M. Sc. Lisa Marie Kammer

Institute of Organic Chemistry
Johannes Gutenberg-University Mainz
Duesbergweg 10-14, 55128 Mainz
Room 2.223/01-124
Phone (06131) 39-22364
E-mail kammer[at]uni-mainz.de
Research interests: Method development, photoredox catalysis, green chemistry, functionalization of amino acids, aryne chemsitry, functionalization and synthesis of heterocycles
Publications:

Photoredox-Catalyzed Four Component Reaction for the Synthesis of Complex Secondary Amines

L. M. Kammer, M. Krumb, B. Spitzbarth, B. Lipp, J. Kühlborn, J. Busold, O. M. Mulina, A. O. Terentev and T. Opatz, Org. Lett. 2020, 22, 3318−3322. (Back Cover)

Visible Light-Induced Cleavage of C–S bonds in Thioacetals and Thioketals with Iodine as a Photocatalyst
M. Krumb, L. M. Kammer, R. Forster, C. Grundke, T. Opatz, ChemPhotoChem. 20204, 101 – 104.
This article was selected as Very Important Paper and also appears in: Hot Topic: Photocatalysis and Special collection: Photochemical Synthesis. (Cover Picture)

Deaminative Reductive Arylation Enabled by Nickel/Photoredox Dual Catalysis
J. Yi, S. O. Badir, L. M. Kammer, M. Ribagorda, G. A. Molander, Org. Lett. 2019, Article ASAP.

Visible Light-Induced Sulfonylation/Arylation of Styrenes in a Double Radical Three-Component Photoredox Reaction
B. Lipp, L. M. Kammer, M. Kücükdisli, A. Luque, J. Kühlborn,
S. Pusch, G. Matulevičiūtė, D. Schollmeyer, A. Šačkus, T. Opatz, Chem. Eur. J. 2019, 8965–8969.
(Hot Paper) (cover picture)

Photoredox-Alkenylation of Carboxylic Acids and Peptides: Synthesis of Covalent Enzyme Inhibitors
L. M. Kammer, B. Lipp, T. Opatz, J. Org. Chem., 2019, 84 (5), 2379–2392.
Article was selected for "ACS Editors' Choice" (View ACS LiveSlides presentation, Front Cover).

Visible Light Driven Minisci-Type Reaction with N-Hydroxyphthalimide Esters
L. Kammer, A. Rahman, T. Opatz, Molecules 2018, 23, 764.

One-pot Synthesis of Pyrrole-2-carboxylates and -carboxamides via an Electrocyclization/Oxidation Sequence
D. Imbri, N. Netz, M. Kücükdisli, L. Kammer, P. Jung, A. Kretzschmann, T. Opatz, J. Org. Chem. 2014, 79, 11750–11758.