This work discloses a strategy for the implementation of ON-ON organometallic catalytic processes using photoresponsive phosphine ligands. The approach leverages on the regiodivergent reactivity of mono- and bimetallic gold complexes that results from - vs -activations of alkynyl-substituted urea substrates, for the selective formation of eitherdihydroquinazolinone or indole-carboxamide products, via intramolecular hydroamidation.

Divergent Reactivity of E/Z‐Azobenzene‐Based Phosphine‐Gold Catalysts: Toward an ON‐ON Catalytic Photoswitch Process / N. Goual, S. Maisonneuve, F. Medici, P. Retailleau, J. Gallard, J. Xie, V. Gandon, A. Marinetti, A. Voituriez. - In: ADVANCED SYNTHESIS & CATALYSIS. - ISSN 1615-4150. - (2024), pp. 1-7. [Epub ahead of print] [10.1002/adsc.202401105]

Divergent Reactivity of E/Z‐Azobenzene‐Based Phosphine‐Gold Catalysts: Toward an ON‐ON Catalytic Photoswitch Process

F. Medici;
2024

Abstract

This work discloses a strategy for the implementation of ON-ON organometallic catalytic processes using photoresponsive phosphine ligands. The approach leverages on the regiodivergent reactivity of mono- and bimetallic gold complexes that results from - vs -activations of alkynyl-substituted urea substrates, for the selective formation of eitherdihydroquinazolinone or indole-carboxamide products, via intramolecular hydroamidation.
Photoresponsive phosphines; azobenzenes; triazonines; gold catalysis; regiodivergency
Settore CHEM-05/A - Chimica organica
2024
16-ott-2024
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1114369
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