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Pure Appl. Chem., 2001, Vol. 73, No. 7, pp. 1075-1086

http://dx.doi.org/10.1351/pac200173071075

Recent applications of tricarbonyliron-diene complexes to organic synthesis

Hans-Joachim Knölker, Arnold Braier, Dirk J. Bröcher, Simon Cämmerer, Wolfgang Fröhner, Peter Gonser, Holger Hermann, Daniela Herzberg, Kethiri R. Reddy and Guy Rohde

Institut für Organische Chemie, Universität Karlsruhe, Richard-Willstätter-Allee, 76131 Karlsruhe, Germany

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  • Murru Siva, Srivastava Radhey S.: Iron-Catalyzed Allylic C-H Amination of Substituted 1,3-Dienes. Eur. J. Org. Chem. 2014, 2014, 2174. <http://dx.doi.org/10.1002/ejoc.201301914>
  • Hesse Ronny, Gruner Konstanze K., Kataeva Olga, Schmidt Arndt W., Knölker Hans-Joachim: Efficient Construction of Pyrano[3,2-a ]carbazoles: Application to a Biomimetic Total Synthesis of Cyclized Monoterpenoid Pyrano[3,2-a ]carbazole Alkaloids. Chem. Eur. J. 2013, 19, 14098. <http://dx.doi.org/10.1002/chem.201301792>
  • Chase Hilary M., McDonough Thomas J., Overly Kenneth R., Laperle Christopher M.: Combined 1 H NMR and DFT study of the solvent effects on the iron pentacarbonyl-catalyzed photo-assisted isomerization of allyl alcohol. J. Phys. Org. Chem. 2013, 26, 322. <http://dx.doi.org/10.1002/poc.3091>
  • Ali Khan Monika, Mahon Mary F., Lowe John P., Stewart Alan J. W., Lewis Simon E.: Valuable New Cyclohexadiene Building Blocks from Cationic η5 -Iron-Carbonyl Complexes Derived from a Microbial Arene Oxidation Product. Chem. Eur. J. 2012, 18, 13480. <http://dx.doi.org/10.1002/chem.201202411>
  • Stephenson G. Richard, Anson Christopher E., Malkov Andrei V., Roe Caroline: Influencing the Balance between ipso and ω Nucleophile Addition to (1-Arylcyclohexadienyl)iron Intermediates in Alkaloid Synthesis. Eur. J. Org. Chem. 2012, 2012, 4716. <http://dx.doi.org/10.1002/ejoc.201200687>
  • Schmidt Arndt W., Reddy Kethiri R., Knölker Hans-Joachim: Occurrence, Biogenesis, and Synthesis of Biologically Active Carbazole Alkaloids. Chem. Rev. 2012, 112, 3193. <http://dx.doi.org/10.1021/cr200447s>
  • Stephenson G. Richard, Roe Caroline, Sandoe Elizabeth J.: Electrophilic C12 Building Blocks for Alkaloids: 1,1 Iterative Organoiron-Mediated Routes to (±)-Lycoramine and (±)-Maritidine. Eur J Org Chem 2011, 2011, 1664. <http://dx.doi.org/10.1002/ejoc.201001394>
  • Forke Ronny, Gruner Konstanze K., Knott Kerstin E., Auschill Stefan, Agarwal Sameer, Martin René, Böhl Markus, Richter Sabine, Tsiavaliaris Georgios, Fedorov Roman: Total synthesis of biologically active alkaloids using transition metals. Pure and App Chemis 2010, 1. <http://dx.doi.org/10.1351/PAC-CON-09-12-15>
  • Knölker Hans-Joachim: Synthesis of Biologically Active Carbazole Alkaloids Using Selective Transition-metal-catalyzed Coupling Reactions. Chem Lett 2009, 38, 8. <http://dx.doi.org/10.1246/cl.2009.8>
  • Anson Christopher E., Malkov Andrei V., Roe Caroline, Sandoe Elizabeth J., Stephenson G. Richard: Stereomanipulation of (η5-1-Arylcyclohexadienyl)iron Complexes. Eur J Org Chem 2008, 2008, 196. <http://dx.doi.org/10.1002/ejoc.200700919>
  • Roe Caroline, Sandoe Elizabeth J., Stephenson G. Richard, Anson Christopher E.: Stereoselectivity in the organoiron-mediated synthesis of (±)-mesembrine. Tetrahetron Lett 2008, 49, 650. <http://dx.doi.org/10.1016/j.tetlet.2007.11.137>
  • Knölker Hans-Joachim, R Reddy Kethiri, Fröhner Wolfgang: Transition Metals in Organic Synthesis, Part 84. Application of Iron- and Nickel-Mediated Coupling Reactions to the Total Synthesis of the Neuronal Cell Protecting Substance (±)-Carquinostatin A. HETEROCYCLES 2007, 74, 895. <http://dx.doi.org/10.3987/COM-07-S(W)84>
  • Zhao Jian, Larock Richard C.: Synthesis of Substituted Carbazoles by a Vinylic to Aryl Palladium Migration Involving Domino C−H Activation Processes. Org Lett 2005, 7, 701. <http://dx.doi.org/10.1021/ol0474655>
  • Knölker Hans-Joachim, Hopfmann Thomas: Transition metal complexes in organic synthesis. Part 65: Iron-mediated synthesis of carazostatin, a free radical scavenger from Streptomyces chromofuscus, and O-methylcarazostatin. Tetrahedron 2002, 58, 8937. <http://dx.doi.org/10.1016/S0040-4020(02)01180-8>