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Pure Appl. Chem., 2004, Vol. 76, No. 3, pp. 679-688

http://dx.doi.org/10.1351/pac200476030679

Heterogeneous asymmetric catalysis

Marc Lemaire

Laboratoire de Catalyse et Synthese Organique UCBLCNRS, UMR 5622, CPE, 43 boul.11 Novembre, 69622 Villeurbanne Cédex, France

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  • Carreiro Elisabete P., Moura Nuno M. M., Burke Anthony J.: Covalent and Noncovalent Immobilization of Arylid-BOX Ligands and Their Derivatives: Evaluation in the Catalytic Asymmetric Cyclopropanation of Styrenes. Eur J Org 2012, 2012, 518. <http://dx.doi.org/10.1002/ejoc.201100781>
  • Ostrowski Sławomir, Jamróz Michał H., Rode Joanna E., Dobrowolski Jan Cz.: On Stability, Chirality Measures, and Theoretical VCD Spectra of the Chiral C58X2 Fullerenes (X = N, B). J Phys Chem A 2012, 116, 631. <http://dx.doi.org/10.1021/jp208687c>
  • Šebesta Radovan, Bilčík Filip: Imidazolium-tagged ferrocenyl diphosphanes in allylic substitution with heteroatom nucleophiles. Tet Asymm 2009, 20, 1892. <http://dx.doi.org/10.1016/j.tetasy.2009.07.039>
  • Wang Chao, Wu Xiaofeng, Xiao Jianliang: Broader, Greener, and More Efficient: Recent Advances in Asymmetric Transfer Hydrogenation. Chem. Asian J. 2008, 3, 1750. <http://dx.doi.org/10.1002/asia.200800196>
  • Indra Arindam, Basu Susmit, Kulkarni Dhanashree G., Gopinath Chinnakonda S., Bhaduri Sumit, Lahiri Goutam Kumar: MCM-41-supported ruthenium carbonyl cluster-derived catalysts for asymmetric hydrogenation reactions. CATAL A GENERAL 2008, 344, 124. <http://dx.doi.org/10.1016/j.apcata.2008.04.009>
  • He Xi Jun, Shen Zhen Lu, Mo Wei Min, Hu Bao Xiang, Sun Nan: Asymmetric Glyoxylate-Ene Reactions Catalyzed by Chiral Pd(II) Complexes in the Ionic Liquid [bmim][PF6]. IJMS 2007, 8, 553. <http://dx.doi.org/10.3390/i8060553>
  • Rodríguez Pilar, Caballero Ana, Díaz-Requejo M. Mar, Nicasio M. Carmen, Pérez Pedro J.: Very Efficient, Reusable Copper Catalyst for Carbene Transfer Reactions under Biphasic Conditions Using Ionic Liquids. Org Lett 2006, 8, 557. <http://dx.doi.org/10.1021/ol052564j>