Data di Pubblicazione:
2016
Citazione:
Mild AgOTf Catalyzed Synthesis of 1-Carbosubstituted-isochromenes / G. Abbiati, M. Dell’Acqua, S. Peroni, V. Pirovano, E. Rossi - In: Congresso delle sezioni Toscana-Umbria-Marche-Abruzzo della società chimica italiana[s.l] : Società chimica italiana, 2016 Sep 26. - ISBN 9788886208789. - pp. 78-78 (( Intervento presentato al 35. convegno TUMA tenutosi a Giulianova nel 2016.
Abstract:
One of the most efficient methods for the construction of 1-substituted isochromenes (and related heteroaryl compounds such as pyrano[4,3-b]pyridines) is the metal catalyzed regioselective domino cycloisomerization/nucleophilic addition reaction of a properly substituted 2-alkynyl(hetero)arylaldehyde in the presence of a suitable nucleophile. The reaction with oxygen nucleophiles is the most studied and several metal catalyst, i.e., Pd(II), Cu(I), Ag(I), Au(I) and In(III), demonstrated to be effective for synthesis of 1-alkoxyisochromenes. Conversely, the reaction with carbon nucleophiles, and in particular with enolizable carbonyl compounds, is relatively less investigated. In connection with our ongoing interest in the development of silver catalysed domino approaches involving alkyne derivatives, we report here a silver catalyzed domino approach to isochromenes starting from 2-alkynyl(hetero)arylaldehydes and enolizable carbonyl compounds. The reaction yields range from fair to very good. The reaction mechanism is also investigated and the formation of by-products discussed.
Tipologia IRIS:
03 - Contributo in volume
Keywords:
silver; domino reaction; isochromenes; alkynylbenzaldehydes; carbon nucleophiles; enolisable carbonyl compounds
Elenco autori:
G. Abbiati, M. Dell’Acqua, S. Peroni, V. Pirovano, E. Rossi
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Titolo del libro:
Congresso delle sezioni Toscana-Umbria-Marche-Abruzzo della società chimica italiana