Publications

Desyl and Phenacyl as Versatile, Photocatalytically Cleavable Protecting Groups - A Classic Approach in a Different (Visible) Light

Elisabeth Speckmeier and Kirsten Zeitler, ACSCatal. 2017, 7, 6821-6826.
Web edition: http://dx.doi.org./10.1021/acscatal.7b02117

Nitroalkenes as latent 1,2-biselectrophiles - A multicatalytic approach for the synthesis of 1,4-diketones and their application in a 4-step one-pot reaction to polysubstituted pyrroles

Patrick J. W. Fuchs and Kirsten Zeitler, J. Org. Chem. 2017, 82, 7796–7805.
Web edition: http://dx.doi.org./10.1021/acs.joc.7b00830

Carboranes as Aryl Mimetics in Catalysis: a Highly Active Zwitterionic NHC Precatalyst

Christoph Selg, Wilma Neumann, Peter Lönnecke, Evamarie Hey-Hawkins and Kirsten Zeitler, Chem. Eur. J. 2017, 23, 7932-7937.
Web edition: http://dx.doi.org./10.1002/chem.201700209

Domino reactions: More than just a game

T. Broja, P. J. W. Fuchs, K. Zeitler, Nat. Chem. 2015, 7, 950.
Web edition: http://dx.doi.org./10.1038/nchem.2402

Visible Light Mediated Reductive Cleavage of C–O Bonds Accessing α-Substituted Aryl Ketones

Elisabeth Speckmeier, Clément Padié, Kirsten Zeitler, Org. Lett. 2015, 17, 4818-4821.
Web edition: http://dx.doi.org./10.1021/acs.orglett.5b02378 

No Photocatalyst Required – Versatile, Visible Light Mediated Transformations with Polyhalomethanes

Johannes F. Franz, Wolfgang B. Kraus, Kirsten Zeitler, Chem. Commun. 2015, 51, 8280-8283.
Web edition: http://dx.doi.org./10.1039/C4CC10270C

Aerobic oxidation of NHC-catalysed aldehyde esterifications with alcohols: benzoin, not the Breslow intermediate, undergoes oxidation

Eoghan G. Delany, Claire-Louise Fagan, Sivaji Gundala, Kirsten Zeitler and Stephen J. Connon, Chem. Commun. 2013, 49, 6513-6515.
Web edition: http://dx.doi.org./10.1039/C3CC42597E

NHC-catalysed aerobic aldehyde-esterifications with alcohols: no additives or cocatalysts required

Eoghan G. Delany, Claire-Louise Fagan, Sivaji Gundala, Alessandra Mari, Thomas Broja, Kirsten Zeitler and Stephen J. Connon, Chem. Commun. 2013, 49, 6510-6512.
Web edition: http://dx.doi.org/10.1039/C3CC42596G

A Cooperative Hydrogen-Bond-Promoted Organophotoredox Catalysis Strategy for Highly Diastereoselective, Reductive Enone Cyclization

Matthias Neumann and Kirsten Zeitler, Chem. Eur. J. 2013, 19, 6950-6955.
Web edition: http://dx.doi.org/10.1002/chem.201204573

What is your actual catalyst? TMS cleavage rates of diarylprolinol silyl ethers studied by in situ NMR

Michael H. Haindl, Markus B. Schmid, Kirsten Zeitler and Ruth M. Gschwind, RSC Adv. 2012, 2, 5941-5943.
Web edition: http://dx.doi.org/10.1039/C2RA20860A

Application of microflow conditions to visible light photoredox catalysis

Matthias Neumann and Kirsten Zeitler, Org. Lett. 2012, 14, 2658-2661.
Web edition: http://dx.doi.org/10.1021/ol3005529

NHC-catalyzed, chemoselective crossed-acyloin reactions

Christopher A. Rose, Sivaji Gundala, Claire-Louise Fagan, Johannes F. Franz, Stephen J. Connon and Kirsten Zeitler, Chem. Sci. 2012, 3, 735-740.
Web edition: http://dx.doi.org/10.1039/C2SC00622G

Stabilization of Proline Enamine Carboxylates by Amine Bases

Markus B. Schmid, Kirsten Zeitler, Ruth M. Gschwind, Chem. Eur. J. 2012, 18, 3362–3370.
Web edition: http://dx.doi.org/10.1002/chem.201102660

A novel reaction-based, chromogenic and "turn-on" fluorescent chemodosimeter for fluoride detection

Clément Padié and Kirsten Zeitler, New J. Chem. 2011, 35, 994-997.
Web edition: http://dx.doi.org/10.1039/C0NJ00937G

A versatile combined N-heterocyclic carbene and base-catalyzed multiple cascade approach for the synthesis of functionalized benzofuran-3-(2H)-ones

Johannes F. Franz, Patrick J. W. Fuchs and Kirsten Zeitler, Tetrahedron Lett. 2011, 52, 6952-6956.
Web edition: http://dx.doi.org/10.1016/j.tetlet.2011.10.078

Highlighted in ChemInform 2012, as Editors´Choice

Chemoselective crossed acyloin condensations: catalyst and substrate control

Christopher A. Rose, Sivaji Gundala, Stephen J. Connon and Kirsten Zeitler, Synthesis 2011, 2, 190-198.
Web edition: http://dx.doi.org/10.1055/s-0030-1258363

Highly Chemoselective Direct Crossed Aliphatic-Aromatic Acyloin Condensations with Triazolium-Derived Carbene Catalysts

Sarah E. O'Toole, Christopher A. Rose, Sivaji Gundala, Kirsten Zeitler and Stephen J. Connon, J. Org. Chem. 2011, 76, 347-357.
Web edition: http://dx.doi.org/10.1021/jo101791w

Featured Article with Cover Picture

Formation and Stability of Prolinol and Prolinol Ether Enamines by NMR: Delicate Selectivity and Reactivity Balances and Parasitic Equilibria

Markus B. Schmid, Kirsten Zeitler and Ruth M. Gschwind, J. Am. Chem. Soc. 2011, 133, 7065–7074.
Web edition: http://dx.doi.org/10.1021/ja111544b

NMR Investigations on the Proline-Catalyzed Aldehyde Self-Condensation: Mannich Mechanism, Dienamine Detection, and Erosion of the Aldol Addition Selectivity

Markus B. Schmid, Kirsten Zeitler and Ruth M. Gschwind, J. Org. Chem. 2011, 76, 3005–3015.
Web edition: http://dx.doi.org/10.1021/jo200431v

Metal-Free, Cooperative Asymmetric Organophotoredox Catalysis with Visible Light

Matthias Neumann, Stefan Füldner, Burkhard König, Kirsten Zeitler, Angew. Chem. Int. Ed. 2011, 50, 951-954.
Web edition: http://dx.doi.org/10.1002/anie.201002992

Cover Picture: http://dx.doi.org/10.1002/anie.201006295
Highlighted in Synfacts 2010, 1419: "Organophotoredox Catalysis" - Synfact of the Month

Efficient Catalytic, Oxidative Lactonization for the Synthesis of Benzodioxepinones using Thiazolium Derived Carbene Catalysts

Christopher A. Rose, Kirsten Zeitler, Org. Lett. 2010, 12, 4552-4555.
Web edition: http://dx.doi.org/10.1021/ol101854r

Efficient, Enantioselective Iminium Catalysis with an Immobilized, Recyclable Diarylprolinol Silyl Ether Catalyst

Ina Mager, Kirsten Zeitler, Org. Lett. 2010, 12, 1480-1483.
Web edition: http://dx.doi.org/10.1021/ol100166z

Photoredox Catalysis with Visible Light

Kirsten Zeitler, Angew. Chem. Int. Ed. 2009, 48, 9785-9789.
Web edition: http://dx.doi.org/10.1002/anie.200904056

Highly Enantioselective Benzoin Condensation Reactions Involving a Bifunctional Protic Pentafluorophenyl-Substituted Triazolium Precatalyst

Louise Baragwanath, Christopher A. Rose, Kirsten Zeitler, Stephen J. Connon, J. Org. Chem. 2009, 74, 9214-9217.
Web edition: http://dx.doi.org/10.1021/jo902018j

An Efficient Carbene-Catalyzed Access to 3,4-Dihydrocoumarins

Kirsten Zeitler, Christopher A. Rose, J. Org. Chem. 2009, 74, 1759-1762.
Web edition: http://dx.doi.org/10.1021/jo802285r

N-Heterocyclic Carbenes - Organocatalysts Displaying Diverse Modes of Action

Kirsten Zeitler, E. Schering Found. Symp. Proc. 2007, 2, 183-206.

Asymmetric Organocatalysis

Stefan Jaroch, Hilmar Weinmann, Kirsten Zeitler, ChemMedChem 2007, 2, 1261-1264.
Web edition: http://dx.doi.org/10.1002/cmdc.200700109

An Efficient and Versatile Approach for the Immobilization of Carbene Precursors via Copper-catalyzed [3+2]-Cycloaddition and their Catalytic Application

Kirsten Zeitler, Ina Mager, Adv. Synth. Cat. 2007, 349, 1851-1857.
Web edition: http://dx.doi.org/10.1002/adsc.200700174

Highlighted in Synfacts 2007, 1221: "MeOPEG-Supported Carbene Catalysts"

Stereoselective Synthesis of (E)-α,β-Unsaturated Esters via Carbene-Catalyzed Redox Esterification

Kirsten Zeitler, Org. Lett. 2006, 8, 637-640.
Web edition: http://dx.doi.org/10.1021/ol052826h

Extending Mechanistic Routes in Heterazolium Catalysis-Promising Concepts for Versatile Synthetic Methods

Kirsten Zeitler, Angew. Chem. Int. Ed. 2005, 44, 7506-7510.
Web edition: http://dx.doi.org/10.1002/anie.200502617

letzte Änderung: 13.09.2017