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Acta Crystallographica. Section E, Crystallographic Communications|August 18, 2018
Redetermination of the solvent-free crystal structure of l-prolineJonas J Koenig, Jörg-M Neudörfl, Anne Hansen, et al.
The Journal of Organic Chemistry|April 29, 2022
pH-Controlled Intramolecular Decarboxylative Cyclization of Biarylacetic Acids: Implication on Umpolung Reactivity of Aroyl RadicalsJoydev K Laha, Upma Gulati, Saima, 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.
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.
Organic Letters|July 20, 2016
Influence of the N-Substituents on the Nucleophilicity and Lewis Basicity of N-Heterocyclic CarbenesAlison Levens, Feng An, Martin Breugst, et al.
The Journal of Organic Chemistry|March 27, 2014
δ-Deuterium isotope effects as probes for transition-state structures of isoprenoid substratesSeoung-ryoung Choi, Martin Breugst, Kendall N Houk, et al.
The Journal of Organic Chemistry|June 27, 2019
Ambident Reactivity of Phenolate Anions Revisited: A Quantitative Approach to Phenolate ReactivitiesRobert J Mayer, Martin Breugst, Nathalie Hampel, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|April 20, 2017
Highly Enantioselective Allylation of Ketones: An Efficient Approach to All Stereoisomers of Tertiary Homoallylic AlcoholsMarcus Brauns, Marvin Mantel, Julie Schmauck, et al.
The Journal of Organic Chemistry|June 13, 2019
Iodine-Catalyzed Nazarov CyclizationsJonas J Koenig, Thiemo Arndt, Nora Gildemeister, et al.
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