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Enantioselective Synthesis of Cyclopentenes by (3+2) Annulation via a 2‐Carbon Phosphonium.
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- Angewandte Chemie, 2024, v. 136, n. 35, p. 1, doi. 10.1002/ange.202408397
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Enantioselective Synthesis of Cyclopentenes by (3+2) Annulation via a 2‐Carbon Phosphonium.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 35, p. 1, doi. 10.1002/anie.202408397
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- Article
Pertechnetates – A Structural Study Across the Periodic Table.
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- Chemistry - A European Journal, 2024, v. 30, n. 26, p. 1, doi. 10.1002/chem.202400131
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Trendbericht Organische Chemie 2024.
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- Nachrichten aus der Chemie, 2024, v. 72, n. 3, p. 44, doi. 10.1002/nadc.20244139258
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- Article
Iodine‐Catalyzed Claisen‐Rearrangements of Allyl Aryl Ethers and Subsequent Iodocyclizations.
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- Chemistry - An Asian Journal, 2023, v. 18, n. 5, p. 1, doi. 10.1002/asia.202201279
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Trendbericht Organische Chemie 2023.
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- Nachrichten aus der Chemie, 2023, v. 71, n. 3, p. 40, doi. 10.1002/nadc.20234135542
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Stereoselective Synthesis of 2‐Oxyenamides**.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 31, p. 1, doi. 10.1002/ejoc.202200772
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- Article
Die Bildung von Breslow‐Intermediaten aus N‐heterocyclischen Carbenen und Aldehyden verläuft autokatalytisch und mit einem Halbacetal als Intermediat.
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- Angewandte Chemie, 2022, v. 134, n. 23, p. 1, doi. 10.1002/ange.202117682
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Innenrücktitelbild: Die Bildung von Breslow‐Intermediaten aus N‐heterocyclischen Carbenen und Aldehyden verläuft autokatalytisch und mit einem Halbacetal als Intermediat (Angew. Chem. 23/2022).
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- Angewandte Chemie, 2022, v. 134, n. 23, p. 1, doi. 10.1002/ange.202205351
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Formation of Breslow Intermediates from N‐Heterocyclic Carbenes and Aldehydes Involves Autocatalysis by the Breslow Intermediate, and a Hemiacetal.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 23, p. 1, doi. 10.1002/anie.202117682
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Inside Back Cover: Formation of Breslow Intermediates from N‐Heterocyclic Carbenes and Aldehydes Involves Autocatalysis by the Breslow Intermediate, and a Hemiacetal (Angew. Chem. Int. Ed. 23/2022).
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- Angewandte Chemie International Edition, 2022, v. 61, n. 23, p. 1, doi. 10.1002/anie.202205351
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- Article
Trendbericht Organische Chemie 2022.
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- Nachrichten aus der Chemie, 2022, v. 70, n. 3, p. 42, doi. 10.1002/nadc.20224122453
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- Article
Ammonium Pertechnetate in Mixtures of Trifluoromethanesulfonic Acid and Trifluoromethanesulfonic Anhydride.
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- Angewandte Chemie, 2022, v. 134, n. 3, p. 1, doi. 10.1002/ange.202113777
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Ammonium Pertechnetate in Mixtures of Trifluoromethanesulfonic Acid and Trifluoromethanesulfonic Anhydride.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 3, p. 1, doi. 10.1002/anie.202113777
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- Article
Some Surprising Transformations of Colchicone and Other Colchicine‐Derived Tropolones.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 46, p. 6375, doi. 10.1002/ejoc.202100999
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- Article
Iodine‐Catalyzed Diels‐Alder Reactions.
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- ChemCatChem, 2021, v. 13, n. 12, p. 2922, doi. 10.1002/cctc.202100342
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- Article
Cover Feature: Breslow Intermediates (Amino Enols) and Their Keto Tautomers: First Gas‐Phase Characterization by IR Ion Spectroscopy (Chem. Eur. J. 8/2021).
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- Chemistry - A European Journal, 2021, v. 27, n. 8, p. 2552, doi. 10.1002/chem.202004678
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- Article
Breslow Intermediates (Amino Enols) and Their Keto Tautomers: First Gas‐Phase Characterization by IR Ion Spectroscopy.
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- Chemistry - A European Journal, 2021, v. 27, n. 8, p. 2662, doi. 10.1002/chem.202003454
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- Article
Experimental and Computational Investigations of the Reactions between α,β‐Unsaturated Lactones and 1,3‐Dienes by Cooperative Lewis Acid/Brønsted Acid Catalysis.
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- Angewandte Chemie, 2020, v. 132, n. 42, p. 18868, doi. 10.1002/ange.202008365
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Experimental and Computational Investigations of the Reactions between α,β‐Unsaturated Lactones and 1,3‐Dienes by Cooperative Lewis Acid/Brønsted Acid Catalysis.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 42, p. 18709, doi. 10.1002/anie.202008365
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Front Cover: σ‐Hole Interactions in Catalysis (Eur. J. Org. Chem. 34/2020).
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 34, p. 5471, doi. 10.1002/ejoc.202001150
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σ‐Hole Interactions in Catalysis.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 34, p. 5473, doi. 10.1002/ejoc.202000660
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- Article
Die Huisgen‐Reaktion: Meilensteine der 1,3‐dipolaren Cycloaddition.
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- Angewandte Chemie, 2020, v. 132, n. 30, p. 12389, doi. 10.1002/ange.202003115
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The Huisgen Reaction: Milestones of the 1,3-Dipolar Cycloaddition.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 30, p. 12293, doi. 10.1002/anie.202003115
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- Article
Identification of N‐ or O‐Alkylation of Aromatic Nitrogen Heterocycles and N‐Oxides Using <sup>1</sup>H–<sup>15</sup>N HMBC NMR Spectroscopy.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 22, p. 3270, doi. 10.1002/ejoc.202000329
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- Article
Chemie, Köln und Karneval.
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- Nachrichten aus der Chemie, 2020, v. 68, n. 5, p. 90, doi. 10.1002/nadc.20204098984
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Synthesis of the 8,19‐Epoxysteroid Eurysterol A.
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- Chemistry - A European Journal, 2020, v. 26, n. 19, p. 4256, doi. 10.1002/chem.202000585
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- Article
N‐Heterocyclic Carbene Catalyzed (5+1) Annulations Exploiting a Vinyl Dianion Synthon Strategy.
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- Angewandte Chemie, 2019, v. 131, n. 33, p. 11607, doi. 10.1002/ange.201905475
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N‐Heterocyclic Carbene Catalyzed (5+1) Annulations Exploiting a Vinyl Dianion Synthon Strategy.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 33, p. 11483, doi. 10.1002/anie.201905475
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Philicity of Acetonyl and Benzoyl Radicals: A Comparative Experimental and Computational Study.
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- Chemistry - A European Journal, 2019, v. 25, n. 38, p. 9088, doi. 10.1002/chem.201901439
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Intermediates of N‐Heterocyclic Carbene (NHC) Dimerization Probed in the Gas Phase by Ion Mobility Mass Spectrometry: C−H⋅⋅⋅:C Hydrogen Bonding Versus Covalent Dimer Formation.
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- Chemistry - A European Journal, 2019, v. 25, n. 10, p. 2511, doi. 10.1002/chem.201803641
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Reaktionen im kontinuierlichen Strom.
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- Nachrichten aus der Chemie, 2019, v. 67, n. 1, p. 81, doi. 10.1002/nadc.20194084228
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Synthese im Blickpunkt: Katalyse mit elektrophilen Phosphoniumkationen.
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- Nachrichten aus der Chemie, 2018, v. 66, n. 9, p. 862, doi. 10.1002/nadc.20184077309
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- Article
Frontispiece: Mechanisms in Iodine Catalysis.
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- Chemistry - A European Journal, 2018, v. 24, n. 37, p. 1, doi. 10.1002/chem.201883762
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Mechanisms in Iodine Catalysis.
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- Chemistry - A European Journal, 2018, v. 24, n. 37, p. 9187, doi. 10.1002/chem.201706136
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- Article
Front Cover: Regioselective 1,3‐Dipolar Cycloadditions of Diazoalkanes with Heteroatom‐Substituted Alkynes: Theory and Experiment (Eur. J. Org. Chem. 20‐21/2018).
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 20/21, p. 2294, doi. 10.1002/ejoc.201800739
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- Article
Regioselective 1,3‐Dipolar Cycloadditions of Diazoalkanes with Heteroatom‐Substituted Alkynes: Theory and Experiment.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 20/21, p. 2477, doi. 10.1002/ejoc.201800100
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- Article
Köln: Wissenschaft an Karneval.
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- Nachrichten aus der Chemie, 2018, v. 66, n. 6, p. 641, doi. 10.1002/nadc.20184075156
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Sperrige Substituenten – Zwischen Attraktion und Repulsion.
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- Nachrichten aus der Chemie, 2018, v. 66, n. 5, p. 505, doi. 10.1002/nadc.20184073225
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- Article
Highly Enantioselective Allylation of Ketones: An Efficient Approach to All Stereoisomers of Tertiary Homoallylic Alcohols.
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- Chemistry - A European Journal, 2017, v. 23, n. 50, p. 12136, doi. 10.1002/chem.201701740
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Redox-Neutral Aromatization of Cyclic Amines: Mechanistic Insights and Harnessing of Reactive Intermediates for Amine α- and β-C−H Functionalization.
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- Chemistry - A European Journal, 2016, v. 22, n. 50, p. 18179, doi. 10.1002/chem.201603839
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Quantification of the.
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- Journal of Physical Organic Chemistry, 2016, v. 29, n. 12, p. 759, doi. 10.1002/poc.3580
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Enantioselektive Katalysatoren zur Synthese von α-substituierten Allylboronsäureestern - ein effizienter Zugang zu isomerenreinen Homoallylalkoholen.
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- Angewandte Chemie, 2016, v. 128, n. 4, p. 1574, doi. 10.1002/ange.201509198
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Enantioselective Catalysts for the Synthesis of α-Substituted Allylboronates-An Accelerated Approach towards Isomerically Pure Homoallylic Alcohols.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 4, p. 1548, doi. 10.1002/anie.201509198
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Mit molekularem Iod katalysieren.
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- Nachrichten aus der Chemie, 2015, v. 63, n. 12, p. 1180, doi. 10.1002/nadc.201590404
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Experimental and Computational Studies on the CH Amination Mechanism of Tetrahydrocarbazoles via Hydroperoxides.
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- Chemistry - A European Journal, 2015, v. 21, n. 8, p. 3367, doi. 10.1002/chem.201405376
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Nucleophilic Reactivities of the Anions of Nucleobases and Their Subunits.
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- Chemistry - A European Journal, 2012, v. 18, n. 1, p. 127, doi. 10.1002/chem.201102411
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N-Heterocyclische Carbene: Organokatalysatoren mit mäßiger Nucleophilie, aber außerordentlich hoher Lewis-Basizität.
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- Angewandte Chemie, 2011, v. 123, n. 30, p. 7047, doi. 10.1002/ange.201102435
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N-Heterocyclic Carbenes: Organocatalysts with Moderate Nucleophilicity but Extraordinarily High Lewis Basicity.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 30, p. 6915, doi. 10.1002/anie.201102435
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Abschied vom HSAB-Modell ambidenter Reaktivität.
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- Angewandte Chemie, 2011, v. 123, n. 29, p. 6598, doi. 10.1002/ange.201007100
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- Article