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Gooßen, Lukas J., Rudolphi, Felix, Oppel, Christoph, Rodríguez, Nuria (2008) Synthesis of Ketones from α-Oxocarboxylates and Aryl Bromides by Cu/Pd-Catalyzed Decarboxylative Cross-Coupling. Angewandte Chemie International Edition, 47 (16). 3043-3045 doi:10.1002/anie.200705127

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Reference TypeJournal (article/letter/editorial)
TitleSynthesis of Ketones from α-Oxocarboxylates and Aryl Bromides by Cu/Pd-Catalyzed Decarboxylative Cross-Coupling
JournalAngewandte Chemie International Edition
AuthorsGooßen, Lukas J.Author
Rudolphi, FelixAuthor
Oppel, ChristophAuthor
Rodríguez, NuriaAuthor
Year2008 (April 7)Volume47
Issue16
PublisherWiley
DOIdoi:10.1002/anie.200705127Search in ResearchGate
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Mindat Ref. ID8584375Long-form Identifiermindat:1:5:8584375:2
GUID0
Full ReferenceGooßen, Lukas J., Rudolphi, Felix, Oppel, Christoph, Rodríguez, Nuria (2008) Synthesis of Ketones from α-Oxocarboxylates and Aryl Bromides by Cu/Pd-Catalyzed Decarboxylative Cross-Coupling. Angewandte Chemie International Edition, 47 (16). 3043-3045 doi:10.1002/anie.200705127
Plain TextGooßen, Lukas J., Rudolphi, Felix, Oppel, Christoph, Rodríguez, Nuria (2008) Synthesis of Ketones from α-Oxocarboxylates and Aryl Bromides by Cu/Pd-Catalyzed Decarboxylative Cross-Coupling. Angewandte Chemie International Edition, 47 (16). 3043-3045 doi:10.1002/anie.200705127
In(2008, April) Angewandte Chemie International Edition Vol. 47 (16) Wiley

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Gooßen, Lukas J., Rudolphi, Felix, Oppel, Christoph, Rodríguez, Nuria (2008) Synthese von Ketonen aus α-Oxocarboxylaten und Arylbromiden durch Cu/Pd-katalysierte decarboxylierende Kreuzkupplung. Angewandte Chemie, 120 (16). 3085-3088 doi:10.1002/ange.200705127
Rodríguez, Nuria, Manjolinho, Filipe, Grünberg, Matthias F., Gooßen, Lukas J. (2011) Synthesis of α,β-Unsaturated Ketones by Pd-Catalyzed Decarboxylative Allylation of α-Oxocarboxylates. Chemistry - A European Journal, 17 (49). 13688-13691 doi:10.1002/chem.201102584
Gooßen, Lukas J., Zimmermann, Bettina, Knauber, Thomas (2008) Palladium/Copper-Catalyzed Decarboxylative Cross-Coupling of Aryl Chlorides with Potassium Carboxylates. Angewandte Chemie International Edition, 47 (37). 7103-7106 doi:10.1002/anie.200800728
Gooßen, Lukas J., Rodríguez, Nuria, Lange, Paul P., Linder, Christophe (2010) Decarboxylative Cross-Coupling of Aryl Tosylates with Aromatic Carboxylate Salts. Angewandte Chemie International Edition, 49 (6). 1111-1114 doi:10.1002/anie.200905953
Gooßen, Lukas J., Rodríguez, Nuria, Gooßen, Käthe (2008) Carboxylic Acids as Substrates in Homogeneous Catalysis. Angewandte Chemie International Edition, 47 (17). 3100-3120 doi:10.1002/anie.200704782
Gooßen, Lukas J., Lange, Paul P., Rodríguez, Nuria, Linder, Christophe (2010) Low-Temperature Ag/Pd-Catalyzed Decarboxylative Cross-Coupling of Aryl Triflates with Aromatic Carboxylate Salts. Chemistry - A European Journal, 16 (13). 3906-3909 doi:10.1002/chem.200903319
Gooßen, Lukas J., Rodríguez, Nuria, Gooßen, Käthe (2009) Stereoselective Synthesis of β-Chlorovinyl Ketones and Arenes by the Catalytic Addition of Acid Chlorides to Alkynes. Angewandte Chemie International Edition, 48 (51). 9592-9594 doi:10.1002/anie.200904615
Gooßen, Lukas J., Rodríguez, Nuria, Lange, Paul P., Linder, Christophe (2010) Decarboxylative Cross-Coupling of Aryl Tosylates with Aromatic Carboxylate Salts. Angewandte Chemie, 122 (6). 1129-1132 doi:10.1002/ange.200905953
Gooßen, Lukas J., Rodríguez, Nuria, Gooßen, Käthe (2008) Cover Picture: Carboxylic Acids as Substrates in Homogeneous Catalysis (Angew. Chem. Int. Ed. 17/2008). Angewandte Chemie International Edition, 47 (17). 3067 doi:10.1002/anie.200890073
Song, Bingrui, Knauber, Thomas, Gooßen, Lukas J. (2013) Decarboxylative Cross-Coupling of Mesylates Catalyzed by Copper/Palladium Systems with Customized Imidazolyl Phosphine Ligands. Angewandte Chemie International Edition, 52 (10). 2954-2958 doi:10.1002/anie.201208025
Biafora, Agostino, Krause, Thilo, Hackenberger, Dagmar, Belitz, Florian, Gooßen, Lukas J. (2016) ortho -C−H Arylation of Benzoic Acids with Aryl Bromides and Chlorides Catalyzed by Ruthenium. Angewandte Chemie International Edition, 55 (47). 14752-14755 doi:10.1002/anie.201607270
 
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