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Paul Knochel

Researcher Next ID · RN-032023

Researcher · Chemistry

Ludwig-Maximilians-Universität München

Munich, Germany

Accepting doctoral researchersFunding unknown
Works count
2,968
Citation count
58,663
H-index
110
i10-index
783

Research interests

Chemistry
Coordination Chemistry and Organometallics
Asymmetric Synthesis and Catalysis
Catalytic Cross-Coupling Reactions
Catalytic C–H Functionalization Methods
Asymmetric Hydrogenation and Catalysis

Publications

  • Oriented Films of Conjugated 2D Covalent Organic Frameworks as Photocathodes for Water Splitting

    Journal of the American Chemical Society · 2017 · 10.1021/jacs.7b06081

  • Synthesis of Bicyclo[1.1.1]pentane Bioisosteres of Internal Alkynes and para ‐Disubstituted Benzenes from [1.1.1]Propellane

    Angewandte Chemie International Edition · 2017 · 10.1002/anie.201706799

  • Recent Developments in Negishi Cross-Coupling Reactions

    ACS Catalysis · 2016 · 10.1021/acscatal.5b02718

  • Room Temperature Synthesis of Covalent–Organic Framework Films through Vapor-Assisted Conversion

    Journal of the American Chemical Society · 2014 · 10.1021/ja510895m

  • Comprehensive organic synthesis

    Elsevier eBooks · 2014

  • Isoreticular Two-Dimensional Covalent Organic Frameworks Synthesized by On-Surface Condensation of Diboronic Acids

    ACS Nano · 2012 · 10.1021/nn302363d

  • Regio‐ and Chemoselective Metalation of Arenes and Heteroarenes Using Hindered Metal Amide Bases

    Angewandte Chemie International Edition · 2011 · 10.1002/anie.201101960

  • Synthesis of Well-Ordered COF Monolayers: Surface Growth of Nanocrystalline Precursors versus Direct On-Surface Polycondensation

    ACS Nano · 2011 · 10.1021/nn2032616

  • TMPZnCl·LiCl: A New Active Selective Base for the Directed Zincation of Sensitive Aromatics and Heteroaromatics

    Organic Letters · 2009 · 10.1021/ol900342a

  • Radical Catalysis of Kumada Cross‐Coupling Reactions Using Functionalized Grignard Reagents

    Angewandte Chemie International Edition · 2008 · 10.1002/anie.200803730

  • Convenient Preparation of Polyfunctional Aryl Magnesium Reagents by a Direct Magnesium Insertion in the Presence of LiCl

    Angewandte Chemie International Edition · 2008 · 10.1002/anie.200801968

  • Modern Amination Reactions

    European Journal of Organic Chemistry · 2007 · 10.1002/ejoc.200700391

  • Direct Magnesiation of Polyfunctionalized Arenes and Heteroarenes Using (tmp) 2 Mg⋅2 LiCl

    Angewandte Chemie International Edition · 2007 · 10.1002/anie.200701487

  • (tmp) 2 Zn⋅2 MgCl 2 ⋅2 LiCl: A Chemoselective Base for the Directed Zincation of Sensitive Arenes and Heteroarenes

    Angewandte Chemie International Edition · 2007 · 10.1002/anie.200701984

  • Gemischte Mg/Li‐Amide des Typs R2NMgCl⋅LiCl als hoch effiziente Basen zur regioselektiven Synthese funktionalisierter Aryl‐ und Heteroarylmagnesium‐Verbindungen

    Angewandte Chemie · 2006 · 10.1002/ange.200504024

  • Mixed Mg/Li Amides of the Type R 2 NMgCl⋅LiCl as Highly Efficient Bases for the Regioselective Generation of Functionalized Aryl and Heteroaryl Magnesium Compounds

    Angewandte Chemie International Edition · 2006 · https://doi.org/10.1002/anie.200504024

  • Soluble Lanthanide Salts (LnCl 3 ⋅2 LiCl) for the Improved Addition of Organomagnesium Reagents to Carbonyl Compounds

    Angewandte Chemie International Edition · 2006 · 10.1002/anie.200502485

  • Efficient Synthesis of Functionalized Organozinc Compounds by the Direct Insertion of Zinc into Organic Iodides and Bromides

    Angewandte Chemie International Edition · 2006 · 10.1002/anie.200601450

  • Practical Highly Enantioselective Synthesis of Propargylamines through a Copper‐Catalyzed One‐Pot Three‐Component Condensation Reaction

    Chemistry - A European Journal · 2006 · 10.1002/chem.200501233

  • Highly Efficient Reagents for Br/Mg Exchange

    Angewandte Chemie International Edition · 2005 · 10.1002/anie.200502220

  • A LiCl‐Mediated Br/Mg Exchange Reaction for the Preparation of Functionalized Aryl‐ and Heteroarylmagnesium Compounds from Organic Bromides

    Angewandte Chemie International Edition · 2004 · https://doi.org/10.1002/anie.200454084

  • Eine LiCl‐vermittelte Br/Mg‐Austauschreaktion zur Herstellung funktionalisierter Aryl‐ und Heteroarylmagnesium‐Verbindungen ausgehend von organischen Bromiden

    Angewandte Chemie · 2004 · 10.1002/ange.200454084

  • Enantioselective, Copper( I )‐Catalyzed Three‐Component Reaction for the Preparation of Propargylamines

    Angewandte Chemie International Edition · 2003 · 10.1002/anie.200352578

  • Synthese hoch funktionalisierter Organomagnesiumreagentien durch Halogen‐Metall‐Austausch

    Angewandte Chemie · 2003 · 10.1002/ange.200300579

  • Synthesis of polyfunctional indoles and related heterocycles mediated by cesium and potassium bases

    Tetrahedron · 2003 · 10.1016/s0040-4020(03)00073-5

  • Highly Functionalized Organomagnesium Reagents Prepared through Halogen–Metal Exchange

    Angewandte Chemie International Edition · 2003 · https://doi.org/10.1002/anie.200300579

  • Enantioselective Synthesis of Propargylamines by Copper-Catalyzed Addition of Alkynes to Enamines

    Angewandte Chemie International Edition · 2002 · 10.1002/1521-3773(20020715)41:14<2535::aid-anie2535>3.0.co;2-m

  • Nickel-Catalyzed Cross-Coupling between Functionalized Primary or Secondary Alkylzinc Halides and Primary Alkyl Halides

    The Journal of Organic Chemistry · 2001 · 10.1021/jo0105787

  • Versatile Indole Synthesis by a 5-endo-dig Cyclization Mediated by Potassium or Cesium Bases

    Angewandte Chemie International Edition · 2000 · 10.1002/1521-3773(20000717)39:14<2488::aid-anie2488>3.0.co;2-e

  • Copper-catalyzed aerobic oxidation of alcohols under fluorous biphasic conditions

    Tetrahedron Letters · 2000 · 10.1016/s0040-4039(00)00620-1

  • New Applications of Polyfunctional Organometallic Compounds in Organic Synthesis

    Angewandte Chemie International Edition · 2000 · 10.1002/1521-3773(20001215)39:24<4414::aid-anie4414>3.0.co;2-c

  • An Efficient Nickel-Catalyzed Cross-Coupling Between sp3 Carbon Centers

    Angewandte Chemie International Edition · 1998 · 10.1002/(sici)1521-3773(19980918)37:17<2387::aid-anie2387>3.0.co;2-m

  • Preparation of Highly Functionalized Grignard Reagents by an Iodine-Magnesium Exchange Reaction and its Application in Solid-Phase Synthesis

    Angewandte Chemie International Edition · 1998 · 10.1002/(sici)1521-3773(19980703)37:12<1701::aid-anie1701>3.0.co;2-u

  • Organozinc mediated reactions

    Tetrahedron · 1998 · 10.1016/s0040-4020(98)00318-4

  • A New Nickel‐Catalyzed Cross‐Coupling Reaction between sp 3 Carbon Centers

    Angewandte Chemie International Edition in English · 1996 · 10.1002/anie.199527231

  • Preparation and reactions of polyfunctional organozinc reagents in organic synthesis

    Chemical Reviews · 1993 · https://doi.org/10.1021/cr00022a008

  • Mild and stereoselective hydroborations of functionalized alkynes and alkenes using pinacolborane

    The Journal of Organic Chemistry · 1992 · 10.1021/jo00038a044

  • Preparation of functionalized dialkylzinc reagents via an iodine-zinc exchange reaction. Highly enantioselective synthesis of functionalized secondary alcohols

    The Journal of Organic Chemistry · 1992 · 10.1021/jo00033a008

  • Synthesis and reactivity toward acyl chlorides and enones of the new highly functionalized copper reagents RCu(CN)ZnI

    The Journal of Organic Chemistry · 1988 · 10.1021/jo00245a057

Current projects

    No projects listed.