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Pure Appl. Chem., 2008, Vol. 80, No. 5, pp. 861-871

http://dx.doi.org/10.1351/pac200880050861

Ruthenium catalysts for selective nucleophilic allylic substitution

Christian Bruneau, Jean-Luc Renaud and Bernard Demerseman

UMR 6226, CNRS-Université de Rennes 1: Sciences Chimiques de Rennes, Catalyse et Organométalliques, Campus de Beaulieu-35042 Rennes Cedex, France

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  • Bruneau Christian, Achard Mathieu: Allylic ruthenium(IV) complexes in catalysis. Coord Rev 2011. <http://dx.doi.org/10.1016/j.ccr.2011.10.018>
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  • Štambaský Jan, Kapras Vojtěch, Štefko Martin, Kysilka Ondřej, Hocek Michal, Malkov Andrei V., Kočovský Pavel: A Modular Approach to Aryl-C-ribonucleosides via the Allylic Substitution and Ring-Closing Metathesis Sequence. A Stereocontrolled Synthesis of All Four α-/β- and d-/l-C-Nucleoside Stereoisomers. J Org Chern 2011, 76, 7781. <http://dx.doi.org/10.1021/jo201110z>
  • Brancatelli Giovanna, Drommi Dario, Feminò Giusy, Saporita Maria, Bottari Giovanni, Faraone Felice: Basicity and bulkiness effects of 1,8-diaminonaphthalene, 8-aminoquinoline and their alkylated derivatives on the different efficiencies of η5-C5H5 and η5-C5Me5 ruthenium precatalysts in allylic etherification reactions. New J Chem 2010, 34, 2853. <http://dx.doi.org/10.1039/c0nj00338g>
  • Saporita Maria, Bottari Giovanni, Bruno Giuseppe, Drommi Dario, Faraone Felice: Regio- and enantioselectivity in the alkylation and etherification reactions of cinnamyl allylic derivatives catalyzed by [(η5-C5R5)Ru(N–N*)(NCCH3)]PF6 (R=H, Me) complexes containing N–N* bulky chiral ligands of different rigidity and flexibility. Journal of Molecular Catalysis A 2009, 309, 159. <http://dx.doi.org/10.1016/j.molcata.2009.05.011>
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