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Reviews
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Reviews
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Angew. Chem. Int. Ed.
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Recent examples
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Recent examples
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Y.-B. Zhao, B. Mariampillai, D. A. Candito, B. Laleu, M. Z. Li, M. Lautens, Angew. Chem. 2009, 121, 1881-1884
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Angew. Chem.
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Zhao, Y.-B.1
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10
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Angew. Chem. Int. Ed. 2009, 48, 1849-1852
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Angew. Chem. Int. Ed.
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Angew. Chem. Int. Ed. 2009, 48, 6713-6716
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Angew. Chem. Int. Ed.
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M. Blanchot, D. A. Candito, F. Larnaud, M. Lautens, Org. Lett. 2011, 13, 1486-1489
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Org. Lett.
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Blanchot, M.1
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N. Della Ca, G. Maestri, M. Catellani, Chem. Eur. J. 2009, 15, 7850-7853.
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Chem. Eur. J.
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Della Ca, N.1
Maestri, G.2
Catellani, M.3
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79958010991
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For other computational studies, see
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G. Maestri, E. Motti, N. Della Ca, M. Malacria, E. Derat, M. Catellani, J. Am. Chem. Soc. 2011, 133, 8574-8585. For other computational studies, see
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J. Am. Chem. Soc.
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Motti, E.2
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Catellani, M.6
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D. J. Cárdenas, B. Martin-Matute, A. M. Echavarren, J. Am. Chem. Soc. 2006, 128, 5033-5040
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Cárdenas, D.J.1
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J. Vicente, A. Arcas, F. Juliá-Hernández, D. Bautista, Angew. Chem. 2011, 123, 7028-7031
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Angew. Chem.
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Angew. Chem. Int. Ed. 2011, 50, 6896-6899.
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Angew. Chem. Int. Ed.
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G. Maestri, M. H. Larraufie, E. Derat, C. Ollivier, L. Fensterbank, E. LacÃte, M. Malacria, Org. Lett. 2010, 12, 5692-5695.
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Angew. Chem. Int. Ed. 2011, 50, 12557-12261
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N. Della Ca, G. Maestri, M. Malacria, E. Derat, M. Catellani, Angew. Chem. 2011, 123, 12456-12469; Angew. Chem. Int. Ed. 2011, 50, 12557-12261.
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The outcome of the reaction is completely different from the one obtained by using o-bromobenzamides
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The outcome of the reaction is completely different from the one obtained by using o-bromobenzamides:, R. Ferraccioli, D. Carenzi, O. Rombola, M. Catellani, Org. Lett. 2004, 6, 4759-4762.
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a similar reactivity was observed with phenols, which are much more prone to dearomatization
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Angew. Chem. Int. Ed. 2011, 50, 4068-4093; a similar reactivity was observed with phenols, which are much more prone to dearomatization
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Angew. Chem. Int. Ed.
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0001933344
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for other reported pallado-catalyzed dearomatizations, see
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M. Catellani, F. Cugini, G. Bocelli, J. Organomet. Chem. 1999, 584, 63-67; for other reported pallado-catalyzed dearomatizations, see
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42
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73049088297
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For other examples of intermediate stabilization by water, see:, and references therein
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For other examples of intermediate stabilization by water, see:, S. Baumgarten, D. Lesage, V. Gandon, J.-P. Goddard, M. Malacria, J.-C. Tabet, Y. Gimbert, L. Fensterbank, ChemCatChem 2009, 1, 138-143, and references therein.
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ChemCatChem
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Baumgarten, S.1
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Fensterbank, L.8
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IV pathway was considered in the presence of water. Other potential pathways cannot be formally excluded at this stage
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IV pathway was considered in the presence of water. Other potential pathways cannot be formally excluded at this stage.
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Reviews
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Reviews
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83755181693
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Detailed computational results supporting our mechanistic rationalization in the dearomatization reaction are available in the Supporting Information
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Detailed computational results supporting our mechanistic rationalization in the dearomatization reaction are available in the Supporting Information.
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