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Pure Appl. Chem., 1998, Vol. 70, No. 5, pp. 1123-1128

http://dx.doi.org/10.1351/pac199870051123

New catalysts and methods for highly enantioselective metal carbene reactions

M. P. Doyle

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  • Zhang Min, Guo Junkai, Gong Yuefa: Highly Regioselective Cascade Formal Nucleophilic Substitution and Aldol Condensation of 2-Aroyl-1-chlorocyclopropanecarboxylic Esters. Eur. J. Org. Chem. 2014, 2014, 1942. <http://dx.doi.org/10.1002/ejoc.201301866>
  • McMills Mark C., Humes Ross J., Pavlyuk Oksana M.: Catalytic enantioselective synthesis of azacycloalkenes via intermolecular rhodium carbenoid C–H insertion/ring-closing metathesis sequence. Tetrahedron Letters 2012, 53, 849. <http://dx.doi.org/10.1016/j.tetlet.2011.12.019>
  • Jarrahpour Aliasghar, Ebrahimi Edris, De Clercq Erik, Sinou Véronique, Latour Christine, Djouhri Bouktab Lamia, Brunel Jean Michel: Synthesis of mono-, bis-spiro- and dispiro-β-lactams and evaluation of their antimalarial activities. Tedrahedron 2011, 67, 8699. <http://dx.doi.org/10.1016/j.tet.2011.09.041>
  • Briones John F., Davies Huw M. L.: Silver Triflate-Catalyzed Cyclopropenation of Internal Alkynes with Donor-/Acceptor-Substituted Diazo Compounds. Org Lett 2011, 13, 3984. <http://dx.doi.org/10.1021/ol201503j>
  • Majumdar Moumita, Sinha Arup, Ghatak Tapas, Patra Sanjib K., Sadhukhan Nabanita, Rahaman S. M. Wahidur, Bera Jitendra K.: Mapping the Transformation [{RuII(CO)3Cl2}2]→[RuI 2(CO)4]2+: Implications in Binuclear Water-Gas Shift Chemistry. Chem Eur J 2010, 16, 2574. <http://dx.doi.org/10.1002/chem.200902797>
  • DOYLE M. P.: ChemInform Abstract: New Catalysts and Methods for Highly Enantioselective Metal Carbene Reactions. ChemInform 2010, 29, no. <http://dx.doi.org/10.1002/chin.199851336>
  • Omae Iwao: Characteristic reactions of group 9 transition metal compounds in organic synthesis. Appl Organometal Chem 2009, 23, 91. <http://dx.doi.org/10.1002/aoc.1480>
  • Trabocchi Andrea, Lalli Claudia, Guarna Francesco, Guarna Antonio: Diastereoselective Synthesis of Highly Constrained Spiro-β-Lactams by the Staudinger Reaction Using an Unsymmetrical Bicyclic Ketene. Eur J Org Chem 2007, 2007, 4594. <http://dx.doi.org/10.1002/ejoc.200700260>
  • Harned Andrew M., Sherrill W. Matthew, Flynn Daniel L., Hanson Paul R.: High-load, soluble oligomeric benzenesulfonyl azide: application to facile diazo-transfer reactions. Tetrahedron 2005, 61, 12093. <http://dx.doi.org/10.1016/j.tet.2005.08.120>
  • Simonneaux Gérard, Galardon Erwan, Paul-Roth Christine, Gulea Mihaela, Masson Serge: Ruthenium–porphyrin-catalyzed carbenoid addition to allylic compounds: application to [2,3]-sigmatropic rearrangements of ylides. J Organomet Chem 2001, 617-618, 360. <http://dx.doi.org/10.1016/S0022-328X(00)00635-5>
  • Colacot Thomas J.: An overview on the applications of ‘Doyle catalysts’ in asymmetric cyclopropanation, cyclopropenation and C-H insertion reactions. J Chem Sci 2000, 112, 197. <http://dx.doi.org/10.1007/BF02706172>
  • Rigby James H., Cavezza Alexandre, Heeg Mary Jane: Asymmetric induction in [1+4] cycloadditions of vinyl isocyanates with chiral nucleophilic carbenes. Tetrahetron Lett 1999, 40, 2473. <http://dx.doi.org/10.1016/S0040-4039(99)00280-4>