Pure and Applied Chemistry

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• Raynal Matthieu, Ballester Pablo, Vidal-Ferran Anton, van Leeuwen Piet W. N. M.: Supramolecular catalysis. Part 1: non-covalent interactions as a tool for building and modifying homogeneous catalysts. Chem. Soc. Rev. 2014, 43, 1660. <http://dx.doi.org/10.1039/c3cs60027k>
• Besset Tatiana, Norman David W., Reek Joost N. H.: Supramolecular Encapsulated Rhodium Catalysts for Branched Selective Hydroformylation of Alkenes at High Temperature. Adv. Synth. Catal. 2013, n/a. <http://dx.doi.org/10.1002/adsc.201200790>
• Dydio Paweł, Breuil Pierre-Alain R., Reek Joost N. H.: Dynamic Combinatorial Chemistry in Chemical Catalysis. Isr. J. Chem. 2013, 53, 61. <http://dx.doi.org/10.1002/ijch.201200083>
• Udvardy Antal, Bényei Attila Csaba, Juhász Péter, Joó Ferenc, Kathó Ágnes: Two in one: Charged tertiary phosphines held together by ionic or covalent interactions as bidentate phosphorus ligands for synthesis of half-sandwich Ru(II)-complexes. Polyhedron 2013, 60, 1. <http://dx.doi.org/10.1016/j.poly.2013.05.008>
• Dydio Paweł, Detz Remko J., Reek Joost N. H.: Precise Supramolecular Control of Selectivity in the Rh-Catalyzed Hydroformylation of Terminal and Internal Alkenes. J. Am. Chem. Soc. 2013, 135, 10817. <http://dx.doi.org/10.1021/ja4046235>
• Anselmo Daniele, Gramage-Doria Rafael, Besset Tatiana, Escárcega-Bobadilla Martha V., Salassa Giovanni, Escudero-Adán Eduardo C., Martínez Belmonte Marta, Martin Eddy, Reek Joost N. H., Kleij Arjan W.: Supramolecular bulky phosphines comprising 1,3,5-triaza-7-phosphaadamantane and Zn(salphen)s: structural features and application in hydrosilylation catalysis. Dalton Trans. 2013, 42, 7595. <http://dx.doi.org/10.1039/c3dt00078h>
• Núñez-Rico José L., Etayo Pablo, Fernández-Pérez Héctor, Vidal-Ferran Anton: Modular POP Ligands in Rhodium-Mediated Asymmetric Hydrogenation: A Comparative Catalysis Study. Adv. Synth. Catal. 2012, 354, 3025. <http://dx.doi.org/10.1002/adsc.201200477>
• Pignataro Luca, Boghi Michele, Civera Monica, Carboni Stefano, Piarulli Umberto, Gennari Cesare: Rhodium-Catalyzed Asymmetric Hydrogenation of Olefins with PhthalaPhos, a New Class of Chiral Supramolecular Ligands. Chemistry A European Journal 2012, 18, 1383. <http://dx.doi.org/10.1002/chem.201102018>
• Pignataro Luca, Bovio Chiara, Civera Monica, Piarulli Umberto, Gennari Cesare: A Library Approach to the Development of BenzaPhos: Highly Efficient Chiral Supramolecular Ligands for Asymmetric Hydrogenation. Chem. Eur. J. 2012, 18, 10368. <http://dx.doi.org/10.1002/chem.201201032>
• Ohmatsu Kohsuke, Ito Mitsunori, Kunieda Tomoatsu, Ooi Takashi: Ion-paired chiral ligands for asymmetric palladium catalysis. Nature Chem 2012, 4, 473. <http://dx.doi.org/10.1038/nchem.1311>
• Dydio Paweł, Dzik Wojciech I., Lutz Martin, de Bruin Bas, Reek Joost N. H.: Remote Supramolecular Control of Catalyst Selectivity in the Hydroformylation of Alkenes. Angew Chem 2011, 123, 416. <http://dx.doi.org/10.1002/ange.201005173>
• Dydio Paweł, Dzik Wojciech I., Lutz Martin, de Bruin Bas, Reek Joost N. H.: Remote Supramolecular Control of Catalyst Selectivity in the Hydroformylation of Alkenes. Angew Chem Int Ed 2011, 50, 396. <http://dx.doi.org/10.1002/anie.201005173>
• Dydio Paweł, Rubay Christophe, Gadzikwa Tendai, Lutz Martin, Reek Joost N. H.: “Cofactor”-Controlled Enantioselective Catalysis. S J Am Chem Soc 2011, 133, 17176. <http://dx.doi.org/10.1021/ja208589c>
• Carboni Stefano, Gennari Cesare, Pignataro Luca, Piarulli Umberto: Supramolecular ligand–ligand and ligand–substrate interactions for highly selective transition metal catalysis. Dalton Trans 2011, 40, 4355. <http://dx.doi.org/10.1039/c0dt01517b>
• Pignataro Luca, Carboni Stefano, Civera Monica, Colombo Raffaele, Piarulli Umberto, Gennari Cesare: PhthalaPhos: Chiral Supramolecular Ligands for Enantioselective Rhodium-Catalyzed Hydrogenation Reactions. Angew Chem 2010, 122, 6783. <http://dx.doi.org/10.1002/ange.201002958>
• Pignataro Luca, Carboni Stefano, Civera Monica, Colombo Raffaele, Piarulli Umberto, Gennari Cesare: PhthalaPhos: Chiral Supramolecular Ligands for Enantioselective Rhodium-Catalyzed Hydrogenation Reactions. Angew Chem Int Ed 2010, 49, 6633. <http://dx.doi.org/10.1002/anie.201002958>
• Breuil Pierre-Alain R., Patureau Frederic W., Reek Joost N. H.: Singly Hydrogen Bonded Supramolecular Ligands for Highly Selective Rhodium-Catalyzed Hydrogenation Reactions. Angew Chem 2009, 121, 2196. <http://dx.doi.org/10.1002/ange.200806177>
• Breuil Pierre-Alain R., Patureau Frederic W., Reek Joost N. H.: Singly Hydrogen Bonded Supramolecular Ligands for Highly Selective Rhodium-Catalyzed Hydrogenation Reactions. Angew Chem Int Ed 2009, 48, 2162. <http://dx.doi.org/10.1002/anie.200806177>
• Pignataro Luca, Lynikaite Benita, Cvengroš Ján, Marchini Mattia, Piarulli Umberto, Gennari Cesare: Combinations of Acidic and Basic Monodentate Binaphtholic Phosphites as Supramolecular Bidentate Ligands for Enantioselective Rh-Catalyzed Hydrogenations. Eur J Org Chem 2009, 2009, 2539. <http://dx.doi.org/10.1002/ejoc.200900158>
• Breuil Pierre-Alain R., Reek Joost N. H.: Amino Acid Based Phosphoramidite Ligands for the Rhodium-Catalyzed Asymmetric Hydrogenation. Eur J Org Chem 2009, 2009, 6225. <http://dx.doi.org/10.1002/ejoc.200901044>
• Goudriaan P. Elsbeth, Kuil Mark, Jiang Xiao-Bin, van Leeuwen Piet W. N. M., Reek Joost N. H.: SUPRAPhos ligands for the regioselective rhodium catalyzed hydroformylation of styrene forming the linear aldehyde. Dalton Trans 2009, 1801. <http://dx.doi.org/10.1039/b818665k>
• Rubio Miguel, Jellema Erica, Siegler Maxime A., Spek Anthony L., Reek Joost N. H., de Bruin Bas: Supramolecular NHC ligands: on the influence of ZnII-templates on the activity of RhI(cod) complexes in ‘carbene polymerization’. Dalton Trans 2009, 8970. <http://dx.doi.org/10.1039/b911339h>
• Uraguchi D., Ueki Y., Ooi T.: Chiral Organic Ion Pair Catalysts Assembled Through a Hydrogen-Bonding Network. Sceince 2009, 326, 120. <http://dx.doi.org/10.1126/science.1176758>
• Breit Bernhard: ChemInform Abstract: Catalysts Through Self-Assembly for Combinatorial Homogeneous Catalysis. ChemInform 2008, 39. <http://dx.doi.org/10.1002/chin.200843254>