Pd-catalyzed intramolecular acylation of aryl bromides via C-H functionalization: A highly efficient synthesis of benzocyclobutenones
P. Álvarez-Bercedo, A. Flores-Gaspar, A. Correa, R. Martin
J. Am. Chem. Soc. 2010, 132, 466-467
Abstract: A new catalyst system for the intramolecular acylation of aldehydes with aryl bromides via C−H functionalization is described. The transformation is distinguished by a remarkable functional group tolerance and hence allows for the synthesis of a wide variety of highly functionalized benzocyclobutenones with a diverse set of substitution patterns from simple and easily accessible precursors.

 

  

Seminars

9/8/2010 12:00
Prof. Alan Katritzky
University of Florida (USA)
Some recent developments in the synthesis of peptides and peptide conjugates
9/3/2010 12:00
Prof. Jaume Vilarrassa
Universitat de Barcelona
Catalytic tricks

Publications

Zinc acetates as efficient catalysts for the synthesis of bis-isocyanate precursors
E. Reixach, N. Bonet, F. X. Rius-Ruiz, S. Wershofen, A. Vidal-Ferran
Ind. Eng. Chem. Res. 2010, 49, 6362-6366
Through-space ligand interactions in enantiomeric dinuclear Ru complexes
N. Planas, G. J. Christian, E. Mas-Marzá, X. Sala, X. Fontrodona, F. Maseras, A. Llobet
Chem. Eur. J. 2010, 16, 7965-7968
Interplay between carbon monoxide, hydrides, and carbides in selective alkyne hydrogenation on palladium
M. García-Mota, B. Bridier, J. Pérez-Ramírez, N. López
J. Catal. 2010, 273, 92-102

News & Events

7/9/2010
2010 ICIQ Summer Fellows

Education

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