% yield) via the reaction between N-allenyl anthranyl amides and aryl iodides under Pd(0) catalysis. This new single cycle catalytic domino transformation involves a C-C followed by an N-C bond formation.

Synthesis of 1,4-benzodiazepinones via palladium-catalysed allene carbopalladation/amination domino sequence

BROGGINI, GIANLUIGI;
2014-01-01

Abstract

Vinyl-substituted 1,4-benzodiazepinones were obtained in good yields (10 examples, 61-82% yield) via the reaction between N-allenyl anthranyl amides and aryl iodides under Pd(0) catalysis. This new single cycle catalytic domino transformation involves a C-C followed by an N-C bond formation.
2014
1,4-Benzodiazepinones; Allene; Amination; Carbopalladation; Domino reactions; Palladium
Rigamonti, M.; Prestat, G.; Broggini, Gianluigi; Poli, G.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11383/2019502
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