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Organic Letters|September 21, 2016
Acid-Catalyzed Activation of Peroxyketals: Tunable Radical Initiation at Ambient Temperature and BelowBertrand Schweitzer-Chaput, Esther Boess, Martin Klussmann
Organic & Biomolecular Chemistry|January 22, 2011
Lewis acid-catalysed one pot synthesis of substituted xanthenesEsther Böss, Tim Hillringhaus, Jacqueline Nitsch, et al.
The Journal of Organic Chemistry|September 10, 2014
Reaction progress kinetic analysis of a copper-catalyzed aerobic oxidative coupling reaction with N-phenyl tetrahydroisoquinolineMartin Scott, Abhishek Sud, Esther Boess, et al.
Angewandte Chemie (International Ed. in English)|April 30, 2014
Acid-catalyzed oxidative radical addition of ketones to olefinsBertrand Schweitzer-Chaput, Joachim Demaerel, Hauke Engler, et al.
The Journal of Organic Chemistry|March 29, 2017
Reaction Mechanism of Iodine-Catalyzed Michael AdditionsDaniel von der Heiden, Seyma Bozkus, Martin Klussmann, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 2004
Helically chiral polymers: a class of ligands for asymmetric catalysisMichael Reggelin, Sebastian Doerr, Martin Klussmann, et al.
The Journal of Organic Chemistry|December 14, 2019
Investigating the Oxidation Step in the CuCl2-Catalyzed Aerobic Oxidative Coupling Reaction of N-Aryl TetrahydroisoquinolinesEsther Boess, Max Van Hoof, Sarah Luna Birdsall, et al.
Angewandte Chemie (International Ed. in English)|March 3, 2022
Formation of Breslow Intermediates from N-Heterocyclic Carbenes and Aldehydes Involves Autocatalysis by the Breslow Intermediate, and a HemiacetalAlina Wessels, Martin Klussmann, Martin Breugst, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|February 3, 2015
Experimental and computational studies on the C-H amination mechanism of tetrahydrocarbazoles via hydroperoxidesNaeem Gulzar, Kevin Mark Jones, Hannelore Konnerth, et al.
ACS Catalysis|January 25, 2024
Acid-Catalyzed Oxy-aminomethylation of StyrenesMarian Guillén, Sensheng Liu, C David Díaz-Oviedo, et al.
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