The full potential of a high valent metal chloride as both a chlorinating and an oxidative agent was explored by allowing WCl6 to react with N-(2,6-diisopropylphenyl) alpha-diimines, in CH2Cl2 at room temperature. These a-diimines underwent unprecedented conversion to quinoxalinium cations via intramolecular C-N coupling.

Bartalucci, N., Bortoluzzi, M., Funaioli, T., Marchetti, F., Pampaloni, G., Zacchini, S. (2017). Allowing the direct interaction of N-aryl α-diimines with a high valent metal chloride: one-pot WCl6-promoted formation of quinoxalinium salts. DALTON TRANSACTIONS, 46(38), 12780-12784 [10.1039/C7DT03226A].

Allowing the direct interaction of N-aryl α-diimines with a high valent metal chloride: one-pot WCl6-promoted formation of quinoxalinium salts

Zacchini, Stefano
2017

Abstract

The full potential of a high valent metal chloride as both a chlorinating and an oxidative agent was explored by allowing WCl6 to react with N-(2,6-diisopropylphenyl) alpha-diimines, in CH2Cl2 at room temperature. These a-diimines underwent unprecedented conversion to quinoxalinium cations via intramolecular C-N coupling.
2017
Bartalucci, N., Bortoluzzi, M., Funaioli, T., Marchetti, F., Pampaloni, G., Zacchini, S. (2017). Allowing the direct interaction of N-aryl α-diimines with a high valent metal chloride: one-pot WCl6-promoted formation of quinoxalinium salts. DALTON TRANSACTIONS, 46(38), 12780-12784 [10.1039/C7DT03226A].
Bartalucci, Niccolò; Bortoluzzi, Marco; Funaioli, Tiziana; Marchetti, Fabio; Pampaloni, Guido; Zacchini, Stefano
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/613481
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