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Projekt Druckansicht

GRK 1038:  Katalysatoren und katalytische Reaktionen für die organische Synthese

Fachliche Zuordnung Molekülchemie
Förderung Förderung von 2005 bis 2013
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 374870
 
Erstellungsjahr 2015

Zusammenfassung der Projektergebnisse

Chemistry in general and Organic Synthesis in particular is an enabling science, which is in many cases the basis for innovation and development in the chemical and pharmaceutical industry and beyond. The development of an environmentally benign, energy saving, sustainable and cost efficient new quality of organic synthesis is more acute than ever. Catalysis in organic synthesis can be an ideal solution to these problems. Hence, the development of ever more efficient and selective catalysts and catalytic reactions for important synthetic transformations in organic synthesis is at the forefront of molecular sciences, and has been the central research topic of this international research training group. Under the roof of the international research training group “Catalysts and Catalytic Reactions for Organic Synthesis” (IRTG 1038) six research groups from the Faculty of Chemistry and Pharmacy of the University of Freiburg and five research groups from the Department of Chemistry at the University of Basel have combined their research and teaching activities in this innovative field of research. During two funding periods this IRTG has made significant contributions to the field with a total of nearly 800 original publications (437 FR/348 Bs) from the participating key researchers involved during the two funding periods. A total of 127 PhD students (81 FR/ 46 Bs) finished their scientific education. The excellent scientific training environment of this IRTG helped these PhD students to find rapidly excellent positions in both industry and academia.

Projektbezogene Publikationen (Auswahl)

  • Catalytic Desymmetrizing Intramolecular Heck Reaction: Evidence of an Unusual Hydroxy- Directed Migratory Insertion. Angew. Chem. 2005, 117, 152-155; Angew. Chem. Int. Ed. 2005, 44, 149-152
    M. Oestreich, F. Sempere-Culler, A.B. Machotta
  • Eine neue Synthese von Z-Pulvinonen : erste Arbeiten zu einer Totalsynthese von Kodaistatin und zur Ermittlung von dessen 3D-Struktur. Freiburg
    Kaczybura, Natasza
  • Kinetic Resolution of Chiral Secondary Alcohols by Dehydrogenative Coupling with Recyclable Silicon-Stereogenic Silanes. Angew. Chem. 2005, 117, 7793−7797; Angew. Chem. Int. Ed. 2005, 44, 7620−7624
    S. Rendler, G. Auer, M. Oestreich
  • OMCOS 13 (Conference report). Nachr. Chem. 2005, 53, 1069
    A.B. Machotta, M. Oestreich
  • Practical Synthesis of Allylic Silanes from Allylic Esters and Carbamates by Stereoselective Copper-Catalyzed Allylic Substitution Reactions. Adv. Synth. Catal. 2005, 347, 637−640
    M. Oestreich, G. Auer
  • An Enantioselective Access to an Anthracycline AB Synthon by a Desymmetrizing Heck Cyclization. Synlett 2006, 2965-2968
    M. Oestreich, F. Sempere-Culler, A.B. Machotta
  • Copper-Free and Copper-Promoted Conjugate Addition Reactions of Bis(triorganosilyl) Zincates. Synthesis 2006, 2113−2116
    G. Auer, B. Weiner, M. Oestreich
  • Organic Chemistry Online...and for Free? (Website review). Angew. Chem. 2006, 118, 7272; Angew. Chem. Int. Ed. 2006, 45, 7114
    A.B. Machotta, M. Oestreich
  • Preparation of a Privileged Silicon-Stereogenic Silane: Classical versus Kinetic Resolution. Adv. Synth. Catal. 2006, 348, 1171−1182
    S. Rendler, G. Auer, M. Keller, M. Oestreich
  • Reduktive Metallierung von Silylchloriden: Darstellung von siliciumstereogenen Silylanionen und Ausgangspunkt für übergangsmetallkatalysie Silyltransferreaktionen. Freiburg
    Auer, Gertrud
  • Rhodium-Catalyzed Enantioselective Conjugate Silyl Transfer: 1,4-Addition of Silyl Boronic Esters to cyclic Enones and Lactones. Angew. Chem. 2006, 118, 5803−5805; Angew. Chem. Int. Ed, 2006, 45, 5675−5677
    C. Walter, G. Auer, M. Oestreich
  • Silylzincation of Carbon−Carbon Multiple Bonds Revisited. Chem. Commun. 2006, 311−313
    G. Auer, M.Oestreich
  • Beiträge zu palladium(0)- und palladium(II)-katalysierten Heck-artigen C–C-Bindungsknüpfungen. Münster
    Machotta, Axel
  • Directed Branched-Regioselective Hydroformylation of 2-Substituted Allylic o-DPPB Esters. Eur. J. Org. Chem. 2007, 2497-2503
    B. Breit, C. Grünanger, O. Abillard
  • Ortho-Diphenylphosphanylbenzoyl-dirigierte Hydroformylierung als Schlüsselschritt einer iterativen Polypropionatsynthese. Freiburg
    Gebert, Antje
  • Oxygen Donor-Mediated Equilibration of Diastereomeric Alkene–Palladium(II) Intermediates in Enantioselective Desymmetrizing Heck Cyclizations. J. Am. Chem. Soc. 2007, 129, 13455-13463
    A.B. Machotta, B. F. Straub, M. Oestreich
  • Self-Assembled Bidentate Ligands for Ruthenium-Catalyzed Hydration of Nitriles. Organometallics 2007, 26, 2461-2464
    T. Šmejkal, B. Breit
  • Self-Assembly of Bidentate Ligands for Combinatorial Homogeneous Catalysis: Methanol- Stable Platforms Analogous to the Adenine Thymine Base Pair. Angew. Chem. 2007, 119, 3097-3099; Angew. Chem. Int. Ed. 2007, 46, 3037-3039
    C. Waloch, J. Wieland, M. Keller, B. Breit
  • Synthese von (R)-5,6-Dimethoxytryptophan und Arbeiten zur Totalsynthese der Indolalkaloide Geissochizin, Quaternin und Strictamin. Freiburg
    Kirchhoffer, Franz
  • Tandem Claisen Condensations / Transesterifications Between Arylacetate Enolates and Arylmethylene-Substituted 2,2-Dimethyl-1,3-dioxolan-4-ones: An Improved Synthesis of Z-Configured Pulvinones. Synthesis 2007, 118-130
    N. Kaczybura, R. Brückner
  • A Catalytic Asymmetric Fujiwara-Moritani Cyclization. Synlett 2008, 2271-2274
    J.A. Schiffner, A.B. Machotta, M. Oestreich
  • A Convenient Allylic Functionalization of Bis(prop-2-enyl)methanol by Direct Trimetalation. Synthesis 2008, 3692-3696
    A. Bigot, B. Breit
  • A Supramolecular Catalyst for Regioselective Hydroformylation of Unsaturated Carboxylic Acids. Angew. Chem. 2008, 120, 317-321; Angew. Chem. Int. Ed. 2008, 47, 311- 315
    T. Šmejkal, B. Breit
  • A Supramolecular Catalyst for the Decarboxylative Hydroformylation of a,b-Unsaturated Carboxylic Acids. Angew. Chem. 2008, 120, 4010-4013; Angew. Chem. Int. Ed. 2008, 47, 3946-3949
    T. Šmejkal, B. Breit
  • Allylation of N-Heterocycles with Allylic Alcohols Employing Self-Assembling Palladium Phosphane Catalysts. Org. Lett. 2008, 10, 1207-1210
    I. Usui, S. Schmidt, M. Keller, B. Breit
  • Asymmetric Synthesis – The Essentials (Second, Completely Revised Edition). Edited by Mathias Christmann and Stefan Bräse. Wiley-VCH, Weinheim 2008 (Book review). Synthesis 2008, 1163
    A.B. Machotta, M. Oestreich
  • Branched-Regioselective Hydroformylation with Catalytic Amounts of a Reversibly Bound Directing Group. Angew. Chem. 2008, 120, 7456-7459; Angew. Chem. Int. Ed. 2008, 47, 7346-7349
    C. U. Grünanger, B. Breit
  • Diastereoselective synthesis of α-tocopherol. Basel
    Buss, Axel
  • Enantioselective Synthesis of 2,6-Dideoxy Carbarsugars based on a Desymmetrizing Hydroformylation/Carbonyl Ene Cyclization Process. Chem. Commun. 2008, 6498-6500
    B. Breit, A. Bigot
  • Mimikry von Polyketid Synthasen mit Organokatalysatoren: Rationales Design und Kombinatorisches Screening. Basel
    Lubkoll, Jana
  • Molecular recognition in homogeneous transition metal catalysis : a biomimetic strategy for high selectivity. Freiburg
    Smejkal, Tomas
  • One pot desymmetrizing hydroformylation carbonyl ene cyclization application to the synthesis of carbohydrate mimetics. Freiburg
    Bigot, Aurélien
  • One-Pot Desymmetrizing Hydroformylation/Carbonyl Ene Cyclization Process: Straightforward Access to Highyl Functionalized Cyclohexanols. Org. Lett. 2008, 10, 5321-5324
    A. Bigot, D. Breuninger, B. Breit
  • Practical Synthesis of (E)-α,β-Unsaturated Carboxylic Acids Using a One-Pot Hydroformylation/Decarboxylative Knoevenagel Reaction Sequence. Adv. Synth. Cat. 2008, 350, 989-994
    S. T. Kemme, T. Šmejkal, B. Breit
  • Stereokomplementäre Herstellung 1,omega-distannylierter-Polyenbausteine und deren Anwendung in der jeweils ersten stereoselektiven Totalsynthese der Naturstoffe Cicutoxin und Pyrrhoxanthin. Freiburg
    Burghart, Jochen
  • Total Synthesis of Naturally Configured Pyrrhoxanthin, a Carotenoid Butenolide from Plankton. Angew. Chem. 2008, 120, 7777-7782; Angew. Chem. Int. Ed. 2008, 47, 7664-7668
    J. Burghart, R. Brückner
  • Totalsynthese von natürlich konfiguriertem Pyrrhoxanthin, einem Carotinoid-Butenolid aus Plankton. Total Synthesis of Naturally Configured Pyrrhoxanthin, a Carotenoid Butenolide from Plankton. Angew. Chem. 2008, 120, 7777-7782; Angew. Chem. Int. Ed. 2008, 47, 7664-7668
    J. Burghart, R. Brückner
  • A new assay format for NF-kb based on a triple helix and a fluorescence resonance energy transfer. Org. Biomol. Chem. 2009, 7, 3934-3939; Title page
    D. Altevogt, A. Hrenn, C. Kern, L. Clima, W. Bannwarth, I. Merfort
  • All Carbon Quaternary Centers via Ruthenium Catalyzed Hydroxymethylation of 2-Substituted Butadiene Mediated by Formaldehyde: Beyond Hydroformylation. J. Am. Chem. Soc. 2009, 131, 10366-10367
    T. Smejkal, H. Han, B. Breit, M. Krische
  • Asymmetric synthesis of 2,2-disubstituted chromanols. Basel
    Chapelat, Julien
  • Chromatography-free enzymatic kinetic resolution of secondary alcohols. Basel
    Maywald, Matthias
  • Cu[Al(OR^F)4] Starting Materials and their Application in the Preparation of [Cu(Sn)]+ (n = 12, 8) Complexes. Chem. Eur. J. 2009, 15, 6663-6677
    Gustavo Santiso-Quinones, Alexander Higelin, Julia Schäfer, Robin Brückner, Carsten Knapp, Ingo Krossing
  • Dual Palladium- and Proline-Catalyzed Allylic Alkylation of Enolizable Ketones and Aldehydes with Allylic Alcohols. Org. Lett. 2009, 11, 1453-1456
    I. Usui, S. Schmidt, B. Breit
  • Entwicklung eines iterativen Syntheseweges für Polyketidstrukturen sowie Untersuchungen zur Synthese und Biosynthese von Gabaculin. Freiburg
    Rieder, Oliver
  • Feasibility study for a new assay for NF-kappaB and DNA-supported catalysis. Freiburg
    Altevogt, Dominik
  • High-Yielding Large-Scale Syntheses of Enantiomerically Pure NOBIN and a NOBIN-Based Enantiomerically Pure NHC Precursor. Synlett 2009, 109-111
    D. Sälinger, R. Brückner
  • Intramolecular Mizoroki-Heck Reactions – Formation of Carbocycles. In The Mizoroki-Heck Reaction (Ed.: M. Oestreich), Wiley, Chichester, 2009, Chapter 5
    A.B. Machotta, M. Oestreich
  • Iridium-katalysierte Hydrierung unfunktionalisierter Olefine. Basel
    Schrems, Marcus
  • Iterative Synthesis of (Oligo)deoxypropionates via Zinc-Catalyzed Enantiospecific sp −sp Cross-Coupling. Org. Lett. 2009, 11, 4668-4670
    G. J. Brand, C. Studte, B. Breit
  • Konformationsdesign und stereoselektive Synthese von Trichostatin A-Analoga als Inhibitoren von Histondesacetylasen : Synthese von Nicotinmidadenindinucleotid-Derivaten. Freiburg
    Brand, Gabriel
  • P-Chiral phosphorus ligands: Synthesis and application in asymmetric hydrogenation. Basel
    Gschwend, Björn
  • Peptides as catalysts for asymmetric 1,4-addition reactions of aldehydes to nitroolefins. Basel
    Wiesner, Markus
  • Selectivity Enhancement for the Jacobsen-Katsuki Epoxidation in Fluorinated Solvents. Helv. Chim. Acta 2009, 91, 623-628
    Nizam Havare, Dietmar A. Plattner
  • Supramolecular Catalyst for Aldehyde Hydrogenation and Tandem Hydroformylation-Hydrogenation. Angew. Chem. 2009, 121, 8166-8170; Angew. Chem. Int. Ed. 2009, 48, 8022-8026
    L. Diab, T. Smejkal, B. Breit
  • Synthesen prochiraler Alkohole mit enantiotopen Bromalkenyl- oder Bromarylsubstituenten : Desymmetrisierung von Bis(bromaryl)alkoholen durch ersten asymetrischen Halogen/Metall-Austausch. Freiburg
    Sälinger, Daniel
  • A combinatorial approach to the identification of self-assembled ligands for rhodium-catalyzed asymmetric hydrogenation. Nature Chemistry 2010, 2, 832-837
    J. Wieland, B. Breit
  • Chiral pyridyl phosphinite catalysts and the development of structure selectivity relationships in the asymmetric hydrogenation of trisubstituted alkenes. Basel
    Woodmansee, David
  • Combinatorial organocatalyst development and screening of conjugate additions. Basel
    Fleischer, Ivana
  • Combined Transition-Metal- and Organocatalysis: An Atom Economic C3 Homologation of Alkenes to Carbonyl and Carboxylic Compounds. Chem. Eur. J. 2010, 16, 3423-3433
    S. T. Kemme, T. Smejkal, B. Breit
  • Conversion of Conjugated Enones into Enantiomerically Pure β-Hydroxyketones or 1,3-Diols. Samarium(II)-Bromide Reductions of Protected α,β-Dihydroxyketones. Eur. J. Org. Chem. 2010, 4785-4801
    A. Zörb, R. Brückner
  • Dual transition metal- and organo-catalyst catalyzed C-C bond formation. Freiburg
    Usui, Ippei
  • Economic Large-Scale Synthesis of o- and m-Diphenylphosphinobenzoic Acids. Synthesis 2010, 1924-1928
    S. T. Kemme, Y. Schmidt, C. U. Grünanger, A. C. Laungani, C. Herber, B. Breit
  • Enantioselective Total Synthesis of the Unnatural and the Natural Stereoisomers of Vittatalactone. J. Org. Chem. 2010, 75, 4424-4433
    Y. Schmidt, K. Lehr, U. Breuninger, G. Brand, T. Reiss, B. Breit
  • Entwicklung einer kovalent aber reversibel gebundenen Katalysator-dirigierenden Gruppe für regio- und diastereoselektive Hydroformylierungen. Freiburg
    Grünanger, Christian
  • Exceptionally Active Catalysts for the Formation of Carbamates from Alcohols and Isocyanates: Molybdenum(VI) Dichloride Dioxide and its DMF Complex. Synlett 2010, 2429-2434
    C. Stock, R. Brückner
  • Multifunktionelle, fluoreszente PerfluorPEG-Linker : Synthese, Charakterisierung und Applikation in Einzelenzymspektroskopie, in Fluor-Fluor-Interaktionsquantifizierung und in weiteren Anwendungen. Freiburg
    Rapp, Hartmut
  • Remote Control of Regio- and Diastereoselectivity in the Hydroformylation of Bishomoallylic Alcohols with Catalytic Amounts of a Reversibly Bound Directing Group. Angew. Chem. 2010, 122, 979-982; Angew. Chem. Int. Ed. 2010, 49, 967-970
    C. U. Grünanger, B. Breit
  • Samarium(II)-halogenid-vermittelte Alpha-Defunktionalisierung geschützter Alpha,Beta-Dihydroxycarbonylverbindungen und deren Anwendung in Synthese von Statinseitenketten : 1,3-Diolsynthesen. Freiburg
    Zörb, Andreas
  • Samarium(II)-halogenid-vermittelte Alpha-Defunktionalisierung geschützter Alpha,Beta-Dihydroxycarbonylverbindungen und deren Anwendung in Synthese von Statinseitenketten: 1,3-Diolsynthesen. Freiburg
    Zörb, Andreas
  • Supramolekulare Phosphanliganden auf Basis der Adenin/Thymin- und Cytosin/Guanin- DNA-Basenpaarung: Selbstassoziierende Liganden für die homogene Katalyse. Freiburg
    Wieland, Jörg
  • The Reaction of White Phosphorus with NO+/NO2+[Al(OR^F)4]-: The [P4NO]+ Cluster Formed by an Unexpected Nitrosonium Insertion. Angew. Chem., Int. Ed. Engl. 2010, 49, 8139-8143
    Tobias Köchner, Sebastian Riedel, Anna J. Lehner, Harald Scherer, Ines Raabe, Tobias A. Engesser, Franziska W. Scholz, Urs Gellrich, Philipp Eiden, Roberto A. Paz Schmidt, Dietmar A. Plattner, Ingo Krossing
  • The Reaction of White Phosphorus with NO+/NO2+[Al(ORF)4]−: The [P4NO]+ Cluster Formed by an Unexpected Nitrosonium Insertion. Angew. Chem. 2010, 122, 8316–8320; Angew. Chem. Int. Ed. 2010, 49, 8138-8143
    Tobias Köchner, Sebastian Riedel, Anna J. Lehner, Harald Scherer, Ines Raabe, Tobias A. Engesser, Franziska W. Scholz, Urs Gellrich, Philipp Eiden, Roberto A. Paz-Schmidt, Dietmar A. Plattner, Ingo Krossing
  • Transition-State Stabilization by a Secondary Substrate-Ligand Interaction: A New Design Principle For Highly Efficient Transition-Metal Catalysis. Chem. Eur. J. 2010, 16, 2470-2478
    T. Smejkal, D. Gribkov, J. Geier, M. Keller, B. Breit
  • A Serendipitous Synthesis of (+)-Gregatin B. Second Structure Revision of the Aspertetronins, Gregatins, and Graminin A. Structure Revision of the Penicilliols. Org. Lett. 2011, 13, 2730-2733
    H. Burghart-Stoll, R. Brückner
  • Asymmetric Dihydroxylations of 1-Substituted (E)- and (Z)-3-Methylpent-2-en-4-ynes: Full Compliance with the Sharpless Mnemonic Re-established and Embellished. Org. Lett. 2011, 13, 1020-1023
    H. Burghart-Stoll, O Böhnke, R. Brückner
  • Asymmetric Dihydroxylations of Enynes with a Trisubstituted C=C Bond. An Unprecedented Route to γ-Lactone Building Blocks with a Quaternary Stereocenter. Org. Lett. 2011, 13, 1016-1019
    H. Burghart-Stoll, T. Kapferer, R. Brückner
  • Chemistry in ionic liquids and prediction of their transport properties. Freiburg
    Eiden, Philipp
  • Chirale mono- und bidentate Phosphorliganden für die enantioselektive Metall-katalysierte Hydrierung. Basel
    Frank, Dominik
  • Diastereoselective Hydroformylation of 2,5-Cyclohexadienyl-1-carbinols with Catalytic Amounts of a Reversibly Bound Directing Group. Org. Lett. 2011, 13, 612-615
    I. Usui, K. Nomura, B. Breit
  • Entwicklung neuer P,N-Liganden und ihre Anwendungen in der Iridium-katalysierten Hydrierung von α,β-ungesättigten Carbonsäureestern. Basel
    Tröndlin, Lars
  • Formation of Quaternary Carbon Centers by Highly Regioselective Hydroformylation with Catalytic Amounts of a Reversibly 39Bound Directing Group. Chem Eur. J. 2011, 17, 8555-8558
    Y. Ueki, H. Ito, I. Usui, B. Breit
  • Iron Nanoparticles Supported on Chemically-Derived Graphene: Catalytic Hydrogenation with Magnetic Catalyst Separation. Adv. Synth. Cat. 2011, 353, 523-527
    M. Stein, J. Wieland, P. Steurer, F. Tölle, R. Mülhaupt, B. Breit
  • On the Origin of Ligand Self-Assembling Through Complementary Hydrogen-Bonding in the Coordination Sphere of a Transition Metal Center: The 6-Diphenylphosphanylpyridin-2(1H)-one system J. Am. Chem. Soc., 133, 964 (2011)
    U. Gellrich, W. Seiche, M. Keller, B. Breit, J. Huang and M. Meuwly
  • Sn/Li Exchange Reactions in 1,w-Distannylated Conjugated Trienes and Tetraenes: An Enabling Step for Polyene Synthesis. Eur. J. Org. Chem. 2011, 150-165
    J. Burghart, R. Brückner
  • Stereocomplementary Syntheses of 1,ω-Distannylated E,Z-Isomeric Conjugated Trienes, Tetraenes, and Pentaenes. Chem. Eur. J. 2011, 17, 6469-6483
    J. Burghart, A. Sorg, R. Brückner
  • Stereoselective Reduction of 2-Hydroxy Ketones towards syn- and anti-1,2-Diols. Adv. Synth. Catal. 2011, 353, 2359–2362
    Syed Masood Husain, Thomas Stillger, Pascal Dünkelmann, Melanie Lödige, Lydia Walter, Elke Breitling, Martina Pohl, Mara Bürchner, Ingo Krossing, Michael Müller, Diego Romano, Francesco Molinari
  • Stereoselective Reduction of 2-Hydroxy Ketones towards syn- and anti-1,2-Diols. Advanced Synthesis & Catalysis 2011, 353, 2359-2362
    S. M. Husain, T. Stillger, P. Dunkelmann, M. Lodige, L. Walter, E. Breitling, M. Pohl, M. Bürchner, I. Krossing, M. Müller, D. Romano, F. Molinar
  • Strukturrevidierende Synthese von Gregatin B : Entwicklung eines variati-onsfähigen Zugangs zu den revidierten Strukturen der Aspertetronine Gregatine. Freiburg
    Burghart-Stoll, Heike
  • Studien zur Totalsynthese von TMC-151 : Untersuchungen zur vinylogen Mukaiyama Aldolreaktion nach Kobayashi. Freiburg
    Breuninger, Ulrich
  • [P9]+[Al(ORF)4]-, the Salt of a Homopolyatomic Phosphorus Cation. Angew. Chem. 2012, 124, 6635–6637; Angew. Chem. Int. Ed. 2012, 51, 6529-6531
    Tobias Köchner, Tobias A. Engesser, Harald Scherer, Dietmar A. Plattner, Alberto Steffani, Ingo Krossing
  • A Se19 Homocycle Complexed by Two Copper(I) Ions. Angew. Chem. 2012, 124, 6112–6115; Angew. Chem. Int. Ed. 2012, 51, 6009-6012
    ulia Schaefer, Alberto Steffani, Dietmar A. Plattner, Ingo Krossing
  • Attachment of Proteins to Surfaces by Fluorous-Fluorous Interactions Restoring Their Structure and Activity. ChemPlusChem 2012, 77, 1066- 1070
    H. M. Rapp, S. Bacher, A. Ahrens, W. Rapp, B. Kammerer, G. U. Nienhaus, W. Bannwarth
    (Siehe online unter https://doi.org/10.1002/cplu.201200234)
  • Biomimetic asymmetric synthesis of (R)-GTRI-02 and (3S,4R)-3,4-dihydroxy-3,4-dihydronaphthalen-1(2H)-ones. Org. Lett. 2012, 14, 3600–3603
    Syed Masood Husain, Michael A. Schätzle, Caroline Röhr, Steffen Lüdeke, Michael Müller
    (Siehe online unter https://doi.org/10.1021/ol301305p)
  • Chiral proline-based ligands for iridium-catalyzed asymmetric hydrogenation. Basel
    Rageot, Denise
  • Development and evaluation of chiral catalysts for asymmetric C-C and C-H bond forming reactions. Basel
    Ebner, Christian
  • Development of a bidentate lewis acid catalyzed inverse electron demand diels-alder reaction of 1,2-diazines for the synthesis of substituted arenes. Basel
    Kessler, Simon
  • Drei für Zwei, die Entwicklung dreier Schlüsselmethoden für zwei neuartige Totalsynthesen der Polyol-Polyen-Makrolide Amphotericin B und RK-397: desymmetrisierende asymmetrische Dihydroxylierungen prochiraler 1,7-disubstituierter Diallyldarbinole; MoO2Cl2(DMF)2-katalysierte Additionen von Akoholen an Isocyanate; Phenylselanol-vermittelte Desoxygenierungen in alpha-Position zu Akzeptoren. Freiburg
    Stock, Christian
  • Enantioselektive Epoxidierung mit Metall(salen)-Komplexen - Oxidative Spaltung und Umlagerung organischer Verbindungen. Freiburg
    Havare, Nizam
  • Enzymatic reduction of anthrahydoquinones: implications für chrysophanol, monodictyphenone and related xanthone biosyntheses. J. Am. Chem. Soc. 2012, 134, 14742–14745
    Michael A. Schätzle, Syed Masood Husain, Sascha Ferlaino, Michael Müller
  • Fluor-Fluor-Wechselwirkungen zur nicht-kovalenten Immobilisierung : Synthese und Immobilisierung von Katalysatoren an Perfluoriertem Kieselgel und in amphiphilen Systemen, sowie deren Anwendung in Diels-Alder Reaktionen und Ringschluss-Metathesen. Freiburg
    Hensle, Eva
  • Human Carbonic Anhydrase II: a Novel Scaffold for Artificial Metallo-enzymes. Basel
    Monnard, Fabien
  • Hydrogen-Bond and Solvent Dynamics in Transition Metal Complexes: A Combined Simulation and NMR- Investigation J. Phys. Chem. B, 116, 14406 (2012)
    J. Huang, D. Häussinger, U. Gellrich, W. Seiche, B. Breit and M. Meuwly
    (Siehe online unter https://doi.org/10.1021/jp309412r)
  • Metabolische Divergenz durch NADPH-abhängige Reduktion von Ketotautomeren phenolischer Verbindungen. Freiburg
    Schätzle, Michael
  • Mild and High-Yielding Molybdenum(VI) Dichloride Dioxide Catalyzed Formation of Mono- and Oligocarbamates from Alcohols and Aromatic or Aliphatic Isocyanates. Adv. Synth. Catal. 2012, 354, 2309-2330
    C. Stock, R. Brückner
  • Oxidative Cleavage and Rearrangement of Aryl Epoxides Using Iodosylbenzene: on Criegee’s Trail. Helv. Chim. Acta 2012, 95, 2036-2042
    Nizam Havare, Dietmar A. Plattner
  • Oxidative Cleavage of α-Arylaldehydes Using Iodosylbenzene. Org. Lett. 2012, 14, 5078-5081
    Nizam Havare, Dietmar A. Plattner
  • Synthesis and Application of Strong Bronsted Acids Generated from the Lewis Acid Al(OR^F)3 and an Alcohol. Organometallics 2012, 31, 7485-7491
    A. Kraft, J. Beck, G. Steinfeld, H. Scherer, D. Himmel and I. Krossing
    (Siehe online unter https://doi.org/10.1021/om300776a)
  • Synthesis and Oxidation of Hexafluoroisopropoxyborylferrocenes. Pure and Applied Chemistry 2012, 84, 2317-2324
    Hannes Böhrer, Nils Trapp, Harald Scherer, and Ingo Krossing
    (Siehe online unter https://doi.org/10.1351/PAC-CON-12-02-14)
  • Synthesis, Characterization, and Application of Two Al(OR^F)3 Lewis Superacids.Chem. Eur. J. 2012, 18, 9371-9380
    Anne Kraft, Nils Trapp, Daniel Himmel, Hannes Böhrer, Peter Schlüter, Harald Scherer, and Ingo Krossing
    (Siehe online unter https://doi.org/10.1002/chem.201200448)
  • Tandem Rhodium-Catalyzed Hydroformylation-Hydrogenation of Alkenes by Employing a Cooperative Ligand System. Angew. Chem. 2012, 124, 2220-2224; Angew. Chem. Int. Ed. 2012, 51, 2178-2182
    D. Fuchs, G. Rousseau, L. Diab, U. Gellrich, B. Breit
    (Siehe online unter https://doi.org/10.1002/anie.201108946)
  • Tetrahydroxynaphthalene Reductase – Catalytic Properties of an Enzyme Involved in Reductive Asymmetric Naphthol Dearomatization. Angew. Chem. 2012, 124, 2697–2700; Angew. Chem. Int. Ed. 2012, 51, 2643–2466
    Michael A. Schätzle, Stephan Flemming, Syed Masood Husain, Michael Richter, Stefan Günther, Michael Müller
    (Siehe online unter https://doi.org/10.1002/anie.201107695)
  • Total Syntheses of the Gregatins A-D and Aspertetronin A. Structure Revision of these Compounds and Aspertetronin B and Plausible Structure Revisions of Gregatin E, Cyclogregatin, Graminin A, the Penicilliols A and B, and the Huaspenones A and B. Eur. J. Org. Chem. 2012, 3978-4017
    H. Burghart-Stoll, R. Brückner
    (Siehe online unter https://doi.org/10.1002/ejoc.201200207)
  • Untersuchungen zur asymmetrischen, Iridium-katalysierten Hydrierung konjugierter Diene und Anwendungen in der Naturstoffsynthese. Basel
    Schumacher, Andreas
  • [Au(C2H4)3]+ [Al(OR^F)4]- a Stable Homoleptic Ethene-Gold Complex. Eur. J. Inorg. Chem. 2013, 2712-2717
    J. Schaefer, D. Himmel and I. Krossing
    (Siehe online unter https://doi.org/10.1002/ejic.201201538)
  • A Systematic Investigation of Coinage Metal Carbonyl Complexes Stabillized by Fluorinated Alkoxy Aluminates. Chem. Eur. J. 2013, 19, 12468-12485
    J. Schaefer, A. Kraft, S. Reininger, G. Santiso-Quinones, D. Himmel, N. Trapp, U. Gellrich, B. Breit, I. Krossing
  • Arbeiten zur Synthese der konstitutionell isomeren C1-C21-Polyolabschnitte der unnatürlichen Enantiomere von Amphotericin B, Nystatin A1, Ampcin A und 28,29-Didehydronystatin A1. Freiburg
    Kamptmann, Sonja
  • Atomistic Simulations of Transition Metal Catalyzed Reactions Using Specialized Force Fields and Quantum Mechanical Methods. Basel
    Hofmann, Franziska
  • Computational modelling of metal-mediated protein-ligand interactions. Basel
    Schmid, Maurus
  • Crystal Structure Determination of the Nonclassical 2-Norbornyl Cation. Science 2013, 341, 62-64
    F. Scholz, D. Himmel, F. W. Heinemann, P. v. R. Schleyer, K. Meyer,* I. Krossing
    (Siehe online unter https://doi.org/10.1126/science.1238849)
  • De Novo-Synthesen DNA-Basierter Hybridkatalysatoren und deren Anwendung in DIELS-ALDER-Reaktionen. Freiburg
    Barudio, Sandra
  • Entwicklung neuartiger Methoden für die Totalsynthese von Naturstoffen, Entwicklung des ersten asymmetrischen Sulfoxid-Magnesium Austausches, Einsatz von mIBG-Analoga in der Therapie des Neuroblastom Tumors. Freiburg
    Hampel, Thomas
  • Exploring the coodination chemistry of univalent Gallium and Indium. Freiburg
    Higelin, Alexander
  • First Crystal Structure of a Fungal High-redox Potential Dye-decolorizing Peroxidase: Substrate Interaction Sites and Long-range Electron Transfer. J. Biol. Chem. 2013, 288, 4095-4102
    Eric Strittmatter, Christiane Liehrs, René Ullrich, Sabrina Wachter, Martin Hofrichter, Dietmar A. Plattner, Klaus Piontek
    (Siehe online unter https://doi.org/10.1074/jbc.M112.400176)
  • Iridium-catalyzed asymmetric hydrogenation : develop-ment of New N,P ligands and hydrogenation of alkenylboronic esters. Basel
    Ganic, Adnan
  • Mono thiomalonates as thioester enolate equivalents - organo-catalytic stereoselective addition reactions to different electrophiles. Basel
    Clerici, Paolo
  • Neues über Deslongchamps-Anellierungen : Erweiterung der Substratpalette; Nachweis der Zweistufigkeit; Anwendung in Arbeiten zur Synthese der Dihydroagarofurane 3-Desoxymaytol und Euonyminol. Freiburg
    Petrovic, Denis
  • Peptide catalyzed conjugate addition reactions of aldehydes to nitroolefins. Basel
    Duschmalé, Jörg
  • Radical formation on a conserved tyrosine residue is crucial for DyP activity. Arch. Biochem. Biophys. 2013, 537, 161-167
    Eric Strittmatter, Sabrina Wachter, Christiane Liehrs, René Ullrich, Martin Hofrichter, Dietmar A. Plattner, Klaus Piontek
    (Siehe online unter https://doi.org/10.1016/j.abb.2013.07.007)
  • Realistic Energy Surfaces for Real World Systems: an IMOMO CCSD(T):DFT scheme for the Rhodium Catalyzed Hydro-formylation with the 6-DPPon ligand. Chem. Eur. J. 2013, 19, 16272-16281
    U. Gellrich, D. Himmel, M. Meuwly, B. Breit
    (Siehe online unter https://doi.org/10.1002/chem.201302132)
  • Realistic Energy Surfaces for Real World Systems: An IMOMO CCSD(T):DFT scheme for the Rhodium Catalyzed Hydroformylation with the 6-DPPon ligand Chem. Eur. J., 19, 16272-16281 (2013)
    U. Gellrich, D. Himmel, M. Meuwly, and B. Breit
    (Siehe online unter https://doi.org/10.1002/chem.201302132)
  • Room Temperatur Ambient Pressure (RTAP)-Hydroformylation in Water Using a Self-Assembling Ligand. Adv. Synth. Cat. 2013, 355, 2071-2075
    A. T. Straub, M. Otto, I. Usui, B. Breit
    (Siehe online unter https://doi.org/10.1002/adsc.201300258)
  • Stereoselective Mannich Reactions to Mono Thiomalonates & Screening for Peptidic Triazolium Salt Based Catalysts. Basel
    Bahlinger, Annette
  • Substrate-Dependent Stereospecificity of Tyl-KR1, an Isolated Polyketide Synthase Ketoreductase Domain from Streptomyces fradiae. Chem. Eur. J. 2013, 19, 8922–8928
    Matthias Häckh, Michael Müller, Steffen Lüdeke
    (Siehe online unter https://doi.org/10.1002/chem.201300554)
  • Superacidic or Not ...? Synthesis, Characterisation, and Acidity of the Room-Temperature Ionic Liquid [C(CH3)3]+ [Al2Br7]-. Chem. Eur. J. 2013, 19, 109-116
    F. Scholz, D. Himmel, H. Scherer and I. Krossing
    (Siehe online unter https://doi.org/10.1002/chem.201203260)
  • Synthesis of new phosphino-oxazoline ligands for asymmetric catalysis. Basel
    Padevet, Jaroslav
  • Synthetic and mechanistic investigations of iridium-catalysed imine hydrogenation. Basel
    Schramm, York
  • Systematic Investigation of Coinage Metal Carbonyl Complexes Stabilized by Fluorinated Alkoxy Aluminates. Chem. Eur. J. 2013, 19, 12468-12485
    Julia Schaefer, Anne Kraft, Stefanie Reininger, Gustavo Santiso-Quinones, Daniel Himmel, Nils Trapp, Urs Gellrich, Bernhard Breit, Ingo Krossing
    (Siehe online unter https://doi.org/10.1002/chem.201204544)
  • Tandem decarboxylative hydroformylation-hydrogenation reaction of α,β-unsaturated carboxylic acids toward aliphatic alcohols under mild conditions employing a supramolecular catalyst system. Chem. Commun. 2013, 49, 9737-9739
    L. Diab, U. Gellrich, B. Breit
  • Tandem Hydroformylation/Biginelli Reaction. Synlett 2013, 1657-1662
    D. Fuchs, M. Nasr-Esfahani, L. Diab, T. Smejkal, B. Breit
    (Siehe online unter https://doi.org/10.1055/s-0033-1339298)
  • Totalsynthese der Polyenoyltetramsäure-Antibiotika alpha- und beta-Lipomycin und Aufklärung der Stereostruktur von deren Seitenkette. Freiburg
    Hofferberth, Max
  • Univalent Gallium Salts of Weakly Coordinating Anions: Effective Initiators/Catalysts for the Synthesis of Highly Reactive Polyisobutylene. Organometallics 2013, 32, 6725–6735
    Martin R. Lichtenthaler, Alexander Higelin, Anne Kraft, Sarah Hughes, Alberto Steffani, Dietmar A. Plattner, John M. Slattery, Ingo Krossing
    (Siehe online unter https://doi.org/10.1021/om4005516)
  • "Verdreh-mein-nicht": 5,5-verbrückte Biphenyl-2,2 ́-diphosphane; eine neue Klasse an Liganden für die Asymmetrische Katalyse. Freiburg
    Sartorius, Frank
  • A Janus headed Lewis Superacid: Simple Access to, and first Application of Me3Si-F-Al(OR )3. Chem. Eur. J. 2014, 20, 1218-1222
    M. Rohde, L. O. Müller, D. Himmel, H. Scherer, I. Krossing
    (Siehe online unter https://doi.org/10.1002/chem.201303671)
  • Boron-based Lewis acids and anions: an experimental and theoretical study. Freiburg
    Böhrer, Hannes
  • Dative Bonds in Main-Group Compounds: A Case for Fewer Arrows! Angew. Chem. Int. Ed. Engl. 2014, 53, 370-374
    Daniel Himmel, Ingo Krossing, and Andreas Schnepf
    (Siehe online unter https://doi.org/10.1002/anie.201300461)
  • Dative or Not Dative? Angew. Chem. Int. Ed. 2014, 53, 6047-6048
    D. Himmel, I. Krossing, A. Schnepf
    (Siehe online unter https://dx.doi.org/10.1002/anie.201403078)
  • Dye-Decolorizing Peroxidase (DyP). Encyclopedia of Inorganic and Bioinorganic Chemistry, Scott, R.A., Ed., Wiley, 2014, pp. 1-13
    Erich Strittmatter, Dietmar A. Plattner, Klaus Piontek
  • Efficient Synthesis of New Fluorinated Building Blocks by means of Hydroformylation. Chimia 2014, 68, 371-377
    L. Fanfoni, L. Diab, T. Smejkal, B. Breit
    (Siehe online unter https://dx.doi.org/10.2533/chimia.2014.371)
  • Enzymkatalyse im Mikroreaktor : Immobilisierung von alpha-Chymotrypsin und Ribonuklease H mittels Fluor-Fluor-Wechselwirkungen. Freiburg
    Ahrens, Anika
  • Funktionelle und strukturelle Charakterisierung von 4-Hydroxyphenylpyruvat Dioxygenasen und 4-Hydroxymandelat Synthasen. Freiburg
    Frick, Eduard
  • Hydroformylation and Related Carbonylation Reactions of Alkenes, Alkynes, and Allenes. In: Gary A. Molander and Paul Knochel (eds.), Comprehensive Organic Synthesis, 2nd Edition, Vol 4, Oxford: Elsevier; 2014, pp. 995-1053
    B. Breit and L. Diab
  • Iridium-Catalyzed Asymmetric Hydrogenation of Furan Derivatives and Thiophene 1,1-Dioxides. Basel
    Pauli, Larissa
  • Mechanistic Investigations of the Rhodium Catalyzed Propargylic CH Activation. J. Am. Chem. Soc. 2014, 136, 1097-1104
    U. Gellrich, A. Meißner, A. Steffani, M. Kähny, H.-J. Drexler, D. Heller, D. A. Plattner, B. Breit
    (Siehe online unter https://doi.org/10.1021/ja411204d)
  • Mechanistic Investigations of the Rhodium Catalyzed Propargylic CH Activation. J. Am. Chem. Soc. 2014, 136, 1097-1104
    Urs Gellrich, Antje Meissner, Alberto Steffani, Matthias Kähny, Hans-Joachim Drexler, Detlef Heller, Dietmar A. Plattner, Bernhard Breit
    (Siehe online unter https://doi.org/10.1021/ja411204d)
  • Modulation der Reaktivitäten von Diels-Alder-Reaktionen durch Komplexierung von chelatisierenden Liganden und Modifizierung von Tetrazinderivaten. Freiburg
    Sterk, Markus
  • Modulation of Olefin Metathesis Reactions by Chelation. Eur. J. Org. Chem. 2014, 24, 5331-5345
    S. Scherbakow, M. Keller, W. Bannwarth
    (Siehe online unter https://doi.org/10.1002/ejoc.201402319)
  • Modulierung von Olefinmetathese-Reaktionen durch neue chelatisierende Hoveyda-Grubbs-artige Katalysatoren. Freiburg
    Scherbakow, Swetlana
  • Phenol oxidation by DyP-type peroxidases in comparison to fungal and plant peroxidases. J. Mol. Cat. B 2014, 103, 41-46
    Christiane Liehrs, Elizabet Aranda, Eric Strittmatter, Klaus Piontek, Dietmar A. Plattner, Holger Zorn, René Ullrich, Martin Hofrichter
    (Siehe online unter https://doi.org/10.1016/j.molcatb.2013.09.025)
  • Straightforward Synthesis of the Brønsted Acid hfipOSO3H and its Application for the Synthesis of Protic Ionic Liquids. Angew. Chem. Int. Ed. 2014, 53, 6637-6640
    W. Beichel, Panzer, Johann M. U., J. Hätty, X. Ye, D. Himmel, I. Krossing
    (Siehe online unter https://doi.org/10.1002/anie.201402577)
  • The Superacidic System HBr-AlBr3: Protonation of Benzene and Ordered Crystal Structure of [C6H7]+[Al2Br7]-. Angew. Chem. Int. Ed. Engl. 2014, 53, 1689- 1692
    Franziska Scholz, Daniel Himmel, Lea Eisele, Wiebke Unkrig and Ingo Krossing
    (Siehe online unter https://doi.org/10.1002/anie.201308120)
  • Unprecedented role of hydronaphthoquinone tautomers in biosynthesis. Angew. Chem. 2014, 126, 9964–9969; Angew. Chem. Int. Ed. 2014, 53, 9806–9811
    Syed Masood Husain, Michael A. Schätzle, Steffen Lüdeke, Michael Müller
    (Siehe online unter https://doi.org/10.1002/ange.201404560)
  • Untersuchungen zur Stereoselektivität und -spezifität der Ketoreduktase Tyl-KR1 aus Streptomyces fradiae. Freiburg
    Häckh, Matthias
  • α- und β-Lipomycin:Totalsynthesen auf der Grundlage sequentieller Stille-Kupplungen und Zuordnung der absoluten Konfiguration aller stereogenen Zentren. α- and β-Lipomycin: Total Syntheses by Sequential Stille Couplings and Assignment of the Abolsute Configuration of all Stereogenic Centers. Angew. Chem. 2014, 126, 7456-7462; Angew. Chem. Int. Ed. 2014, 53, 7328-7334
    M. L. Hofferberth, R. Brückner
    (Siehe online unter https://doi.org/10.1002/anie.201402255)
  • σ- or π-Coordination? Complexes of Univalent Gallium Salts with Aromatic Nitrogen Bases. Eur. J. Inorg. Chem. 2014, 26, 4335-4341
    M. R. Lichtenthaler, F. Stahl, D. Kratzert, B. Benkmil, H. A. Wegner, I. Krossing
    (Siehe online unter https://doi.org/10.1002/ejic.201402360)
  • Dihydrogen Activation at Non-Metallic Centers. Basel
    Auth, Johanna
    (Siehe online unter https://dx.doi.org/10.5451/unibas-006387324)
  • Modulation of Reactivities of Dienophiles for Diels-Alder Reactions via Complexation of alpha/beta-Unsaturated Chelating Amides. Helv. Chim. Acta 2015, 98, 287-307
    M. Sterk, W. Bannwarth
  • Oxidation and nitration of mononitrophenols by a DyP-type peroxidase. Arch. Biochem. Biophys. 2015, 574, 86-92
    Enrico Bütter, René Ullrich, Eric Strittmatter, Klaus Piontek, Dietmar A. Plattner, Martin Hofrichter, Christiane Liers
    (Siehe online unter https://doi.org/10.1016/j.abb.2015.03.003)
  • The toolbox of Auricularia auricula-judae dye-decolorizing peroxidase – Identification of three new potential substrate-interaction sites. Arch. Biochem. Biophys. 2015, 574, 75-85
    Eric Strittmatter, Kerstin Serrer, Christiane Liehrs, René Ullrich, Martin Hofrichter, Klaus Piontek, Erich Schleicher, Dietmar A. Plattner
    (Siehe online unter https://doi.org/10.1016/j.abb.2014.12.016)
 
 

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