Atroposelective total synthesis of axially chiral biaryl natural products G Bringmann, T Gulder, TAM Gulder, M Breuning Chemical reviews 111 (2), 563-639, 2011 | 1216 | 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 | 251 | 2016 |
Asymmetric synthesis: the essentials M Christmann, S Bräse Wiley-VCH, 2008 | 171 | 2008 |
Strained cyclophane natural products: macrocyclization at its limits T Gulder, PS Baran Natural Product Reports 29 (8), 899-934, 2012 | 152 | 2012 |
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 | 149 | 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 |
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 | 117 | 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 | 104 | 2016 |
A fluorination/aryl migration/cyclization cascade for the metal‐free synthesis of fluoro‐benzoxazepines A Ulmer, C Brunner, AM Arnold, A Pöthig, T Gulder Chemistry–A European Journal 22 (11), 3660-3664, 2016 | 101 | 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 | 96 | 2018 |
Biocatalysis fueled by light: on the versatile combination of photocatalysis and enzymes CJ Seel, T Gulder ChemBioChem 20 (15), 1871-1897, 2019 | 93 | 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 | 88 | 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 | 75 | 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 | 74 | 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 | 61 | 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 | 58 | 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 | 53 | 2016 |