| Atroposelective total synthesis of axially chiral biaryl natural products G Bringmann, T Gulder, TAM Gulder, M Breuning Chemical reviews 111 (2), 563-639, 2011 | 1176 | 2011 |
| Hypervalent iodine (III) fluorinations of alkenes and diazo compounds: new opportunities in fluorination chemistry SV Kohlhepp, T Gulder Chemical Society Reviews 45 (22), 6270-6288, 2016 | 233 | 2016 |
| Asymmetric synthesis: the essentials M Christmann, S Bräse Wiley-VCH, 2008 | 186 | 2008 |
| Strained cyclophane natural products: macrocyclization at its limits T Gulder, PS Baran Natural Product Reports 29 (8), 899-934, 2012 | 147 | 2012 |
| The online assignment of the absolute configuration of natural products: HPLC‐CD in combination with quantum chemical CD calculations G Bringmann, TAM Gulder, M Reichert, T Gulder Chirality: The Pharmacological, Biological, and Chemical Consequences of …, 2008 | 146 | 2008 |
| Metal-free synthesis of 3, 3-disubstituted oxoindoles by iodine (III)-catalyzed bromocarbocyclizations. DC Fabry, M Stodulski, S Hoerner, T Gulder Chemistry (Weinheim an der Bergstrasse, Germany) 18 (35), 10834-10838, 2012 | 145 | 2012 |
| The antimicrobial peptide cathelicidin interacts with airway mucus K Felgentreff, C Beisswenger, M Griese, T Gulder, G Bringmann, R Bals Peptides 27 (12), 3100-3106, 2006 | 119 | 2006 |
| Activities of Naphthylisoquinoline Alkaloids and Synthetic Analogs against Leishmania major A Ponte-Sucre, JH Faber, T Gulder, I Kajahn, SEH Pedersen, ... Antimicrobial agents and chemotherapy 51 (1), 188-194, 2007 | 114 | 2007 |
| Ancistrocladinium A and B, the First N,C-Coupled Naphthyldihydroisoquinoline Alkaloids, from a Congolese Ancistrocladus Species G Bringmann, I Kajahn, M Reichert, SEH Pedersen, JH Faber, T Gulder, ... The Journal of Organic Chemistry 71 (25), 9348-9356, 2006 | 111 | 2006 |
| Advances in Iodine (III)‐Mediated Halogenations: A Versatile Tool to Explore New Reactivities and Selectivities AM Arnold, A Ulmer, T Gulder Chemistry–A European Journal 22 (26), 8728-8739, 2016 | 100 | 2016 |
| A fluorination/aryl migration/cyclization cascade for the metal‐free synthesis of fluoro‐benzoxazepines A Ulmer, C Brunner, AM Arnold, A Poethig, T Gulder Chemistry–A European Journal 22 (11), 3660-3664, 2016 | 95 | 2016 |
| NXS, Morpholine, and HFIP: The Ideal Combination for Biomimetic Haliranium-Induced Polyene Cyclizations AM Arnold, A Pöthig, M Drees, T Gulder Journal of the American Chemical Society 140 (12), 4344-4353, 2018 | 92 | 2018 |
| Biocatalysis fueled by light: on the versatile combination of photocatalysis and enzymes CJ Seel, T Gulder ChemBioChem 20 (15), 1871-1897, 2019 | 90 | 2019 |
| Ancisheynine, the First N,C-Coupled Naphthylisoquinoline Alkaloid: Total Synthesis and Stereochemical Analysis G Bringmann, T Gulder, M Reichert, F Meyer Organic letters 8 (6), 1037-1040, 2006 | 85 | 2006 |
| Halocarbocyclization versus dihalogenation: substituent directed iodine (III) catalyzed halogenations M Stodulski, A Goetzinger, SV Kohlhepp, T Gulder Chemical communications 50 (26), 3435-3438, 2014 | 73 | 2014 |
| Total Synthesis of the N,C-Coupled Naphthylisoquinoline Alkaloids Ancistrocladinium A and B and Related Analogues G Bringmann, T Gulder, B Hertlein, Y Hemberger, F Meyer Journal of the American Chemical Society 132 (3), 1151-1158, 2010 | 73 | 2010 |
| Structure−Activity Relationship and Studies on the Molecular Mechanism of Leishmanicidal N,C-Coupled Arylisoquinolinium Salts A Ponte-Sucre, T Gulder, A Wegehaupt, C Albert, C Rikanovic, ... Journal of medicinal chemistry 52 (3), 626-636, 2009 | 59 | 2009 |
| Fluorine as a traceless directing group for the regiodivergent synthesis of indoles and tryptophans A Andries-Ulmer, C Brunner, J Rehbein, T Gulder Journal of the American Chemical Society 140 (40), 13034-13041, 2018 | 56 | 2018 |
| Atom‐Economic Electron Donors for Photobiocatalytic Halogenations CJ Seel, A Králík, M Hacker, A Frank, B König, T Gulder ChemCatChem 10 (18), 3960-3963, 2018 | 53 | 2018 |
| Characterization of a cyanobacterial haloperoxidase and evaluation of its biocatalytic halogenation potential A Frank, CJ Seel, M Groll, T Gulder ChemBioChem 17 (21), 2028-2032, 2016 | 52 | 2016 |
