: A palladium N-heterocyclic carbene catalyzed methodology for the synthesis of substituted, N-unprotected indoles and azaindoles is reported. The protocol permits access to various, highly substituted members of these classes of compounds. Although two possible reaction pathways (deprotonative and Heck-like) can be proposed, control experiments, supported by computational studies, point toward a deprotonative mechanism being operative.

Marelli, E., Corpet, M., Minenkov, Y., Neyyappadath, R.M., Bismuto, A., Buccolini, G., et al. (2016). Catalytic α-Arylation of Imines Leading to N-Unprotected Indoles and Azaindoles. ACS CATALYSIS, 6(5), 2930-2938 [10.1021/acscatal.6b00040].

Catalytic α-Arylation of Imines Leading to N-Unprotected Indoles and Azaindoles

Curcio, Massimiliano;
2016

Abstract

: A palladium N-heterocyclic carbene catalyzed methodology for the synthesis of substituted, N-unprotected indoles and azaindoles is reported. The protocol permits access to various, highly substituted members of these classes of compounds. Although two possible reaction pathways (deprotonative and Heck-like) can be proposed, control experiments, supported by computational studies, point toward a deprotonative mechanism being operative.
2016
Marelli, E., Corpet, M., Minenkov, Y., Neyyappadath, R.M., Bismuto, A., Buccolini, G., et al. (2016). Catalytic α-Arylation of Imines Leading to N-Unprotected Indoles and Azaindoles. ACS CATALYSIS, 6(5), 2930-2938 [10.1021/acscatal.6b00040].
Marelli, Enrico; Corpet, Martin; Minenkov, Yury; Neyyappadath, Rifahath M; Bismuto, Alessandro; Buccolini, Giulia; Curcio, Massimiliano; Cavallo, Luig...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/918137
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