| Year |
Citation |
Score |
| 2022 |
Flegel J, Shaaban S, Jia ZJ, Schulte B, Lian Y, Krzyzanowski A, Metz M, Schneidewind T, Wesseler F, Flegel A, Reich A, Brause A, Xue G, Zhang M, Dötsch L, ... ... Antonchick AP, et al. The Highly Potent AhR Agonist Picoberin Modulates Hh-Dependent Osteoblast Differentiation. Journal of Medicinal Chemistry. PMID 36459434 DOI: 10.1021/acs.jmedchem.2c00956 |
0.546 |
|
| 2022 |
Hui C, Craggs L, Antonchick AP. Ring contraction in synthesis of functionalized carbocycles. Chemical Society Reviews. 51: 8652-8675. PMID 36172989 DOI: 10.1039/d1cs01080h |
0.332 |
|
| 2022 |
Hui C, Antonchick AP. Concise synthesis of piperarborenine B. Bioorganic & Medicinal Chemistry. 67: 116817. PMID 35609467 DOI: 10.1016/j.bmc.2022.116817 |
0.375 |
|
| 2022 |
Waldmann H, Akbarzadeh M, Flegel J, Patil S, Shang E, Narayan R, Buchholzer M, Jasemi NSK, Grigalunas M, Krzyzanowski A, Abegg D, Shuster A, Potowski M, Karatas H, Karageorgis G, ... ... Antonchick AP, et al. The Pseudo-Natural Product Rhonin Targets RHOGDI. Angewandte Chemie (International Ed. in English). PMID 35170181 DOI: 10.1002/anie.202115193 |
0.771 |
|
| 2022 |
Wesseler F, Riege D, Puthanveedu M, Halver J, Müller E, Bertrand J, Antonchick AP, Sievers S, Waldmann H, Schade D. Probing Embryonic Development Enables the Discovery of Unique Small-Molecule Bone Morphogenetic Protein Potentiators. Journal of Medicinal Chemistry. PMID 35108017 DOI: 10.1021/acs.jmedchem.1c01800 |
0.514 |
|
| 2021 |
Hui C, Brieger L, Strohmann C, Antonchick AP. Stereoselective Synthesis of Cyclobutanes by Contraction of Pyrrolidines. Journal of the American Chemical Society. PMID 34748319 DOI: 10.1021/jacs.1c10175 |
0.397 |
|
| 2021 |
Polychronidou V, Krupp A, Strohmann C, Antonchick AP. Cascade aza-Wittig/6π-Electrocyclization in the Synthesis of 1,6-Dihydropyridines. Organic Letters. PMID 34291925 DOI: 10.1021/acs.orglett.1c02099 |
0.441 |
|
| 2021 |
Waldmann H, Yildirim O, Grigalunas M, Brieger L, Strohmann C, Antonchick AP. Dynamic Catalytic Highly Enantioselective 1,3-Dipolar Cycloadditions. Angewandte Chemie (International Ed. in English). PMID 34236754 DOI: 10.1002/anie.202108072 |
0.603 |
|
| 2021 |
Puthanveedu M, Khamraev V, Brieger L, Strohmann C, Antonchick AP. Electrochemical Dehydrogenative C(sp )-H Amination. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33931904 DOI: 10.1002/chem.202100960 |
0.42 |
|
| 2021 |
Grigalunas M, Burhop A, Zinken S, Pahl A, Gally JM, Wild N, Mantel Y, Sievers S, Foley DJ, Scheel R, Strohmann C, Antonchick AP, Waldmann H. Natural product fragment combination to performance-diverse pseudo-natural products. Nature Communications. 12: 1883. PMID 33767198 DOI: 10.1038/s41467-021-22174-4 |
0.536 |
|
| 2020 |
Shaaban S, Li H, Otte F, Strohmann C, Antonchick AP, Waldmann H. Enantioselective Synthesis of Five-Membered-Ring Atropisomers with a Chiral Rh(III) Complex. Organic Letters. PMID 33186042 DOI: 10.1021/acs.orglett.0c03355 |
0.625 |
|
| 2019 |
Puthanveedu M, Polychronidou V, Antonchick AP. Catalytic Selective Metal-Free Cross-Coupling of Heteroaromatic N-Oxides with Organosilanes. Organic Letters. 21: 3407-3411. PMID 31013107 DOI: 10.1021/Acs.Orglett.9B01141 |
0.51 |
|
| 2019 |
Bering L, Antonchick AP. Reactive nitrogen species: Nitrosonium ions in organic synthesis Tetrahedron. 75: 1131-1143. DOI: 10.1016/J.Tet.2019.01.036 |
0.448 |
|
| 2018 |
Schneidewind T, Kapoor S, Garivet G, Karageorgis G, Narayan R, Vendrell-Navarro G, Antonchick AP, Ziegler S, Waldmann H. The Pseudo Natural Product Myokinasib Is a Myosin Light Chain Kinase 1 Inhibitor with Unprecedented Chemotype. Cell Chemical Biology. PMID 30686759 DOI: 10.1016/J.Chembiol.2018.11.014 |
0.743 |
|
| 2018 |
Li H, Gontla R, Flegel J, Merten C, Ziegler S, Antonchick AP, Waldmann H. Enantioselective Formal C(sp )-H Bond Activation in the Synthesis of Bioactive Spiropyrazolone Derivatives. Angewandte Chemie (International Ed. in English). PMID 30511449 DOI: 10.1002/Anie.201811041 |
0.68 |
|
| 2018 |
Bering L, D'Ottavio L, Sirvinskaite G, Antonchick AP. Nitrosonium ion catalysis: aerobic, metal-free cross-dehydrogenative carbon-heteroatom bond formation. Chemical Communications (Cambridge, England). 54: 13022-13025. PMID 30403232 DOI: 10.1039/C8Cc08328B |
0.507 |
|
| 2018 |
Waldmann H, Shan G, Flegel J, Li H, Merten C, Ziegler S, Antonchick AP. C-H Bond Activation for the Synthesis of Heterocyclic Atropisomers Yields Hedgehog Pathway Inhibitors. Angewandte Chemie (International Ed. in English). PMID 30203905 DOI: 10.1002/Anie.201809680 |
0.68 |
|
| 2018 |
Manna S, Antonchick AP. Catalytic Transfer Hydrogenation Using Biomass as Hydrogen Source. Chemsuschem. PMID 30073788 DOI: 10.1002/Cssc.201801770 |
0.748 |
|
| 2018 |
Bering L, Vogt M, Paulussen FM, Antonchick AP. Selective, Catalytic, and Metal-Free Coupling of Electron-Rich Phenols and Anilides Using Molecular Oxygen as Terminal Oxidant. Organic Letters. PMID 29927252 DOI: 10.1021/Acs.Orglett.8B01631 |
0.481 |
|
| 2018 |
Bering L, Jeyakumar K, Antonchick AP. Metal-Free C-O Bond Functionalization: Catalytic Intramolecular and Intermolecular Benzylation of Arenes. Organic Letters. PMID 29902015 DOI: 10.1021/Acs.Orglett.8B01495 |
0.508 |
|
| 2018 |
Utepova IA, Serebrennikova PO, Streltsova MS, Musikhina AA, Fedorchenko TG, Chupakhin ON, Antonchick AP. Enantiomerically Enriched 1,2-,-Bidentate Ferrocenyl Ligands for 1,3-Dipolar Cycloaddition and Transfer Hydrogenation Reactions. Molecules (Basel, Switzerland). 23. PMID 29848984 DOI: 10.3390/Molecules23061311 |
0.457 |
|
| 2018 |
Bering L, Paulussen FM, Antonchick AP. Aerobic, Metal-Free, and Catalytic Dehydrogenative Coupling of Heterocycles: En Route to Hedgehog Signaling Pathway Inhibitors. Organic Letters. PMID 29547297 DOI: 10.1021/Acs.Orglett.8B00521 |
0.462 |
|
| 2018 |
Jia ZJ, Takayama H, Futamura Y, Aono H, Bauer JO, Strohmann C, Antonchick AP, Osada H, Waldmann H. Catalytic Enantioselective Synthesis of a Pyrrolizidine-Alkaloid-Inspired Compound Collection with Antiplasmodial Activity. The Journal of Organic Chemistry. PMID 29460633 DOI: 10.1021/Acs.Joc.7B03202 |
0.619 |
|
| 2018 |
Waldmann H, Jia ZJ, Shan G, Daniliuc CG, Antonchick AP. Enantioselective Synthesis of the Spiro-Tropanyl Oxindole Scaffold Through Bimetallic Relay Catalysis. Angewandte Chemie (International Ed. in English). PMID 29419912 DOI: 10.1002/Anie.201712882 |
0.646 |
|
| 2018 |
Murarka S, Antonchick A. Metal-Catalyzed Oxidative Coupling of Ketones and Ketone Enolates Synthesis. 50: 2150-2162. DOI: 10.1055/S-0037-1609715 |
0.767 |
|
| 2018 |
Matcha K, Antonchick AP. Transition-Metal-Free Radical Hydrotrifluoromethylation of Alkynes European Journal of Organic Chemistry. 2019: 309-312. DOI: 10.1002/Ejoc.201800291 |
0.376 |
|
| 2017 |
Waldmann H, Xu H, Laraia L, Schneider L, Louven K, Strohmann C, Antonchick AP. Highly Enantioselective Catalytic Vinylogous Propargylation of Coumarins Yields a Novel Autophagy Inhibitor Class. Angewandte Chemie (International Ed. in English). PMID 28696533 DOI: 10.1002/Anie.201706005 |
0.665 |
|
| 2017 |
Bering L, Manna S, Antonchick AP. Sustainable Oxidative Metal-Free Annulation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28564493 DOI: 10.1002/Chem.201702063 |
0.785 |
|
| 2017 |
Bering L, Antonchick AP. Selective transition-metal-free vicinal-dihydroxylation of saturated hydrocarbons. Chemical Science. 8: 452-457. PMID 28451192 DOI: 10.1039/C6Sc03055F |
0.536 |
|
| 2017 |
Manna S, Antonchick AP. Metal-Free Oxidative Dehydrogenative Diels-Alder Reaction for Selective Functionalization of Alkylbenzenes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28422331 DOI: 10.1002/Chem.201701535 |
0.783 |
|
| 2017 |
Waldmann H, Förster T, Lopéz-Tosco S, Ziegler S, Antonchick AP. Enantioselective Organocatalytic Synthesis of a Secoyohimbane-Inspired Compound Collection with Neuritogenic Activity. Chembiochem : a European Journal of Chemical Biology. PMID 28421720 DOI: 10.1002/Cbic.201700015 |
0.624 |
|
| 2017 |
Jia ZJ, Merten C, Gontla R, Daniliuc CG, Antonchick AP, Waldmann H. General Enantioselective C-H Activation with Efficiently Tunable Cyclopentadienyl Ligands. Angewandte Chemie (International Ed. in English). PMID 28124831 DOI: 10.1002/Anie.201611981 |
0.616 |
|
| 2017 |
Bering L, Manna S, Antonchick AP. Frontispiece: Sustainable, Oxidative, and Metal-Free Annulation Chemistry - a European Journal. 23. DOI: 10.1002/Chem.201784661 |
0.712 |
|
| 2016 |
Caporaso R, Manna S, Zinken S, Kochnev AR, Lukyanenko ER, Kurkin AV, Antonchick AP. Radical trideuteromethylation with deuterated dimethyl sulfoxide in the synthesis of heterocycles and labelled building blocks. Chemical Communications (Cambridge, England). 52: 12486-12489. PMID 27711354 DOI: 10.1039/C6Cc07196A |
0.753 |
|
| 2016 |
Xu H, Golz C, Strohmann C, Antonchick AP, Waldmann H. Enantiodivergent Combination of Natural Product Scaffolds Enabled by Catalytic Enantioselective Cycloaddition. Angewandte Chemie (International Ed. in English). PMID 27193834 DOI: 10.1002/Anie.201602084 |
0.65 |
|
| 2016 |
Song Z, Antonchick AP. Iridium(iii)-catalyzed regioselective C7-sulfonamidation of indoles. Organic & Biomolecular Chemistry. PMID 27173668 DOI: 10.1039/C6Ob00926C |
0.536 |
|
| 2016 |
Manna S, Antonchick AP. [1+1+1] Cyclotrimerization for the Synthesis of Cyclopropanes. Angewandte Chemie (International Ed. in English). 55: 5290-3. PMID 26997466 DOI: 10.1002/Anie.201600807 |
0.78 |
|
| 2016 |
Murarka S, Antonchick AP. Oxidative Heterocycle Formation Using Hypervalent Iodine(III) Reagents. Topics in Current Chemistry. 373: 75-104. PMID 26160138 DOI: 10.1007/128_2015_647 |
0.737 |
|
| 2016 |
Antonchick A, Waldmann H, Murarka S, Golz C, Strohmann C. Biology-Oriented Synthesis of 3,3-Spiro(2-tetrahydrofuranyl)oxindoles Synthesis. 49: 87-95. DOI: 10.1055/S-0035-1561665 |
0.79 |
|
| 2016 |
Song Z, Antonchick AP. Catching α-aminoalkyl radicals: cyclization between tertiary alkylanilines and alkenes Tetrahedron. 72: 7715-7721. DOI: 10.1016/J.Tet.2016.04.052 |
0.47 |
|
| 2015 |
Sellstedt M, Schwalfenberg M, Ziegler S, Antonchick AP, Waldmann H. Trienamine catalyzed asymmetric synthesis and biological investigation of a cytochalasin B-inspired compound collection. Organic & Biomolecular Chemistry. PMID 26606903 DOI: 10.1039/C5Ob02272J |
0.57 |
|
| 2015 |
Manna S, Serebrennikova PO, Utepova IA, Antonchick AP, Chupakhin ON. Hypervalent Iodine(III) in Direct Oxidative Amination of Arenes with Heteroaromatic Amines. Organic Letters. 17: 4588-91. PMID 26332538 DOI: 10.1021/Acs.Orglett.5B02320 |
0.778 |
|
| 2015 |
Manna S, Antonchick AP. Copper(I)-Catalyzed Radical Addition of Acetophenones to Alkynes in Furan Synthesis. Organic Letters. 17: 4300-3. PMID 26277912 DOI: 10.1021/Acs.Orglett.5B02114 |
0.784 |
|
| 2015 |
Narayan R, Matcha K, Antonchick AP. Metal-Free Oxidative CC Bond Formation through CH Bond Functionalization. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 14678-93. PMID 26239615 DOI: 10.1002/Chem.201502005 |
0.819 |
|
| 2015 |
Manna S, Antonchick AP. Copper-Catalyzed (2+1) Annulation of Acetophenones with Maleimides: Direct Synthesis of Cyclopropanes. Angewandte Chemie (International Ed. in English). 54: 14845-8. PMID 26094848 DOI: 10.1002/Anie.201502872 |
0.777 |
|
| 2015 |
Bering L, Antonchick AP. Regioselective Metal-Free Cross-Coupling of Quinoline N-Oxides with Boronic Acids. Organic Letters. 17: 3134-7. PMID 26066758 DOI: 10.1021/Acs.Orglett.5B01456 |
0.537 |
|
| 2015 |
Murarka S, Jia ZJ, Merten C, Daniliuc CG, Antonchick AP, Waldmann H. Rhodium(II)-Catalyzed Enantioselective Synthesis of Troponoids. Angewandte Chemie (International Ed. in English). 54: 7653-6. PMID 25959033 DOI: 10.1002/Anie.201502233 |
0.796 |
|
| 2015 |
Potowski M, Golz C, Strohmann C, Antonchick AP, Waldmann H. Biology-oriented synthesis of benzopyrano[3,4-c]pyrrolidines. Bioorganic & Medicinal Chemistry. 23: 2895-903. PMID 25792140 DOI: 10.1016/J.Bmc.2015.02.044 |
0.677 |
|
| 2015 |
Manna S, Narayan R, Golz C, Strohmann C, Antonchick AP. Regioselective annulation of nitrosopyridine with alkynes: straightforward synthesis of N-oxide-imidazopyridines. Chemical Communications (Cambridge, England). 51: 6119-22. PMID 25744096 DOI: 10.1039/C5Cc00533G |
0.805 |
|
| 2015 |
Potowski M, Merten C, Antonchick AP, Waldmann H. Catalytic aerobic oxidation and tandem enantioselective cycloaddition in cascade multicomponent synthesis. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 4913-7. PMID 25676025 DOI: 10.1002/Chem.201500125 |
0.663 |
|
| 2015 |
Samanta R, Narayan R, Bauer JO, Strohmann C, Sievers S, Antonchick AP. Oxidative regioselective amination of chromones exposes potent inhibitors of the hedgehog signaling pathway. Chemical Communications (Cambridge, England). 51: 925-8. PMID 25435304 DOI: 10.1039/C4Cc08376H |
0.798 |
|
| 2015 |
Jia ZJ, Daniliuc CG, Antonchick AP, Waldmann H. Phosphine-catalyzed dearomatizing [3+2] annulations of isoquinolinium methylides with allenes. Chemical Communications (Cambridge, England). 51: 1054-7. PMID 25434405 DOI: 10.1039/C4Cc08555H |
0.643 |
|
| 2015 |
Narayan R, Manna S, Antonchick AP. Hypervalent Iodine(III) in Direct Carbon-Hydrogen Bond Functionalization Synlett. 26: 1785-1803. DOI: 10.1055/S-0034-1379912 |
0.806 |
|
| 2015 |
Narayan R, Matcha K, Antonchick AP. ChemInform Abstract: Metal-Free Oxidative C-C Bond Formation Through C-H Bond Functionalization Cheminform. 46: no-no. DOI: 10.1002/CHIN.201550213 |
0.807 |
|
| 2015 |
Narayan R, Manna S, Antonchick AP. ChemInform Abstract: Hypervalent Iodine(III) in Direct Carbon-Hydrogen Bond Functionalization Cheminform. 46: no-no. DOI: 10.1002/CHIN.201542245 |
0.77 |
|
| 2015 |
Narayan R, Matcha K, Antonchick AP. Metal-Free Oxidative C-C Bond Formation through C-H Bond Functionalization Chemistry - a European Journal. DOI: 10.1002/chem.201502005 |
0.806 |
|
| 2014 |
Matcha K, Antonchick AP. Cascade multicomponent synthesis of indoles, pyrazoles, and pyridazinones by functionalization of alkenes. Angewandte Chemie (International Ed. in English). 53: 11960-4. PMID 25287788 DOI: 10.1002/Anie.201406464 |
0.523 |
|
| 2014 |
Manna S, Matcha K, Antonchick AP. Metal-free annulation of arenes with 2-aminopyridine derivatives: the methyl group as a traceless non-chelating directing group. Angewandte Chemie (International Ed. in English). 53: 8163-6. PMID 24938862 DOI: 10.1002/Anie.201403712 |
0.734 |
|
| 2014 |
Manna S, Antonchick AP. Organocatalytic oxidative annulation of benzamide derivatives with alkynes. Angewandte Chemie (International Ed. in English). 53: 7324-7. PMID 24849322 DOI: 10.1002/Anie.201404222 |
0.766 |
|
| 2014 |
Narayan R, Potowski M, Jia ZJ, Antonchick AP, Waldmann H. Catalytic enantioselective 1,3-dipolar cycloadditions of azomethine ylides for biology-oriented synthesis. Accounts of Chemical Research. 47: 1296-310. PMID 24730692 DOI: 10.1021/Ar400286B |
0.809 |
|
| 2014 |
Bruss H, Schuster H, Martinez R, Kaiser M, Antonchick AP, Waldmann H. Synthesis of the B-seco limonoid core scaffold. Beilstein Journal of Organic Chemistry. 10: 194-208. PMID 24605139 DOI: 10.3762/Bjoc.10.15 |
0.621 |
|
| 2014 |
Narayan R, Antonchick AP. Hypervalent iodine-mediated selective oxidative functionalization of (thio)chromones with alkanes. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 4568-72. PMID 24604840 DOI: 10.1002/Chem.201400186 |
0.822 |
|
| 2014 |
Matcha K, Antonchick AP. Mehrkomponentenkaskade zur Synthese von Indolen, Pyrazolen und Pyridazinonen durch Funktionalisierung von Alkenen Angewandte Chemie. 126: 12154-12158. DOI: 10.1002/Ange.201406464 |
0.358 |
|
| 2014 |
Manna S, Antonchick AP. Organokatalytische oxidative Anellierung von Benzamid‐Derivaten mit Alkinen Angewandte Chemie. 126: 7452-7455. DOI: 10.1002/Ange.201404222 |
0.699 |
|
| 2014 |
Manna S, Matcha K, Antonchick AP. Metallfreie Anellierung von Arenen mit 2-Aminopyridin-Derivaten: die Methylgruppe als spurlose nichtchelatisierende dirigierende Gruppe Angewandte Chemie. 126: 8302-8305. DOI: 10.1002/Ange.201403712 |
0.666 |
|
| 2013 |
Song Z, Samanta R, Antonchick AP. Rhodium(III)-catalyzed direct regioselective synthesis of 7-substituted indoles. Organic Letters. 15: 5662-5. PMID 24164341 DOI: 10.1021/Ol402626T |
0.756 |
|
| 2013 |
Narayan R, Bauer JO, Strohmann C, Antonchick AP, Waldmann H. Catalytic enantioselective synthesis of functionalized tropanes reveals novel inhibitors of hedgehog signaling. Angewandte Chemie (International Ed. in English). 52: 12892-6. PMID 24151037 DOI: 10.1002/Anie.201307392 |
0.809 |
|
| 2013 |
Takayama H, Jia ZJ, Kremer L, Bauer JO, Strohmann C, Ziegler S, Antonchick AP, Waldmann H. Discovery of inhibitors of the Wnt and Hedgehog signaling pathways through the catalytic enantioselective synthesis of an iridoid-inspired compound collection. Angewandte Chemie (International Ed. in English). 52: 12404-8. PMID 24115579 DOI: 10.1002/Anie.201306948 |
0.597 |
|
| 2013 |
Potowski M, Antonchick AP, Waldmann H. Catalytic asymmetric exo-selective [6+3] cycloaddition of iminoesters with fulvenes. Chemical Communications (Cambridge, England). 49: 7800-2. PMID 23884088 DOI: 10.1039/C3Cc43824D |
0.632 |
|
| 2013 |
Matcha K, Narayan R, Antonchick AP. Metal-free radical azidoarylation of alkenes: rapid access to oxindoles by cascade C-N and C-C bond-forming reactions. Angewandte Chemie (International Ed. in English). 52: 7985-9. PMID 23788465 DOI: 10.1002/Anie.201303550 |
0.804 |
|
| 2013 |
Antonchick AP, López-Tosco S, Parga J, Sievers S, Schürmann M, Preut H, Höing S, Schöler HR, Sterneckert J, Rauh D, Waldmann H. Highly enantioselective catalytic synthesis of neurite growth-promoting secoyohimbanes. Chemistry & Biology. 20: 500-9. PMID 23601639 DOI: 10.1016/J.Chembiol.2013.03.011 |
0.611 |
|
| 2013 |
Antonchick AP, Burgmann L. Direct selective oxidative cross-coupling of simple alkanes with heteroarenes. Angewandte Chemie (International Ed. in English). 52: 3267-71. PMID 23364911 DOI: 10.1002/Anie.201209584 |
0.419 |
|
| 2013 |
Matcha K, Antonchick AP. Metal-free cross-dehydrogenative coupling of heterocycles with aldehydes. Angewandte Chemie (International Ed. in English). 52: 2082-6. PMID 23307313 DOI: 10.1002/Anie.201208851 |
0.411 |
|
| 2013 |
Samanta R, Matcha K, Antonchick AP. Metal-free oxidative carbon-heteroatom bond formation through C-H bond functionalization European Journal of Organic Chemistry. 5769-5804. DOI: 10.1002/Ejoc.201300286 |
0.774 |
|
| 2013 |
Samanta R, Matcha K, Antonchick AP. ChemInform Abstract: Metal-Free Oxidative Carbon-Heteroatom Bond Formation Through C-H Bond Functionalization Cheminform. 44: no-no. DOI: 10.1002/CHIN.201348248 |
0.723 |
|
| 2013 |
Potowski M, Bauer JO, Strohmann C, Antonchick AP, Waldmann H. Corrigendum: Highly Enantioselective Catalytic [6+3] Cycloadditions of Azomethine Ylides Angewandte Chemie International Edition. 52: 7342-7342. DOI: 10.1002/Anie.201304263 |
0.629 |
|
| 2013 |
Potowski M, Bauer JO, Strohmann C, Antonchick AP, Waldmann H. Berichtigung: Highly Enantioselective Catalytic [6+3] Cycloadditions of Azomethine Ylides Angewandte Chemie. 125: 7484-7484. DOI: 10.1002/Ange.201304263 |
0.629 |
|
| 2013 |
Matcha K, Narayan R, Antonchick AP. Metallfreie radikalische Azidoarylierung von Alkenen: schneller Zugang zu Oxindolen durch kaskadenförmige C-N- und C-C-Bindungsbildung Angewandte Chemie. 125: 8143-8147. DOI: 10.1002/Ange.201303550 |
0.772 |
|
| 2012 |
Samanta R, Narayan R, Antonchick AP. Rhodium(III)-catalyzed direct oxidative cross coupling at the C5 position of chromones with alkenes. Organic Letters. 14: 6108-11. PMID 23190176 DOI: 10.1021/Ol303067F |
0.802 |
|
| 2012 |
Samanta R, Bauer JO, Strohmann C, Antonchick AP. Organocatalytic, oxidative, intermolecular amination and hydrazination of simple arenes at ambient temperature. Organic Letters. 14: 5518-21. PMID 23072473 DOI: 10.1021/Ol302607Y |
0.718 |
|
| 2012 |
Sos ML, Dietlein F, Peifer M, Schöttle J, Balke-Want H, Müller C, Koker M, Richters A, Heynck S, Malchers F, Heuckmann JM, Seidel D, Eyers PA, Ullrich RT, Antonchick AP, et al. A framework for identification of actionable cancer genome dependencies in small cell lung cancer. Proceedings of the National Academy of Sciences of the United States of America. 109: 17034-9. PMID 23035247 DOI: 10.1073/Pnas.1207310109 |
0.538 |
|
| 2012 |
Potowski M, Bauer JO, Strohmann C, Antonchick AP, Waldmann H. Highly enantioselective catalytic [6+3] cycloadditions of azomethine ylides. Angewandte Chemie (International Ed. in English). 51: 9512-6. PMID 22893358 DOI: 10.1002/Anie.201204394 |
0.629 |
|
| 2012 |
Potowski M, Schürmann M, Preut H, Antonchick AP, Waldmann H. Programmable enantioselective one-pot synthesis of molecules with eight stereocenters. Nature Chemical Biology. 8: 428-30. PMID 22426113 DOI: 10.1038/Nchembio.901 |
0.638 |
|
| 2012 |
Samanta R, Lategahn J, Antonchick AP. Metal-free direct oxidative intermolecular diarylation of anilides at ambient temperature assisted by cascade selective formation of C-C and C-N bonds. Chemical Communications (Cambridge, England). 48: 3194-6. PMID 22331064 DOI: 10.1039/C2Cc30324H |
0.751 |
|
| 2012 |
Samanta R, Kulikov K, Strohmann C, Antonchick AP. Metal-free electrocyclization at ambient temperature: Synthesis of 1-arylcarbazoles Synthesis (Germany). 44: 2325-2332. DOI: 10.1055/S-0032-1316743 |
0.726 |
|
| 2012 |
Samanta R, Antonchick AP. Metal-free oxidative C-H bond amination at ambient temperature Synlett. 23: 809-813. DOI: 10.1055/S-0031-1290531 |
0.755 |
|
| 2012 |
Samanta R, Kulikov K, Strohmann C, Antonchick AP. ChemInform Abstract: Metal-Free Electrocyclization at Ambient Temperature: Synthesis of 1-Arylcarbazoles. Cheminform. 43: no-no. DOI: 10.1002/chin.201246125 |
0.319 |
|
| 2012 |
Samanta R, Antonchick AP. ChemInform Abstract: Metal-Free Oxidative C-H Bond Amination at Ambient Temperature Cheminform. 43: no-no. DOI: 10.1002/CHIN.201224233 |
0.719 |
|
| 2012 |
Antonchick AP, Schuster H, Bruss H, Schuermann M, Preut H, Rauh D, Waldmann H. ChemInform Abstract: Enantioselective Synthesis of the Spirotryprostatin A Scaffold. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201217100 |
0.366 |
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| 2011 |
Rueping M, Theissmann T, Stoeckel M, Antonchick AP. Direct enantioselective access to 4-substituted tetrahydroquinolines by catalytic asymmetric transfer hydrogenation of quinolines. Organic & Biomolecular Chemistry. 9: 6844-50. PMID 21837348 DOI: 10.1039/C1Ob05870C |
0.62 |
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| 2011 |
Stöckigt J, Antonchick AP, Wu F, Waldmann H. The Pictet-Spengler reaction in nature and in organic chemistry. Angewandte Chemie (International Ed. in English). 50: 8538-64. PMID 21830283 DOI: 10.1002/Anie.201008071 |
0.618 |
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| 2011 |
Antonchick AP, Samanta R, Kulikov K, Lategahn J. Organocatalytic, oxidative, intramolecular C-H bond amination and metal-free cross-amination of unactivated arenes at ambient temperature. Angewandte Chemie (International Ed. in English). 50: 8605-8. PMID 21793137 DOI: 10.1002/Anie.201102984 |
0.748 |
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| 2011 |
Schuster H, Martinez R, Bruss H, Antonchick AP, Kaiser M, Schürmann M, Waldmann H. Synthesis of the B-seco limonoid scaffold. Chemical Communications (Cambridge, England). 47: 6545-7. PMID 21552600 DOI: 10.1039/C1Cc11388G |
0.579 |
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| 2011 |
Samanta R, Antonchick AP. Palladium-catalyzed double C-H activation directed by sulfoxides in the synthesis of dibenzothiophenes. Angewandte Chemie (International Ed. in English). 50: 5217-20. PMID 21506222 DOI: 10.1002/Anie.201100775 |
0.744 |
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| 2011 |
Antonchick AP, Schuster H, Bruss H, Schürmann M, Preut H, Rauh D, Waldmann H. Enantioselective synthesis of the spirotryprostatin A scaffold Tetrahedron. 67: 10195-10202. DOI: 10.1016/J.Tet.2011.04.056 |
0.631 |
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| 2011 |
Antonchick AP, Samanta R, Kulikov K, Lategahn J. Organokatalytische, oxidative, intramolekulare C-H-Bindungsaminierung und metallfreie Kreuzaminierung nichtaktivierter Arene bei Raumtemperatur Angewandte Chemie. 123: 8764-8767. DOI: 10.1002/Ange.201102984 |
0.72 |
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| 2011 |
Samanta R, Antonchick AP. Palladium-katalysierte, Sulfoxid-dirigierte doppelte C-H-Aktivierung zur Synthese von Dibenzothiophenen Angewandte Chemie. 123: 5323-5326. DOI: 10.1002/Ange.201100775 |
0.72 |
|
| 2011 |
Stöckigt J, Antonchick AP, Wu F, Waldmann H. Die Pictet-Spengler-Reaktion in der Natur und der organischen Chemie Angewandte Chemie. 123: 8692-8719. DOI: 10.1002/Ange.201008071 |
0.556 |
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| 2010 |
Rueping M, Brinkmann C, Antonchick AP, Atodiresei I. Asymmetric synthesis of indolines by catalytic enantioselective reduction of 3H-indoles. Organic Letters. 12: 4604-7. PMID 20857958 DOI: 10.1021/Ol1019234 |
0.636 |
|
| 2010 |
Antonchick AP, Gerding-Reimers C, Catarinella M, Schürmann M, Preut H, Ziegler S, Rauh D, Waldmann H. Highly enantioselective synthesis and cellular evaluation of spirooxindoles inspired by natural products. Nature Chemistry. 2: 735-40. PMID 20729892 DOI: 10.1038/Nchem.730 |
0.642 |
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| 2010 |
Waldmann H, Antonchick A, Gerding-Reimers C, Catarinella M, Schürmann M, Preut H, Ziegler S, Rauh D. Enantioselective Synthesis of Spirooxindoles Inspired by Natural Products Synfacts. 2010: 1379-1379. DOI: 10.1055/s-0030-1258906 |
0.581 |
|
| 2009 |
Vintonyak VV, Antonchick AP, Rauh D, Waldmann H. The therapeutic potential of phosphatase inhibitors Current Opinion in Chemical Biology. 13: 272-283. PMID 19410499 DOI: 10.1016/J.Cbpa.2009.03.021 |
0.547 |
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| 2009 |
Rueping M, Antonchick AP, Sugiono E, Grenader K. Asymmetric Brønsted acid catalysis: catalytic enantioselective synthesis of highly biologically active dihydroquinazolinones. Angewandte Chemie (International Ed. in English). 48: 908-10. PMID 19101974 DOI: 10.1002/Anie.200804770 |
0.596 |
|
| 2009 |
Rueping M, Antonchick A, Sugiono E, Grenader K. Asymmetrische Brønsted-Säure-Katalyse: katalytische enantioselektive Synthese von hochaktiven Dihydrochinazolinon-Wirkstoffen Angewandte Chemie. 121: 925-927. DOI: 10.1002/Ange.200804770 |
0.569 |
|
| 2008 |
Rueping M, Antonchick AP. Catalytic asymmetric aminoallylation of aldehydes: a catalytic enantioselective aza-Cope rearrangement. Angewandte Chemie (International Ed. in English). 47: 10090-3. PMID 19025749 DOI: 10.1002/Anie.200803610 |
0.592 |
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| 2008 |
Rueping M, Antonchick AP. A highly enantioselective Brønsted acid catalyzed reaction cascade. Angewandte Chemie (International Ed. in English). 47: 5836-8. PMID 18576441 DOI: 10.1002/Anie.200801435 |
0.596 |
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| 2008 |
Rueping M, Antonchick AP. Brønsted-acid-catalyzed activation of nitroalkanes: a direct enantioselective aza-Henry reaction. Organic Letters. 10: 1731-4. PMID 18393508 DOI: 10.1021/Ol8003589 |
0.598 |
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| 2008 |
Rueping M, Antonchick AP. ChemInform Abstract: Broensted-Acid-Catalyzed Activation of Nitroalkanes: A Direct Enantioselective Aza-Henry Reaction. Cheminform. 39. DOI: 10.1002/chin.200837075 |
0.547 |
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| 2008 |
Rueping M, Antonchick A. Katalytische asymmetrische Aminoallylierung von Aldehyden - eine katalytische enantioselektive Aza-Cope-Umlagerung Angewandte Chemie. 120: 10244-10247. DOI: 10.1002/Ange.200803610 |
0.514 |
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| 2008 |
Rueping M, Antonchick A. Eine hoch enantioselektive Brønsted‐Säure‐katalysierte Reaktionskaskade Angewandte Chemie. 120: 5920-5922. DOI: 10.1002/Ange.200801435 |
0.508 |
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| 2007 |
Rueping M, Antonchick AP, Brinkmann C. Dual catalysis: a combined enantioselective Brønsted acid and metal-catalyzed reaction--metal catalysis with chiral counterions. Angewandte Chemie (International Ed. in English). 46: 6903-6. PMID 17694520 DOI: 10.1002/Anie.200702439 |
0.592 |
|
| 2007 |
Rueping M, Antonchick AP. Organocatalytic enantioselective reduction of pyridines. Angewandte Chemie (International Ed. in English). 46: 4562-5. PMID 17492817 DOI: 10.1002/Anie.200701158 |
0.587 |
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| 2007 |
Rueping M, Ieawsuwan W, Antonchick AP, Nachtsheim BJ. Chiral Brønsted acids in the catalytic asymmetric Nazarov cyclization--the first enantioselective organocatalytic electrocyclic reaction. Angewandte Chemie (International Ed. in English). 46: 2097-100. PMID 17278163 DOI: 10.1002/Anie.200604809 |
0.604 |
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| 2007 |
Rueping M, Ieawsuwan W, Antonchick A, Nachtsheim B. Brønsted Acid Catalyzed Asymmetric Nazarov Cyclization Synfacts. 2007: 0432-0432. DOI: 10.1055/s-2007-968354 |
0.524 |
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| 2007 |
Rueping M, Antonchick A, Brinkmann C. Duale Katalyse: eine kombinierte enantioselektive Brønsted-Säure- und metallkatalysierte Reaktion – Metallkatalyse mit chiralem Gegenion Angewandte Chemie. 119: 7027-7030. DOI: 10.1002/Ange.200702439 |
0.489 |
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| 2007 |
Rueping M, Antonchick A. Organokatalytische enantioselektive Reduktion von Pyridinen Angewandte Chemie. 119: 4646-4649. DOI: 10.1002/Ange.200701158 |
0.484 |
|
| 2007 |
Rueping M, Ieawsuwan W, Antonchick A, Nachtsheim B. Chirale Brønsted-Säuren in der katalytischen asymmetrischen Nazarov-Reaktion – die erste enantioselektive organokatalytische elektrocyclische Reaktion Angewandte Chemie. 119: 2143-2146. DOI: 10.1002/Ange.200604809 |
0.527 |
|
| 2007 |
Rueping M, Sugiono E, Azap C, Theissmann T, Antonchick AP, Nawaz Khan S, Cho NJ, Kim HS. Imine Reduction and Reductive Amination Regio- and Stereo-Controlled Oxidations and Reductions. 5: 161-181. DOI: 10.1002/9780470090244.ch4 |
0.507 |
|
| 2006 |
Rueping M, Antonchick AP, Theissmann T. Remarkably low catalyst loading in Brønsted acid catalyzed transfer hydrogenations: enantioselective reduction of benzoxazines, benzothiazines, and benzoxazinones. Angewandte Chemie (International Ed. in English). 45: 6751-5. PMID 16986184 DOI: 10.1002/Anie.200601832 |
0.557 |
|
| 2006 |
Rueping M, Antonchick AP, Theissmann T. A highly enantioselective Brønsted acid catalyzed cascade reaction: organocatalytic transfer hydrogenation of quinolines and their application in the synthesis of alkaloids. Angewandte Chemie (International Ed. in English). 45: 3683-6. PMID 16639754 DOI: 10.1002/Anie.200600191 |
0.627 |
|
| 2006 |
Rueping M, Antonchick A, Theissmann T. Highly Enantioselective Organocatalytic Transfer Hydrogenation of Quinolines Synfacts. 2006: 0731-0731. DOI: 10.1055/s-2006-941911 |
0.501 |
|
| 2006 |
Rueping M, Theissmann T, Antonchick AP. Metal-free Brønsted acid catalyzed transfer hydrogenation - New organocatalytic reduction of quinolines Synlett. 1071-1074. DOI: 10.1055/S-2006-939706 |
0.619 |
|
| 2006 |
Rueping M, Theissmann T, Antonchick AP. Metal-Free Broensted Acid Catalyzed Transfer Hydrogenation — New Organocatalytic Reduction of Quinolines. Cheminform. 37. DOI: 10.1002/CHIN.200636141 |
0.338 |
|
| 2006 |
Rueping M, Antonchick AP, Theissmann T. Geringste Katalysatormengen in der Brønsted-Säure-katalysierten Transferhydrierung: enantioselektive Reduktion von Benzoxazinen, Benzthiazinen und Benzoxazinonen Angewandte Chemie. 118: 6903-6907. DOI: 10.1002/Ange.200601832 |
0.508 |
|
| 2006 |
Rueping M, Antonchick AP, Theissmann T. Eine hoch enantioselektive Brønsted-Säure-katalysierte Kaskadenreaktion: organokatalytische Transferhydrierung von Chinolinen und deren Anwendung in der Synthese von Alkaloiden Angewandte Chemie. 118: 3765-3768. DOI: 10.1002/Ange.200600191 |
0.552 |
|
| 2005 |
Khripach VA, Zhabinskii VN, Konstantinova OV, Khripach NB, Antonchick AV, Antonchick AP, Schneider B. Preparation of (25R)- and (25S)-26-functionalized steroids as tools for biosynthetic studies of cholic acids. Steroids. 70: 551-62. PMID 15894040 DOI: 10.1016/J.Steroids.2005.02.014 |
0.734 |
|
| 2005 |
Antonchick A, Svatos A, Schneider B, Konstantinova OV, Zhabinskii VN, Khripach VA. 2,3-Epoxybrassinosteroids are intermediates in the biosynthesis of castasterone in seedlings of Secale cereale. Phytochemistry. 66: 65-72. PMID 15649512 DOI: 10.1016/J.Phytochem.2004.11.008 |
0.683 |
|
| 2004 |
Antonchick AP, Schneider B, Zhabinskii VN, Khripach VA. Synthesis of [26,27-2H6]brassinosteroids from 23,24-bisnorcholenic acid methyl ester. Steroids. 69: 617-28. PMID 15465106 DOI: 10.1016/J.Steroids.2004.05.014 |
0.766 |
|
| 2004 |
Svatos A, Antonchick A, Schneider B. Determination of brassinosteroids in the sub-femtomolar range using dansyl-3-aminophenylboronate derivatization and electrospray mass spectrometry. Rapid Communications in Mass Spectrometry : Rcm. 18: 816-21. PMID 15052565 DOI: 10.1002/Rcm.1413 |
0.521 |
|
| 2003 |
Antonchick AP, Schneider B, Zhabinskii VN, Konstantinova OV, Khripach VA. Biosynthesis of 2,3-epoxybrassinosteroids in seedlings of Secale cereale. Phytochemistry. 63: 771-6. PMID 12877917 DOI: 10.1016/S0031-9422(03)00354-6 |
0.682 |
|
| 2002 |
Khripach VA, Zhabinskii VN, Antonchick AP, Konstantinova OV, Schneider B. Synthesis of hexadeuterated 23-dehydroxybrassinosteroids. Steroids. 67: 1101-8. PMID 12441196 DOI: 10.1016/S0039-128X(02)00071-5 |
0.764 |
|
| 2002 |
Khripach VA, Zhabinskii VN, Konstantinova OV, Khripach NB, Antonchick AP, Schneider B. [3,3]-Claisen rearrangements in 24alpha-methyl steroid synthesis. Application to campesterol, crinosterol, and Delta25-crinosterol side chain construction. Steroids. 67: 597-603. PMID 11996932 DOI: 10.1016/S0039-128X(02)00007-7 |
0.745 |
|
| 2002 |
Khripach VA, Zhabinskii VN, Konstantinova OV, Antonchick AP, Schneider B. Synthesis of [26-2H(3)]brassinosteroids. Steroids. 67: 587-95. PMID 11996931 DOI: 10.1016/S0039-128X(02)00004-1 |
0.732 |
|
| 2001 |
Konstantinova OV, Antonchick AP, Oldham NJ, Zhabinskii VN, Khripach VA, Schneider B. Analysis of underivatized brassinosteroids by HPLC/APCI-MS. Occurrence of 3-epibrassinolide in Arabidopsis thaliana Collection of Czechoslovak Chemical Communications. 66: 1729-1734. DOI: 10.1135/Cccc20011729 |
0.679 |
|
| 2001 |
Andres H, Sidorov G, Zverkov Y, Myasoedov N, Cimpoia A, Susan A, Saljoughian M, Morimoto H, Williams PG, Than C, Salter R, Moenius T, Ackermann P, Studer M, Morgan A, ... ... Antonchick AP, et al. 9thConference of the Central European Division e.V. of the International Isotope Society Journal of Labelled Compounds and Radiopharmaceuticals. 44: 947-985. DOI: 10.1002/Jlcr.527 |
0.673 |
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