Year |
Citation |
Score |
2020 |
Müller V, Ghorai D, Capdevila L, Messinis AM, Ribas X, Ackermann L. C-F Activation for C(sp)-C(sp) Cross-Coupling by a Secondary Phosphine Oxide (SPO)-Nickel Complex. Organic Letters. 22: 7034-7040. PMID 32816494 DOI: 10.1021/Acs.Orglett.0C02609 |
0.826 |
|
2020 |
Choi I, Müller V, Wang Y, Xue K, Kuniyil R, Karius V, Andreas LB, Alauzun JG, Ackermann L. Recyclable Ruthenium Catalyst for Distal meta-C-H Activation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32770682 DOI: 10.1002/Chem.202003622 |
0.753 |
|
2020 |
Wild M, Hahn F, Grau B, Herrmann L, Niesar A, Schütz M, Lorion MM, Ackermann L, Tsogoeva SB, Marschall M. The Artemisinin-Derived Autofluorescent Compound BG95 Exerts Strong Anticytomegaloviral Activity Based on a Mitochondrial Targeting Mechanism. International Journal of Molecular Sciences. 21. PMID 32759737 DOI: 10.3390/Ijms21155578 |
0.688 |
|
2020 |
Korvorapun K, Moselage M, Struwe J, Rogge T, Messinis A, Ackermann L. Regiodivergent C-H and C-C Alkylation by Ruthenium Catalysis: ortho versus meta Position-Selectivity. Angewandte Chemie (International Ed. in English). PMID 32700444 DOI: 10.1002/Anie.202007144 |
0.81 |
|
2020 |
Korvorapun K, Struwe J, Zangarelli A, Kuniyil R, Casnati A, Waeterschoot M, Ackermann L. Photo-Induced Ruthenium-Catalyzed C-H Arylation at Ambient Temperature. Angewandte Chemie. 59: 18103-18109. PMID 32662573 DOI: 10.1002/Anie.202003035 |
0.525 |
|
2020 |
Bu Q, Kuniyil R, Zhigao S, Gońka E, Ackermann L. Insights into Ruthenium(II/IV)-Catalyzed Distal C-H Oxygenation by Weak Coordination. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32596872 DOI: 10.1002/Chem.202003062 |
0.518 |
|
2020 |
Messinis AM, Finger LH, Hu L, Ackermann L. Allenes for Versatile Iron-Catalyzed C-H Activation by Weak O-Coordination: Mechanistic Insights by Kinetics, Intermediate Isolation and Computation. Journal of the American Chemical Society. PMID 32536163 DOI: 10.1021/Jacs.0C04837 |
0.459 |
|
2020 |
Çapcı A, Lorion MM, Mai C, Hahn F, Hodek J, Wangen C, Weber J, Marschall M, Ackermann L, Tsogoeva SB. (Iso)Quinoline-Artemisinin Hybrids via Click Chemistry: Highly Potent Agents against Viruses. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32485071 DOI: 10.1002/Chem.202001803 |
0.705 |
|
2020 |
Choi I, Messinis A, Ackermann L. C7-Indole Amidations and Alkenylations by Ruthenium(II) Catalysis. Angewandte Chemie (International Ed. in English). PMID 32485007 DOI: 10.1002/Anie.202006164 |
0.765 |
|
2020 |
Friis SD, Johansson MJ, Ackermann L. Cobalt-catalysed C-H methylation for late-stage drug diversification. Nature Chemistry. 12: 511-519. PMID 32472105 DOI: 10.1038/S41557-020-0475-7 |
0.411 |
|
2020 |
Gandeepan P, Finger LH, Meyer TH, Ackermann L. 3d metallaelectrocatalysis for resource economical syntheses. Chemical Society Reviews. 49: 4254-4272. PMID 32458919 DOI: 10.1039/D0Cs00149J |
0.339 |
|
2020 |
Zhang Y, Struwe J, Ackermann L. Rhodium-Catalyzed Electrooxidative C-H Olefination of Benzamides. Angewandte Chemie (International Ed. in English). PMID 32347643 DOI: 10.1002/Anie.202005257 |
0.547 |
|
2020 |
Ang NWJ, de Oliveira JCA, Ackermann L. Electro-Reductive Cobalt-Catalyzed Carboxylation: Cross-Electrophile Electro-coupling with Atmospheric CO2. Angewandte Chemie (International Ed. in English). PMID 32329560 DOI: 10.1002/Anie.202003218 |
0.341 |
|
2020 |
Zhang SK, Samanta RC, Del Vecchio A, Ackermann L. Evolution of High-Valent Nickelaelectro-Catalyzed C-H Activation: From Cross(-Electrophile)-Couplings to Electrooxidative C-H Transformations. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32329534 DOI: 10.1002/Chem.202001318 |
0.765 |
|
2020 |
Samanta RC, Struwe J, Ackermann L. Nickelaelectro-Catalyzed Mild C-H Alkylations at Room Temperature. Angewandte Chemie (International Ed. in English). PMID 32324948 DOI: 10.1002/Anie.202004958 |
0.523 |
|
2020 |
Tian C, Meyer TH, Stangier M, Dhawa U, Rauch K, Finger LH, Ackermann L. Cobaltaelectro-catalyzed C-H activation for resource-economical molecular syntheses. Nature Protocols. PMID 32296151 DOI: 10.1038/S41596-020-0306-8 |
0.823 |
|
2020 |
Dhawa U, Tian C, Wdowik T, Oliveira JCA, Hao J, Ackermann L. Enantioselective Palladaelectro-Catalyzed C-H Activations by Transient Directing Groups: Expedient Access to Helicenes. Angewandte Chemie (International Ed. in English). PMID 32243685 DOI: 10.1002/Anie.202003826 |
0.824 |
|
2020 |
da Silva Júnior EN, de Carvalho RL, Almeida RG, Rosa LG, Fantuzzi F, Rogge T, Costa PMS, Pessoa C, Jacob C, Ackermann L. Ruthenium(II)-Catalyzed Double Annulation of Quinones: Step-Economical Access to Valuable Bioactive Compounds. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32212283 DOI: 10.1002/Chem.202001434 |
0.789 |
|
2020 |
Meyer TH, de Oliveira JCA, Ghorai D, Ackermann L. Insights into Cobalta(III/IV/II)-Electrocatalysis: Oxidation-Induced Reductive Elimination for Twofold C-H Activation. Angewandte Chemie (International Ed. in English). PMID 32154625 DOI: 10.1002/Anie.202002258 |
0.856 |
|
2020 |
Yang L, Steinbock R, Scheremetjew A, Kuniyil R, Finger LH, Messinis AM, Ackermann L. Aza-Ruthena(II)-Bicyclo-[3.2.0]-Heptadiene: Key Intermediate for Ruthenaelectro(II/III/I)-Catalyzed Alkyne Annulations. Angewandte Chemie (International Ed. in English). PMID 32129528 DOI: 10.1002/Anie.202000762 |
0.476 |
|
2020 |
Mei R, Dhawa U, Samanta RC, Ma W, Wencel-Delord J, Ackermann L. Cobalt-Catalyzed Oxidative C-H Activation: Strategies and Concepts. Chemsuschem. PMID 32065843 DOI: 10.1002/Cssc.202000024 |
0.808 |
|
2020 |
Choi I, Müller V, Lole G, Köhler R, Karius V, Viöl W, Jooß C, Ackermann L. Photo-Induced Heterogeneous C-H Arylation by Reusable Hybrid-Copper Catalyst. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31943400 DOI: 10.1002/Chem.202000192 |
0.698 |
|
2020 |
Meyer TH, Chesnokov GA, Ackermann L. Cobaltaelectro-Catalyzed C-H Activation in Biomass-Derived Glycerol: Powered by Renewable Wind and Solar Energy. Chemsuschem. PMID 31917522 DOI: 10.1002/Cssc.202000057 |
0.479 |
|
2020 |
Mei R, Fang X, He L, Sun J, Zou L, Ma W, Ackermann L. Cobaltaelectro-catalyzed oxidative allene annulation by electro-removable hydrazides. Chemical Communications (Cambridge, England). PMID 31912810 DOI: 10.1039/C9Cc09076B |
0.531 |
|
2020 |
Ackermann L. Metalla-electrocatalyzed C-H Activation by Earth-Abundant 3d Metals and Beyond. Accounts of Chemical Research. 53: 84-104. PMID 31854967 DOI: 10.1021/Acs.Accounts.9B00510 |
0.443 |
|
2020 |
Weng Y, Ding X, Oliveira JCA, Xu X, Kaplaneris N, Zhu M, Chen H, Chen Z, Ackermann L. Peptide late-stage C(sp3)–H arylation by native asparagine assistance without exogenous directing groups Chemical Science. 11: 9290-9295. DOI: 10.1039/D0Sc03830J |
0.38 |
|
2020 |
Wu J, Kaplaneris N, Ni S, Kaltenhäuser F, Ackermann L. Late-stage C(sp2)–H and C(sp3)–H glycosylation of C-aryl/alkyl glycopeptides: mechanistic insights and fluorescence labeling Chemical Science. 11: 6521-6526. DOI: 10.1039/D0Sc01260B |
0.434 |
|
2020 |
Ma W, Kaplaneris N, Fang X, Gu L, Mei R, Ackermann L. Chelation-assisted transition metal-catalysed C–H chalcogenylations Organic Chemistry Frontiers. 7: 1022-1060. DOI: 10.1039/C9Qo01497G |
0.333 |
|
2020 |
Xu Z, Huang Z, Li Y, Kuniyil R, Zhang C, Ackermann L, Ruan Z. Catalyst-free, direct electrochemical synthesis of annulated medium-sized lactams through C–C bond cleavage Green Chemistry. 22: 1099-1104. DOI: 10.1039/C9Gc03901E |
0.387 |
|
2020 |
Zhu C, Kuniyil R, Jei BB, Ackermann L. Domino C–H Activation/Directing Group Migration/Alkyne Annulation: Unique Selectivity by d6-Cobalt(III) Catalysts Acs Catalysis. 10: 4444-4450. DOI: 10.1021/Acscatal.9B05413 |
0.386 |
|
2020 |
Korvorapun K, Kuniyil R, Ackermann L. Late-Stage Diversification by Selectivity Switch in meta-C–H Activation: Evidence for Singlet Stabilization Acs Catalysis. 10: 435-440. DOI: 10.1021/Acscatal.9B04592 |
0.353 |
|
2020 |
Dhawa U, Tian C, Li W, Ackermann L. Cobalta-Electrocatalyzed C–H Allylation with Unactivated Alkenes Acs Catalysis. 10: 6457-6462. DOI: 10.1021/Acscatal.0C01436 |
0.763 |
|
2020 |
Choi I, Messinis AM, Ackermann L. C7‐Indol‐Amidierung und ‐Alkenylierung durch Ruthenium(II)‐ Katalyse Angewandte Chemie. 132: 12635-12641. DOI: 10.1002/Ange.202006164 |
0.622 |
|
2020 |
Dhawa U, Tian C, Wdowik T, Oliveira JCA, Hao J, Ackermann L. Enantioselektive Pallada‐elektrokatalysierte C‐H‐Aktivierung durch transiente dirigierende Gruppen: Ein nützlicher Zugang zu Helicenen Angewandte Chemie. 132: 13553-13559. DOI: 10.1002/Ange.202003826 |
0.694 |
|
2020 |
Meyer TH, Oliveira JCA, Ghorai D, Ackermann L. Mechanistische Studien zu Cobalta(III/IV/II)‐Elektrokatalyse: Oxidativ‐induzierte reduktive Eliminierung zur zweifachen C‐H‐Aktivierung Angewandte Chemie. 132: 11048-11053. DOI: 10.1002/Ange.202002258 |
0.77 |
|
2019 |
Qiu Y, Scheremetjew A, Finger LH, Ackermann L. Electrophotocatalytic Undirected C-H Trifluoromethylations of (Het)Arenes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31875327 DOI: 10.1002/Chem.201905774 |
0.477 |
|
2019 |
Gońka E, Yang L, Steinbock R, Pesciaioli F, Kuniyil R, Ackermann L. π-Extended Polyaromatic Hydrocarbons by Sustainable Alkyne Annulations through Double C-H/N-H Activation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31820511 DOI: 10.1002/Chem.201905023 |
0.546 |
|
2019 |
Kong WJ, Shen Z, Finger LH, Ackermann L. Electrochemical Access to Aza-Polycyclic Aromatic Hydrocarbons: Rhodaelectro-Catalyzed Domino Annulations. Angewandte Chemie (International Ed. in English). PMID 31793169 DOI: 10.1002/Anie.201914775 |
0.541 |
|
2019 |
Massignan L, Tan X, Meyer TH, Kuniyil R, Messinis AM, Ackermann L. Electro-Catalyzed Hypervalent Iodine Orchestrated for Ruthenaelectro-Catalyzed C-H Oxygenation-. Angewandte Chemie (International Ed. in English). PMID 31777143 DOI: 10.1002/Anie.201914226 |
0.538 |
|
2019 |
Zhang SK, Struwe J, Hu L, Ackermann L. Nickellaelectro-Catalyzed C-H Alkoxylation with Secondary Alcohols: Oxidation-Induced Reductive Elimination at Nickel(III). Angewandte Chemie (International Ed. in English). PMID 31729814 DOI: 10.1002/Anie.201913930 |
0.448 |
|
2019 |
Zhu C, Stangier M, Oliveira JCA, Massignan L, Ackermann L. Iron-Electro-Catalyzed C-H Arylations: Mechanistic Insights Into Oxidation-Induced Reductive Elimination through Spectroscopy, CV, and Computation for Ferraelectrocatalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31658385 DOI: 10.1002/Chem.201904018 |
0.473 |
|
2019 |
Ellman JA, Ackermann L, Shi BF. The Breadth and Depth of C-H Functionalization. The Journal of Organic Chemistry. 84: 12701-12704. PMID 31623443 DOI: 10.1021/Acs.Joc.9B02663 |
0.482 |
|
2019 |
Kong WJ, Finger LH, Messinis AM, Kuniyil R, Oliveira JCA, Ackermann L. Flow Rhodaelectro-Catalyzed Alkyne Annulations by Versatile C-H Activation: Mechanistic Support for Rhodium(III/IV). Journal of the American Chemical Society. PMID 31549815 DOI: 10.1021/Jacs.9B07763 |
0.496 |
|
2019 |
Chen S, Chen W, Chen X, Chen G, Ackermann L, Tian X. Copper(I)-Catalyzed Oxyamination of β,γ-Unsaturated Hydrazones: Synthesis of Dihydropyrazoles. Organic Letters. PMID 31539265 DOI: 10.1021/Acs.Orglett.9B02733 |
0.316 |
|
2019 |
Rogge T, Ackermann L. Arene-Free Ruthenium(II/IV)-Catalyzed Bifurcated Arylation for Oxidative C-H/C-H Functionalizations. Angewandte Chemie. 58: 15640-15645. PMID 31476098 DOI: 10.1002/Anie.201909457 |
0.825 |
|
2019 |
Virelli M, Wang W, Kuniyil R, Wu J, Zanoni G, Fernandez A, Scott J, Vendrell M, Ackermann L. BODIPY-Labeled Cyclobutanes by Secondary C(sp3)─H Arylations for Live-Cell Imaging. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31433877 DOI: 10.1002/Chem.201903461 |
0.512 |
|
2019 |
Schischko A, Kaplaneris N, Rogge T, Sirvinskaite G, Son J, Ackermann L. Late-stage peptide C-H alkylation for bioorthogonal C-H activation featuring solid phase peptide synthesis. Nature Communications. 10: 3553. PMID 31391461 DOI: 10.1038/S41467-019-11395-3 |
0.831 |
|
2019 |
Mei R, Ma W, Zhang Y, Guo X, Ackermann L. Cobaltaelectro-Catalyzed Oxidative C-H/N-H Activation with 1,3-Diynes by Electro-Removable Hydrazides. Organic Letters. PMID 31365270 DOI: 10.1021/Acs.Orglett.9B02463 |
0.531 |
|
2019 |
da Silva Júnior EN, Jardim GAM, Jacob C, Dhawa U, Ackermann L, de Castro SL. Synthesis of quinones with highlighted biological applications: A critical update on the strategies towards bioactive compounds with emphasis on lapachones. European Journal of Medicinal Chemistry. 179: 863-915. PMID 31306817 DOI: 10.1016/J.Ejmech.2019.06.056 |
0.767 |
|
2019 |
Ferlin F, Yetra SR, Warratz S, Vaccaro L, Ackermann L. Reusable Pd@PEG Catalyst for Aerobic Dehydrogenative C-H/C-H Arylations of 1,2,3-Triazoles. Chemistry: a European Journal. 25: 11427-11431. PMID 31306515 DOI: 10.1002/Chem.201902901 |
0.543 |
|
2019 |
Boddie TE, Carpenter SH, Baker TM, DeMuth JC, Cera G, Brennessel WW, Ackermann L, Neidig ML. Identification and Reactivity of Cyclometalated Iron(II) Intermediates in Triazole-Directed Iron-Catalyzed C-H Activation. Journal of the American Chemical Society. PMID 31304750 DOI: 10.1021/Jacs.9B05269 |
0.733 |
|
2019 |
Çapcı A, Lorion MM, Wang H, Simon N, Leidenberger M, Silva MCB, Moreira DRM, Yongping Z, Yuqing M, Jia Yun C, Mun Lee Y, Friedrich O, Kappes B, Wang J, Ackermann L, et al. Artemisinin-(Iso)Quinoline Hybrids by C-H Activation and Click Chemistry: Combating Multidrug-Resistant Malaria. Angewandte Chemie (International Ed. in English). PMID 31290221 DOI: 10.1002/Anie.201907224 |
0.725 |
|
2019 |
Wang W, Subramanian P, Martinazzoli O, Wu J, Ackermann L. Glycopeptides by Linch-Pin C-H Activations for Peptide-Carbohydrate Conjugation by Manganese(I)-Catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31215694 DOI: 10.1002/Chem.201902788 |
0.802 |
|
2019 |
Mo J, Müller T, de Oliveira JCA, Demeshko S, Meyer F, Ackermann L. Iron-Catalyzed C-H Activation with Propargyl Acetates: Mechanistic Insights on Iron(II) by Experiment, Kinetics, Mössbauer Spectroscopy and Computation. Angewandte Chemie (International Ed. in English). PMID 31207070 DOI: 10.1002/Anie.201904110 |
0.494 |
|
2019 |
Han S, Liu S, Liu L, Ackermann L, Li J. Cobalt-Catalyzed Diastereoselective Difluoroalkylation/Giese Addition Domino Reactions. Organic Letters. PMID 31082243 DOI: 10.1021/Acs.Orglett.9B01400 |
0.393 |
|
2019 |
Loup J, Dhawa U, Pesciaioli F, Wencel‐Delord J, Ackermann L. Enantioselective C-H Activation with Earth-Abundant 3d Transition Metals. Angewandte Chemie. 58: 12803-12818. PMID 31077524 DOI: 10.1002/Anie.201904214 |
0.807 |
|
2019 |
Gandeepan P, Koeller J, Korvorapun K, Mohr J, Ackermann L. Visible-Light for Ruthenium-Catalyzed meta-C-H Alkylation at Room Temperature. Angewandte Chemie (International Ed. in English). PMID 31075177 DOI: 10.1002/Anie.201902258 |
0.506 |
|
2019 |
Long H, Xu K, Chen S, Lin J, Wu D, Wu B, Tian X, Ackermann L. Nickel-Catalyzed Intramolecular Direct Arylation of Imines toward Diverse Indoles. Organic Letters. PMID 30998370 DOI: 10.1021/Acs.Orglett.9B00600 |
0.401 |
|
2019 |
Santoro S, Ferlin F, Ackermann L, Vaccaro L. C-H functionalization reactions under flow conditions. Chemical Society Reviews. PMID 30942788 DOI: 10.1039/C8Cs00211H |
0.405 |
|
2019 |
Loup J, Parchomyk T, Lülf S, Demeshko S, Meyer F, Koszinowski K, Ackermann L. Mössbauer and mass spectrometry support for iron(ii) catalysts in enantioselective C-H activation. Dalton Transactions (Cambridge, England : 2003). PMID 30916099 DOI: 10.1039/C9Dt00705A |
0.443 |
|
2019 |
Sau SC, Mei R, Struwe J, Ackermann L. Cobaltaelectro-Catalyzed C-H Activation with Carbon Monoxide or Isocyanides. Chemsuschem. PMID 30897295 DOI: 10.1002/Cssc.201900378 |
0.531 |
|
2019 |
Chen P, Hao Y, Wang X, Yuan D, Yao Y, Ackermann L. Directing Group-free C7-alkylations of N-alkylindols Mediated by Cationic Zirconium Complexes: Role of Brønsted Acid for Catalytic Manifold. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30893504 DOI: 10.1002/Chem.201901268 |
0.416 |
|
2019 |
Yetra SR, Rogge T, Warratz S, Struwe J, Peng W, Vana P, Ackermann L. Micellar Catalysis for Ruthenium(II)-Catalyzed C-H Arylation: Weak-Coordination-Enabled C-H Activation in H2O. Angewandte Chemie (International Ed. in English). PMID 30860636 DOI: 10.1002/Anie.201901856 |
0.83 |
|
2019 |
Kong WJ, Finger LH, de Oliveira JCA, Ackermann L. Rhodaelectrocatalysis for Annulative C-H Activation: Polycyclic Aromatic Hydrocarbons by Versatile Double Electrocatalysis. Angewandte Chemie (International Ed. in English). PMID 30835907 DOI: 10.1002/Anie.201901565 |
0.511 |
|
2019 |
Zhu C, Kuniyil R, Ackermann L. Manganese(I)-Catalyzed C-H Activation/Diels-Alder/retro-Diels-Alder Domino Alkyne Annulation by Transformable Pyridines. Angewandte Chemie (International Ed. in English). PMID 30753749 DOI: 10.1002/Anie.201900495 |
0.552 |
|
2019 |
Ruan Z, Huang Z, Xu Z, Mo G, Tian X, Yu XY, Ackermann L. Catalyst-Free, Direct Electrochemical Tri- and Difluoroalkylation/Cyclization: Access to Functionalized Oxindoles and Quinolinones. Organic Letters. PMID 30730146 DOI: 10.1021/Acs.Orglett.9B00361 |
0.433 |
|
2019 |
Qiu Y, Scheremetjew A, Ackermann L. Electro-Oxidative C–C Alkenylation by Rhodium(III) Catalysis Journal of the American Chemical Society. 141: 2731-2738. PMID 30636408 DOI: 10.1021/Jacs.8B13692 |
0.386 |
|
2019 |
Shen Z, Huang H, Zhu C, Warratz S, Ackermann L. MnCl-Catalyzed C-H Alkylation on Azine Heterocycles. Organic Letters. PMID 30604972 DOI: 10.1021/Acs.Orglett.8B03924 |
0.557 |
|
2019 |
Ghorai D, Loup J, Zanoni G, Ackermann L. Air-Stable Secondary Phosphine Oxides for Nickel-Catalyzed Cross-Couplings of Aryl Ethers by C–O Activation Synlett. 30: 429-432. DOI: 10.1055/S-0037-1611663 |
0.326 |
|
2019 |
Koeller J, Gandeepan P, Ackermann L. Visible-Light-Induced Decarboxylative C–H Adamantylation of Azoles at Ambient Temperature Synthesis. 51: 1284-1292. DOI: 10.1055/S-0037-1611633 |
0.331 |
|
2019 |
Qiu Y, Struwe J, Ackermann L. Metallaelectro-Catalyzed C–H Activation by Weak Coordination Synlett. 30: 1164-1173. DOI: 10.1055/S-0037-1611568 |
0.376 |
|
2019 |
Gandeepan P, Kaplaneris N, Santoro S, Vaccaro L, Ackermann L. Biomass-Derived Solvents for Sustainable Transition Metal-Catalyzed C–H Activation Acs Sustainable Chemistry & Engineering. 7: 8023-8040. DOI: 10.1021/Acssuschemeng.9B00226 |
0.351 |
|
2019 |
Capdevila L, Meyer TH, Roldán-Gómez S, Luis JM, Ackermann L, Ribas X. Chemodivergent Nickel(0)-Catalyzed Arene C–F Activation with Alkynes: Unprecedented C–F/C–H Double Insertion Acs Catalysis. 9: 11074-11081. DOI: 10.1021/Acscatal.9B03620 |
0.401 |
|
2019 |
Jiang J, Liu H, Cao L, Zhao C, Liu Y, Ackermann L, Ke Z. Metallalkenyl, Metallacyclopropene, or Metallallylcarbenoid? Ru-Catalyzed Annulation between Benzoic Acid and Alkyne Acs Catalysis. 9: 9387-9392. DOI: 10.1021/Acscatal.9B02952 |
0.345 |
|
2019 |
Tian C, Dhawa U, Scheremetjew A, Ackermann L. Cupraelectro-Catalyzed Alkyne Annulation: Evidence for Distinct C–H Alkynylation and Decarboxylative C–H/C–C Manifolds Acs Catalysis. 9: 7690-7696. DOI: 10.1021/Acscatal.9B02348 |
0.764 |
|
2019 |
Dias GG, Nascimento TAd, Almeida AKAd, Bombaça ACS, Menna‐Barreto RFS, Jacob C, Warratz S, Júnior ENdS, Ackermann L. Ruthenium(II)‐Catalyzed C–H Alkenylation of Quinones: Diversity‐Oriented Strategy for Trypanocidal Compounds European Journal of Organic Chemistry. 2019: 2344-2353. DOI: 10.1002/Ejoc.201900004 |
0.33 |
|
2019 |
Tian C, Dhawa U, Struwe J, Ackermann L. Cobaltaelectro‐Catalyzed C—H Acyloxylation Chinese Journal of Chemistry. 37: 552-556. DOI: 10.1002/Cjoc.201900050 |
0.721 |
|
2019 |
Bechtoldt A, Ackermann L. Ruthenium(II)biscarboxylate‐Catalyzed Hydrogen‐Isotope Exchange by Alkene C−H Activation Chemcatchem. 11: 435-438. DOI: 10.1002/Cctc.201801601 |
0.329 |
|
2019 |
Çapcı A, Lorion MM, Wang H, Simon N, Leidenberger M, Borges Silva MC, Moreira DRM, Zhu Y, Meng Y, Chen JY, Lee YM, Friedrich O, Kappes B, Wang J, Ackermann L, et al. Inside Back Cover: Artemisinin–(Iso)quinoline Hybrids by C−H Activation and Click Chemistry: Combating Multidrug‐Resistant Malaria (Angew. Chem. Int. Ed. 37/2019) Angewandte Chemie International Edition. 58: 13161-13161. DOI: 10.1002/Anie.201910149 |
0.711 |
|
2019 |
Çapcı A, Lorion MM, Wang H, Simon N, Leidenberger M, Borges Silva MC, Moreira DRM, Zhu Y, Meng Y, Chen JY, Lee YM, Friedrich O, Kappes B, Wang J, Ackermann L, et al. Innenrücktitelbild: Artemisinin–(Iso)quinoline Hybrids by C−H Activation and Click Chemistry: Combating Multidrug‐Resistant Malaria (Angew. Chem. 37/2019) Angewandte Chemie. 131: 13295-13295. DOI: 10.1002/Ange.201910149 |
0.715 |
|
2019 |
Loup J, Dhawa U, Pesciaioli F, Wencel‐Delord J, Ackermann L. Enantioselektive C‐H‐Aktivierung mit natürlich vorkommenden 3d‐Übergangsmetallen Angewandte Chemie. 131: 12934-12949. DOI: 10.1002/Ange.201904214 |
0.689 |
|
2018 |
Kaplaneris N, Rogge T, Yin R, Wang H, Sirvinskaite G, Ackermann L. Late-Stage Diversification by Manganese-Catalyzed C-H Activation: Access to Acyclic, Hybrid and Stapled Peptides. Angewandte Chemie (International Ed. in English). PMID 30565829 DOI: 10.1002/Anie.201812705 |
0.807 |
|
2018 |
Bu Q, Gońka E, Kuciński K, Ackermann L. Cobalt-Catalyzed Hiyama-Type C-H Activation with Arylsiloxanes: Versatile Access to Highly ortho-Decorated Biaryls. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30537412 DOI: 10.1002/Chem.201806114 |
0.557 |
|
2018 |
Loup J, Müller V, Ghorai D, Ackermann L. Enantioselective Aluminum-Free Alkene Hydroarylations through C-H Activation by a Chiral Nickel/JoSPOphos Manifold. Angewandte Chemie (International Ed. in English). PMID 30517772 DOI: 10.1002/Anie.201813191 |
0.848 |
|
2018 |
Lorion MM, Kaplaneris N, Son J, Kuniyil R, Ackermann L. Late-Stage Peptide Diversification by Cobalt-Catalyzed C-H Activation: Sequential Multicatalysis for Stapled Peptides. Angewandte Chemie (International Ed. in English). PMID 30499607 DOI: 10.1002/Anie.201811668 |
0.821 |
|
2018 |
Gandeepan P, Müller T, Zell D, Cera G, Warratz S, Ackermann L. 3d Transition Metals for C-H Activation. Chemical Reviews. PMID 30480438 DOI: 10.1021/Acs.Chemrev.8B00507 |
0.743 |
|
2018 |
Zhang SK, Samanta RC, Sauermann N, Ackermann L. Nickel-Catalyzed Electrooxidative C-H Amination: Support for Nickel(IV). Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30379363 DOI: 10.1002/Chem.201805441 |
0.561 |
|
2018 |
Mei R, Koeller J, Ackermann L. Electrochemical ruthenium-catalyzed alkyne annulations by C-H/Het-H activation of aryl carbamates or phenols in protic media. Chemical Communications (Cambridge, England). PMID 30376023 DOI: 10.1039/C8Cc07732K |
0.551 |
|
2018 |
Dias GG, Rogge T, Kuniyil R, Jacob C, Menna-Barreto RFS, da Silva Júnior EN, Ackermann L. Ruthenium-catalyzed C-H oxygenation of quinones by weak O-coordination for potent trypanocidal agents. Chemical Communications (Cambridge, England). 54: 12840-12843. PMID 30374498 DOI: 10.1039/C8Cc07572G |
0.792 |
|
2018 |
Pesciaioli F, Dhawa U, Yin R, Oliveira JCA, John M, Ackermann L. Enantioselective Cobalt(III)-Catalyzed C-H Activation Enabled by Chiral Carboxylic Acid Cooperation. Angewandte Chemie (International Ed. in English). PMID 30289577 DOI: 10.1002/Anie.201808595 |
0.826 |
|
2018 |
Liang YF, Yang L, Rogge T, Ackermann L. Ruthenium(IV) Intermediates in C-H Activation/Annulation by Weak O-Coordination. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30251441 DOI: 10.1002/Chem.201804734 |
0.808 |
|
2018 |
Qiu Y, Stangier M, Meyer TH, Oliveira JCA, Ackermann L. Iridium-Catalyzed Electrooxidative C-H Activation by Chemo-Selective Redox-Catalyst Cooperation. Angewandte Chemie (International Ed. in English). PMID 30199130 DOI: 10.1002/Anie.201809611 |
0.568 |
|
2018 |
Yetra SR, Shen Z, Wang H, Ackermann L. Thiocarbonyl-enabled ferrocene C-H nitrogenation by cobalt(III) catalysis: thermal and mechanochemical. Beilstein Journal of Organic Chemistry. 14: 1546-1553. PMID 30013681 DOI: 10.3762/Bjoc.14.131 |
0.553 |
|
2018 |
Detmar E, Müller V, Zell D, Ackermann L, Breugst M. Cobalt-catalyzed C-H cyanations: Insights into the reaction mechanism and the role of London dispersion. Beilstein Journal of Organic Chemistry. 14: 1537-1545. PMID 30013680 DOI: 10.3762/Bjoc.14.130 |
0.512 |
|
2018 |
Wang W, Lorion M, Shah J, Kapdi AR, Ackermann L. Late-Stage Peptide Diversification by Position-Selective C-H Activation. Angewandte Chemie (International Ed. in English). PMID 29969532 DOI: 10.1002/Anie.201806250 |
0.786 |
|
2018 |
Sauermann N, Meyer TH, Ackermann L. Electrochemical Cobalt-Catalyzed C-H Activation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29920808 DOI: 10.1002/Chem.201802706 |
0.546 |
|
2018 |
Qiu Y, Struwe J, Meyer TH, Oliveira JCACA, Ackermann L. Catalyst- and Reagent-free Electrochemical Azole C-H Amination. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29901828 DOI: 10.1002/Chem.201802832 |
0.539 |
|
2018 |
Fang Y, Rogge T, Ackermann L, Wang SY, Ji SJ. Nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides. Nature Communications. 9: 2240. PMID 29884782 DOI: 10.1038/S41467-018-04646-2 |
0.767 |
|
2018 |
Wang W, Lorion M, Martinazzoli O, Ackermann L. BODIPY Peptide Labeling by Late-Stage C(sp3)-H Activation. Angewandte Chemie (International Ed. in English). PMID 29883018 DOI: 10.1002/Anie.201804654 |
0.788 |
|
2018 |
Liang YF, Steinbock R, Yang L, Ackermann L. Continuous Visible Light-Photo-Flow for Manganese-Catalyzed (Het)Arene C-H Arylation. Angewandte Chemie (International Ed. in English). PMID 29882633 DOI: 10.1002/Anie.201805644 |
0.438 |
|
2018 |
da Silva Júnior EN, Jardim GAM, Gomes RS, Liang YF, Ackermann L. Weakly-coordinating N-oxide and carbonyl groups for metal-catalyzed C-H activation: the case of A-ring functionalization. Chemical Communications (Cambridge, England). PMID 29863215 DOI: 10.1039/C8Cc03147A |
0.481 |
|
2018 |
Mei R, Sauermann N, Oliveira JCA, Ackermann L. Electro-Removable Traceless Hydrazides for Cobalt-Catalyzed Electro-Oxidative C-H/N-H Activation with Internal Alkynes. Journal of the American Chemical Society. PMID 29812927 DOI: 10.1021/Jacs.8B03521 |
0.549 |
|
2018 |
Kalepu J, Gandeepan P, Ackermann L, Pilarski LT. C4-H indole functionalisation: precedent and prospects. Chemical Science. 9: 4203-4216. PMID 29780550 DOI: 10.1039/C7Sc05336C |
0.526 |
|
2018 |
Mo J, Müller T, Oliveira JCA, Ackermann L. 1,4-Iron Migration for Expedient Allene Annulations through Iron-Catalyzed C-H/N-H/C-O/C-H Functionalizations. Angewandte Chemie (International Ed. in English). PMID 29697898 DOI: 10.1002/Anie.201801324 |
0.499 |
|
2018 |
Santoro S, Marrocchi A, Lanari D, Ackermann L, Vaccaro L. Towards Sustainable C-H Functionalization Reactions: The Emerging Role of Bio-Based Reaction Media. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29667710 DOI: 10.1002/Chem.201801114 |
0.49 |
|
2018 |
Qiu Y, Kong W, Struwe J, Sauermann N, Rogge T, Scheremetjew A, Ackermann L. Electrooxidative Rhodium-Catalyzed C-H/C-H Activation: Electricity as Oxidant for Cross-Dehydrogenative Alkenylation. Angewandte Chemie. 57: 5828-5832. PMID 29633454 DOI: 10.1002/Anie.201803342 |
0.811 |
|
2018 |
Qiu Y, Tian C, Massignan L, Rogge T, Ackermann L. Electrooxidative Ruthenium-Catalyzed C-H/O-H Annulation by Weak O-Coordination. Angewandte Chemie (International Ed. in English). PMID 29603565 DOI: 10.1002/Anie.201802748 |
0.814 |
|
2018 |
Sauermann N, Mei R, Ackermann L. Electrochemical C-H Amination by Cobalt Catalysis in a Renewable Solvent. Angewandte Chemie (International Ed. in English). PMID 29509336 DOI: 10.1002/Anie.201802206 |
0.536 |
|
2018 |
Liang YF, Steinbock R, Münch A, Stalke D, Ackermann L. Manganese-Catalyzed Carbonylative Annulations for Redox-Neutral Late-Stage Diversification. Angewandte Chemie (International Ed. in English). PMID 29474755 DOI: 10.1002/Anie.201801111 |
0.351 |
|
2018 |
Fumagalli F, Warratz S, Zhang SK, Rogge T, Zhu C, Stückl AC, Ackermann L. Arene-Ligand-free Ruthenium(II/III) Manifold for meta-C-H Alkylation: Remote Purine Diversification. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29406613 DOI: 10.1002/Chem.201800530 |
0.824 |
|
2018 |
Tian C, Massignan L, Meyer TH, Ackermann L. Electrochemical C-H/N-H Activation by Water-Tolerant Cobalt-Catalysis at Room Temperature. Angewandte Chemie (International Ed. in English). PMID 29316187 DOI: 10.1002/Anie.201712647 |
0.488 |
|
2018 |
Ackermann L, Dinca M, Glorius F, Hisatomi T, Kinjo R, Kubota J, Kudo A, Studer A, Tang B, Winkler J. Outstanding Reviewers for: Chemical Science in 2017 Chemical Science. 9. DOI: 10.1039/C8Sc90078G |
0.385 |
|
2018 |
Ferlin F, Luciani L, Santoro S, Marrocchi A, Lanari D, Bechtoldt A, Ackermann L, Vaccaro L. A continuous flow approach for the C–H functionalization of 1,2,3-triazoles in γ-valerolactone as a biomass-derived medium Green Chemistry. 20: 2888-2893. DOI: 10.1039/C8Gc01115J |
0.349 |
|
2018 |
Bechtoldt A, Baumert ME, Vaccaro L, Ackermann L. Ruthenium(II) oxidase catalysis for C–H alkenylations in biomass-derived γ-valerolactone Green Chemistry. 20: 398-402. DOI: 10.1039/C7Gc03353B |
0.371 |
|
2018 |
Ghorai D, Finger LH, Zanoni G, Ackermann L. Bimetallic Nickel Complexes for Aniline C–H Alkylations Acs Catalysis. 8: 11657-11662. DOI: 10.1021/Acscatal.8B03770 |
0.798 |
|
2018 |
Meyer TH, Oliveira JCA, Sau SC, Ang NWJ, Ackermann L. Electrooxidative Allene Annulations by Mild Cobalt-Catalyzed C–H Activation Acs Catalysis. 8: 9140-9147. DOI: 10.1021/Acscatal.8B03066 |
0.378 |
|
2018 |
Sauermann N, Meyer TH, Qiu Y, Ackermann L. Electrocatalytic C–H Activation Acs Catalysis. 8: 7086-7103. DOI: 10.1021/Acscatal.8B01682 |
0.445 |
|
2018 |
Zhu C, Oliveira JCA, Shen Z, Huang H, Ackermann L. Manganese(II/III/I)-Catalyzed C–H Arylations in Continuous Flow Acs Catalysis. 8: 4402-4407. DOI: 10.1021/Acscatal.8B00166 |
0.395 |
|
2018 |
Korvorapun K, Kaplaneris N, Rogge T, Warratz S, Stückl AC, Ackermann L. Sequential meta-/ortho-C–H Functionalizations by One-Pot Ruthenium(II/III) Catalysis Acs Catalysis. 886-892. DOI: 10.1021/Acscatal.7B03648 |
0.399 |
|
2018 |
Dhawa U, Zell D, Yin R, Okumura S, Murakami M, Ackermann L. C–H/C–F functionalization by E-selective ruthenium (II) catalysis Journal of Catalysis. 364: 14-18. DOI: 10.1016/J.Jcat.2018.04.019 |
0.734 |
|
2018 |
Tang M, Li Y, Han S, Liu L, Ackermann L, Li J. Rhodium(III)-Catalyzed C-H Alkylation/Nucleophilic Addition Domino Reaction European Journal of Organic Chemistry. 2019: 660-664. DOI: 10.1002/Ejoc.201801535 |
0.535 |
|
2018 |
Liang Y, Massignan L, Ackermann L. Sustainable Manganese‐Catalyzed C−H Activation/Hydroarylation of Imines Chemcatchem. 10: 2768-2772. DOI: 10.1002/Cctc.201800144 |
0.352 |
|
2018 |
Wang W, Lorion MM, Shah J, Kapdi AR, Ackermann L. Peptid-Diversifizierung durch positionsselektive C-H-Aktivierung im späten Synthesestadium Angewandte Chemie. 130: 14912-14930. DOI: 10.1002/Ange.201806250 |
0.774 |
|
2018 |
Ma W, Weng Z, Rogge T, Gu L, Lin J, Peng A, Luo X, Gou X, Ackermann L. Ruthenium(II)‐Catalyzed C−H Chalcogenation of Anilides Advanced Synthesis & Catalysis. 360: 704-710. DOI: 10.1002/Adsc.201701147 |
0.382 |
|
2017 |
Sauermann N, Meyer T, Tian C, Ackermann L. Electrochemical Cobalt-Catalyzed C-H Oxygenation at Room Temperature. Journal of the American Chemical Society. PMID 29149561 DOI: 10.1021/Jacs.7B11025 |
0.519 |
|
2017 |
Bu Q, Rogge T, Kotek V, Ackermann L. Distal Weak Coordination of Acetamides in Ruthenium(II)-Catalyzed C-H Activation Processes. Angewandte Chemie (International Ed. in English). PMID 29141119 DOI: 10.1002/Anie.201711108 |
0.825 |
|
2017 |
Bauer M, Wang W, Lorion ML, Dong C, Ackermann L. Internal Peptide Late-Stage Diversification: Peptide Isosteric Triazoles for Primary and Secondary C(sp3)-H Activation. Angewandte Chemie (International Ed. in English). PMID 29135064 DOI: 10.1002/Anie.201710136 |
0.46 |
|
2017 |
Nakanowatari S, Müller T, Oliveira JCA, Ackermann L. Bifurcated Nickel-Catalyzed Functionalizations: Heteroarene C-H Activation with Allenes. Angewandte Chemie (International Ed. in English). PMID 29065240 DOI: 10.1002/Anie.201709087 |
0.573 |
|
2017 |
Lorion MM, Maindan K, Kapdi AR, Ackermann L. Heteromultimetallic catalysis for sustainable organic syntheses. Chemical Society Reviews. 46: 7399-7420. PMID 29051927 DOI: 10.1039/C6Cs00787B |
0.761 |
|
2017 |
Wang H, Pesciaioli F, Oliveira JCA, Warratz S, Ackermann L. Synergistic Manganese(I) C-H Activation Catalysis in Continuous Flow: Chemo-Selective Hydroarylation. Angewandte Chemie (International Ed. in English). PMID 28985452 DOI: 10.1002/Anie.201708271 |
0.509 |
|
2017 |
Loup J, Zell D, Oliveira JCA, Keil H, Stalke D, Ackermann L. Asymmetric Iron-Catalyzed C-H Alkylation Enabled by Remote Ligand meta-Substitution. Angewandte Chemie (International Ed. in English). 56: 14197-14201. PMID 28922549 DOI: 10.1002/Anie.201709075 |
0.508 |
|
2017 |
Kumar P, Rogge T, Yetra SR, Bechtholdt A, Clot E, Ackermann L. Mild Decarboxylative C-H Alkylation: Computational Insights for Solvent-Robust Ruthenium(II) Domino Manifold. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28901047 DOI: 10.1002/Chem.201703680 |
0.822 |
|
2017 |
Huang H, Nakanowatari S, Ackermann L. Selectivity Control in Ruthenium(II)-Catalyzed C-H/N-O Activation with Alkynyl Bromides. Organic Letters. 19: 4620-4623. PMID 28809574 DOI: 10.1021/Acs.Orglett.7B02247 |
0.472 |
|
2017 |
Ruan Z, Ghorai D, Zanoni G, Ackermann L. Nickel-catalyzed C-H activation of purine bases with alkyl halides. Chemical Communications (Cambridge, England). PMID 28759075 DOI: 10.1039/C7Cc05011A |
0.836 |
|
2017 |
Liu W, Cera G, Oliveira JCA, Shen Z, Ackermann L. MnCl2-Catalyzed C-H Alkylations with Alkyl Halides. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28704583 DOI: 10.1002/Chem.201703191 |
0.792 |
|
2017 |
Shen Z, Cera G, Haven T, Ackermann L. Tri-Substituted Triazole-Enabled C-H Activation of Benzyl and Aryl Amines by Iron Catalysis. Organic Letters. PMID 28686458 DOI: 10.1021/Acs.Orglett.7B01672 |
0.768 |
|
2017 |
Zell D, Müller V, Dhawa U, Bursch M, Presa R, Grimme S, Ackermann L. Mild Cobalt(III)-Catalyzed Allylative C-F/C-H Functionalizations at Room Temperature. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28675487 DOI: 10.1002/Chem.201702528 |
0.806 |
|
2017 |
Zell D, Bursch M, Müller V, Grimme S, Ackermann L. Switch of C-H Activation Mechanism for Full Selectivity Control in Cobalt(III)-Catalyzed C-H Alkylations. Angewandte Chemie (International Ed. in English). PMID 28636265 DOI: 10.1002/Anie.201704196 |
0.53 |
|
2017 |
Liang YF, Müller V, Liu W, Münch A, Stalke D, Ackermann L. Methylenecyclopropane Annulation by Manganese(I)-Catalyzed Stereoselective C-H/C-C Activation. Angewandte Chemie (International Ed. in English). PMID 28605110 DOI: 10.1002/Anie.201704767 |
0.551 |
|
2017 |
Li J, Korvorapun K, De Sarkar S, Rogge T, Burns DJ, Warratz S, Ackermann L. Ruthenium(II)-catalysed remote C-H alkylations as a versatile platform to meta-decorated arenes. Nature Communications. 8: 15430. PMID 28598411 DOI: 10.1038/Ncomms15430 |
0.851 |
|
2017 |
Zhang Z, Han S, Tang M, Ackermann L, Li J. C-H Alkylations of (Hetero)Arenes by Maleimides and Maleate Esters through Cobalt(III) Catalysis. Organic Letters. PMID 28590740 DOI: 10.1021/Acs.Orglett.7B01480 |
0.558 |
|
2017 |
Cera G, Haven T, Ackermann L. Iron-catalyzed C-H/N-H activation by triazole guidance: versatile alkyne annulation. Chemical Communications. 53: 6460-6463. PMID 28561113 DOI: 10.1039/C7Cc03376A |
0.464 |
|
2017 |
Mei R, Zhang SK, Ackermann L. Ruthenium(II)-Catalyzed C-H Alkynylation of Weakly Coordinating Benzoic Acids. Organic Letters. PMID 28558248 DOI: 10.1021/Acs.Orglett.7B01294 |
0.535 |
|
2017 |
Gandeepan P, Mo J, Ackermann L. Photo-induced copper-catalyzed C-H chalcogenation of azoles at room temperature. Chemical Communications (Cambridge, England). PMID 28513650 DOI: 10.1039/C7Cc03107F |
0.482 |
|
2017 |
Wang H, Lorion MM, Ackermann L. Air-Stable Manganese(I)-Catalyzed C-H Activation for Decarboxylative C-H/C-O Cleavages in Water. Angewandte Chemie (International Ed. in English). PMID 28474796 DOI: 10.1002/Anie.201702193 |
0.804 |
|
2017 |
Moselage M, Li J, Kramm F, Ackermann L. Ruthenium(II)-Catalyzed C-C Arylations and Alkylations: Decarbamoylative C-C Functionalizations. Angewandte Chemie (International Ed. in English). PMID 28378513 DOI: 10.1002/Anie.201701231 |
0.46 |
|
2017 |
Meyer TH, Liu W, Feldt M, Wuttke A, Mata RA, Ackermann L. Manganese(I)-Catalyzed Dispersion-Enabled C-H/C-C Activation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28317205 DOI: 10.1002/Chem.201701191 |
0.524 |
|
2017 |
Raghuvanshi K, Zell D, Ackermann L. Ruthenium(II)-Catalyzed C–H Oxygenations of Reusable Sulfoximine Benzamides Organic Letters. 19: 1278-1281. PMID 28234011 DOI: 10.1021/Acs.Orglett.6B03898 |
0.404 |
|
2017 |
Ruan Z, Sauermann N, Manoni E, Ackermann L. Manganese-Catalyzed C-H Alkynylation: Expedient Peptide Synthesis and Modification. Angewandte Chemie (International Ed. in English). PMID 28181732 DOI: 10.1002/Anie.201611118 |
0.513 |
|
2017 |
Cera G, Haven T, Ackermann L. Iron-Catalyzed C-H Alkynylation through Triazole Assistance: Expedient Access to Bioactive Heterocycles. Chemistry (Weinheim An Der Bergstrasse, Germany). 23: 3577-3582. PMID 28177547 DOI: 10.1002/Chem.201700587 |
0.751 |
|
2017 |
Ruan Z, Zhang SK, Zhu C, Ruth PN, Stalke D, Ackermann L. Ruthenium(II)-Catalyzed meta C-H Mono- and Difluoromethylations by Phosphine/Carboxylate Cooperation. Angewandte Chemie (International Ed. in English). PMID 28106316 DOI: 10.1002/Anie.201611595 |
0.554 |
|
2017 |
Schischko A, Ren H, Kaplaneris N, Ackermann L. Bioorthogonal Diversification of Peptides through Selective Ruthenium(II)-Catalyzed C-H Activation. Angewandte Chemie (International Ed. in English). PMID 28074503 DOI: 10.1002/Anie.201609631 |
0.482 |
|
2017 |
Warratz S, Burns DJ, Zhu C, Korvorapun K, Rogge T, Scholz J, Jooss C, Gelman D, Ackermann L. meta-C-H Bromination on Purine Bases by Heterogeneous Ruthenium Catalysis. Angewandte Chemie (International Ed. in English). PMID 28044396 DOI: 10.1002/Anie.201609014 |
0.822 |
|
2017 |
Mei R, Zhang S, Ackermann L. Concise Synthesis of Lamellarin Alkaloids by C–H/N–H Activation: Evaluation of Metal Catalysts in Oxidative Alkyne Annulation Synlett. 28: 1715-1718. DOI: 10.1055/S-0036-1591209 |
0.434 |
|
2017 |
Sauermann N, Loup J, Kootz D, Yatham V, Berkessel A, Ackermann L. Triazolylidene Ligands Allow Cobalt-Catalyzed C–H/C–O Alkenylations at Ambient Temperature Synthesis. 49: 3476-3484. DOI: 10.1055/S-0036-1590471 |
0.376 |
|
2017 |
Ma W, Gandeepan P, Li J, Ackermann L. Recent advances in positional-selective alkenylations: removable guidance for twofold C–H activation Organic Chemistry Frontiers. 4: 1435-1467. DOI: 10.1039/C7Qo00134G |
0.351 |
|
2017 |
Ferlin F, Santoro S, Ackermann L, Vaccaro L. Heterogeneous C–H alkenylations in continuous-flow: oxidative palladium-catalysis in a biomass-derived reaction medium Green Chemistry. 19: 2510-2514. DOI: 10.1039/C7Gc01103B |
0.402 |
|
2017 |
Santoro S, Ferlin F, Luciani L, Ackermann L, Vaccaro L. Biomass-derived solvents as effective media for cross-coupling reactions and C–H functionalization processes Green Chemistry. 19: 1601-1612. DOI: 10.1039/C7Gc00067G |
0.352 |
|
2017 |
Zell D, Dhawa U, Müller V, Bursch M, Grimme S, Ackermann L. C–F/C–H Functionalization by Manganese(I) Catalysis: Expedient (Per)Fluoro-Allylations and Alkenylations Acs Catalysis. 7: 4209-4213. DOI: 10.1021/Acscatal.7B01208 |
0.751 |
|
2017 |
Wang H, Lorion MM, Ackermann L. Domino C–H/N–H Allylations of Imidates by Cobalt Catalysis Acs Catalysis. 7: 3430-3433. DOI: 10.1021/Acscatal.7B00756 |
0.768 |
|
2017 |
Nakanowatari S, Mei R, Feldt M, Ackermann L. Cobalt(III)-Catalyzed Hydroarylation of Allenes via C–H Activation Acs Catalysis. 7: 2511-2515. DOI: 10.1021/Acscatal.7B00207 |
0.409 |
|
2017 |
Gandeepan P, Koeller J, Ackermann L. Expedient C–H Chalcogenation of Indolines and Indoles by Positional-Selective Copper Catalysis Acs Catalysis. 7: 1030-1034. DOI: 10.1021/Acscatal.6B03236 |
0.434 |
|
2017 |
Gandeepan P, Ackermann L. Transient Directing Groups for Transformative C–H Activation by Synergistic Metal Catalysis Chem. 4: 199-222. DOI: 10.1016/J.Chempr.2017.11.002 |
0.369 |
|
2017 |
Zell D, Bursch M, Müller V, Grimme S, Ackermann L. Switch of C−H Activation Mechanism for Full Selectivity Control in Cobalt(III)-Catalyzed C−H Alkylations Angewandte Chemie. DOI: 10.1002/Ange.201704196 |
0.342 |
|
2017 |
Ghorai D, Müller V, Keil H, Stalke D, Zanoni G, Tkachenko BA, Schreiner PR, Ackermann L. Cover Picture: Secondary Phosphine Oxide Preligands for Palladium-Catalyzed C-H (Hetero)Arylations: Efficient Access to Pybox Ligands (Adv. Synth. Catal. 18/2017) Advanced Synthesis & Catalysis. 359: 3078-3078. DOI: 10.1002/Adsc.201701122 |
0.516 |
|
2017 |
Ghorai D, Müller V, Keil H, Stalke D, Zanoni G, Tkachenko BA, Schreiner PR, Ackermann L. Secondary Phosphine Oxide Preligands for Palladium-Catalyzed C-H (Hetero)Arylations: Efficient Access to Pybox Ligands Advanced Synthesis & Catalysis. 359: 3137-3141. DOI: 10.1002/Adsc.201700663 |
0.49 |
|
2017 |
Ma W, Dong H, Wang D, Ackermann L. Late‐Stage Diversification of Non‐Steroidal Anti‐Inflammatory Drugs by Transition Metal‐Catalyzed C–H Alkenylations, Thiolations and Selenylations Advanced Synthesis & Catalysis. 359: 966-973. DOI: 10.1002/Adsc.201600937 |
0.303 |
|
2016 |
Zhang Z, Tang M, Han S, Ackermann L, Li J. Carboxylate-Enhanced Rhodium(III)-Catalyzed Aryl C-H Alkylation with Conjugated Alkenes under Mild Conditions. The Journal of Organic Chemistry. PMID 27966963 DOI: 10.1021/Acs.Joc.6B02672 |
0.499 |
|
2016 |
Liu W, Richter SC, Mei R, Feldt M, Ackermann L. Synergistic Heterobimetallic Manifold for Expedient Manganese(I)-Catalyzed C-H Cyanation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27786397 DOI: 10.1002/Chem.201604621 |
0.557 |
|
2016 |
De Sarkar S, Kumar NY, Ackermann L. Ruthenium(II)Biscarboxylate Catalyzed Borylations of C(sp2)-H and C(sp3)-H Bonds. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27779339 DOI: 10.1002/Chem.201604943 |
0.525 |
|
2016 |
Mei R, Zhu C, Ackermann L. Ruthenium(ii)-catalyzed C-H functionalizations on benzoic acids with aryl, alkenyl and alkynyl halides by weak-O-coordination. Chemical Communications (Cambridge, England). PMID 27768150 DOI: 10.1039/C6Cc07773K |
0.55 |
|
2016 |
Cera G, Ackermann L. Iron-Catalyzed C-H Functionalization Processes. Topics in Current Chemistry (Cham). 374: 57. PMID 27573499 DOI: 10.1007/S41061-016-0059-6 |
0.754 |
|
2016 |
Liang YF, Massignan L, Liu W, Ackermann L. Catalyst-Guided C=Het Hydroarylations via Manganese-Catalyzed Additive-Free C-H Activation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27556882 DOI: 10.1002/Chem.201603848 |
0.465 |
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2016 |
Wang H, Lorion MM, Ackermann L. Overcoming the Limitations of C-H Activation with Strongly Coordinating N-Heterocycles by Cobalt Catalysis. Angewandte Chemie (International Ed. in English). PMID 27440498 DOI: 10.1002/Anie.201603260 |
0.821 |
|
2016 |
Tian X, Yang F, Rasina D, Bauer M, Warratz S, Ferlin F, Vaccaro L, Ackermann L. C-H arylations of 1,2,3-triazoles by reusable heterogeneous palladium catalysts in biomass-derived γ-valerolactone. Chemical Communications (Cambridge, England). PMID 27419251 DOI: 10.1039/C6Cc03468C |
0.534 |
|
2016 |
Li J, Tang M, Zang L, Zhang X, Zhang Z, Ackermann L. Amidines for Versatile Cobalt(III)-Catalyzed Synthesis of Isoquinolines through C-H Functionalization with Diazo Compounds. Organic Letters. PMID 27219713 DOI: 10.1021/Acs.Orglett.6B01199 |
0.532 |
|
2016 |
Zell D, Bu Q, Feldt M, Ackermann L. Mild C-H/C-C Activation by Z-Selective Cobalt Catalysis. Angewandte Chemie (International Ed. in English). PMID 27145065 DOI: 10.1002/Anie.201601778 |
0.523 |
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2016 |
Cera G, Ackermann L. Weak O-Assistance Outcompeting Strong N,N-Bidentate Directing Groups in Copper-Catalyzed C-H Chalcogenation. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 8475-8. PMID 27124082 DOI: 10.1002/Chem.201601821 |
0.756 |
|
2016 |
Liu W, Richter SC, Zhang Y, Ackermann L. Manganese(I)-Catalyzed Substitutive C-H Allylation. Angewandte Chemie (International Ed. in English). PMID 27095021 DOI: 10.1002/Anie.201601560 |
0.539 |
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2016 |
Kumar NYP, Bechtoldt A, Raghuvanshi K, Ackermann L. Ruthenium(II)‐Catalyzed Decarboxylative C−H Activation: Versatile Routes to meta‐Alkenylated Arenes Angewandte Chemie. 55: 6929-6932. PMID 26996920 DOI: 10.1002/Anie.201600490 |
0.377 |
|
2016 |
Mei R, Wang H, Warratz S, Macgregor SA, Ackermann L. Cobalt-Catalyzed Oxidase C-H/N-H Alkyne Annulation: Mechanistic Insights and Access to anti-Cancer Agents. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26992149 DOI: 10.1002/Chem.201601101 |
0.519 |
|
2016 |
Yang F, Koeller J, Ackermann L. Photoinduced Copper-Catalyzed C-H Arylation at Room Temperature. Angewandte Chemie (International Ed. in English). PMID 26961222 DOI: 10.1002/Anie.201512027 |
0.426 |
|
2016 |
Borie C, Ackermann L, Nechab M. Enantioselective syntheses of indanes: from organocatalysis to C–H functionalization Chemical Society Reviews. 45: 1368-1386. PMID 26728953 DOI: 10.1039/C5Cs00622H |
0.341 |
|
2016 |
Cera G, Haven T, Ackermann L. Expedient Iron-Catalyzed C-H Allylation/Alkylation by Triazole Assistance with Ample Scope. Angewandte Chemie (International Ed. in English). 55: 1484-8. PMID 26663680 DOI: 10.1002/Anie.201509603 |
0.777 |
|
2016 |
Bechtoldt A, Tirler C, Raghuvanshi K, Warratz S, Kornhaaß C, Ackermann L. Ruthenium Oxidase Catalysis for Site‐Selective C–H Alkenylations with Ambient O2 as the Sole Oxidant Angewandte Chemie. 55: 264-267. PMID 26489871 DOI: 10.1002/Anie.201507801 |
0.393 |
|
2016 |
Tonin MDL, Zell D, Müller V, Ackermann L. Ruthenium(II)-Catalyzed C−H Methylation with Trifluoroborates Synthesis. 49: 127-134. DOI: 10.1055/S-0036-1588890 |
0.343 |
|
2016 |
Santoro S, Kozhushkov SI, Ackermann L, Vaccaro L. Heterogeneous catalytic approaches in C–H activation reactions Green Chemistry. 18: 3471-3493. DOI: 10.1039/C6Gc00385K |
0.376 |
|
2016 |
Fenner S, Ackermann L. C–H carboxylation of heteroarenes with ambient CO2 Green Chemistry. 18: 3804-3807. DOI: 10.1039/C6Gc00200E |
0.322 |
|
2016 |
Ruan Z, Lackner S, Ackermann L. Nickel-Catalyzed C–H Alkynylation of Anilines: Expedient Access to Functionalized Indoles and Purine Nucleobases Acs Catalysis. 6: 4690-4693. DOI: 10.1021/Acscatal.6B01120 |
0.404 |
|
2016 |
Liu W, Ackermann L. Manganese-Catalyzed C–H Activation Acs Catalysis. 6: 3743-3752. DOI: 10.1021/Acscatal.6B00993 |
0.367 |
|
2016 |
Raghuvanshi K, Zell D, Rauch K, Ackermann L. Ketone-Assisted Ruthenium(II)-Catalyzed C–H Imidation: Access to Primary Aminoketones by Weak Coordination Acs Catalysis. 6: 3172-3175. DOI: 10.1021/Acscatal.6B00711 |
0.399 |
|
2016 |
Wang H, Moselage M, González MJ, Ackermann L. Selective Synthesis of Indoles by Cobalt(III)-Catalyzed C–H/N–O Functionalization with Nitrones Acs Catalysis. 6: 2705-2709. DOI: 10.1021/Acscatal.5B02937 |
0.4 |
|
2016 |
Mei R, Loup J, Ackermann L. Oxazolinyl-Assisted C-H Amidation by Cobalt(III) Catalysis Acs Catalysis. 6: 793-797. DOI: 10.1021/Acscatal.5B02661 |
0.568 |
|
2016 |
Moselage M, Li J, Ackermann L. Cobalt-Catalyzed C―H Activation Acs Catalysis. 6: 230-263. DOI: 10.1021/Acscatal.5B02344 |
0.393 |
|
2016 |
Santrač D, Cella S, Wang W, Ackermann L. Palladium‐Catalyzed C–H Arylation of Amides by Triazole Assistance European Journal of Organic Chemistry. 2016: 5429-5436. DOI: 10.1002/Ejoc.201601045 |
0.359 |
|
2016 |
Hubrich J, Ackermann L. Amino Acid Ligands for Ruthenium(II)‐Catalyzed C–H Arylation of Aryltetrazoles with Chlorides: Expedient Access to Antihypertension Drugs European Journal of Organic Chemistry. 2016: 3700-3704. DOI: 10.1002/Ejoc.201600742 |
0.406 |
|
2016 |
Ruan Z, Lackner S, Ackermann L. A General Strategy for the Nickel-Catalyzed C-H Alkylation of Anilines Angewandte Chemie - International Edition. 55: 3153-3157. DOI: 10.1002/Anie.201510743 |
0.572 |
|
2016 |
Mei R, Ackermann L. Front Cover Picture: Cobalt-Catalyzed C−H Functionalizations by Imidate Assistance with Aryl and Alkyl Chlorides (Adv. Synth. Catal. 15/2016) Advanced Synthesis and Catalysis. 358: 2361. DOI: 10.1002/Adsc.201600800 |
0.38 |
|
2016 |
Mei R, Ackermann L. Cobalt-Catalyzed C−H Functionalizations by Imidate Assistance with Aryl and Alkyl Chlorides Advanced Synthesis and Catalysis. 358: 2443-2448. DOI: 10.1002/Adsc.201600384 |
0.426 |
|
2016 |
Wang L, Rauch K, Lygin AV, Kozhushkov SI, Ackermann L. Ruthenium-Catalyzed Direct Oxidative Alkenylation of Arenes Through Twofold CH Bond Functionalization in Water: Synthesis of Ethyl (E)-3-(2-Acetamido-4-Methylphenyl)Acrylate Organic Syntheses. 131-147. DOI: 10.1002/0471264229.Os092.10 |
0.317 |
|
2015 |
Zell D, Warratz S, Gelman D, Alchemy S, Ackermann L. Single-Component Phosphinous Acid Ruthenium(II) Catalysts for Versatile C-H Activations by Metal-Ligand Cooperation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26639161 DOI: 10.1002/Chem.201504851 |
0.539 |
|
2015 |
Sauermann N, González MJ, Ackermann L. Cobalt(III)-Catalyzed C-H Alkynylation with Bromoalkynes under Mild Conditions. Organic Letters. 17: 5316-9. PMID 26492592 DOI: 10.1021/Acs.Orglett.5B02678 |
0.451 |
|
2015 |
Wang H, Koeller J, Liu W, Ackermann L. Cobalt(III)-Catalyzed CH/NO Functionalizations: Isohypsic Access to Isoquinolines. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26420729 DOI: 10.1002/Chem.201503624 |
0.324 |
|
2015 |
Li J, Warratz S, Zell D, De Sarkar S, Ishikawa EE, Ackermann L. N-Acyl Amino Acid Ligands for Ruthenium(II)-catalyzed meta-C-H tert-Alkylation with Removable Auxiliaries. Journal of the American Chemical Society. PMID 26418891 DOI: 10.1021/Jacs.5B08435 |
0.769 |
|
2015 |
Liu W, Bang J, Zhang Y, Ackermann L. Manganese(I)-Catalyzed C-H Aminocarbonylation of Heteroarenes. Angewandte Chemie (International Ed. in English). PMID 26418747 DOI: 10.1002/Anie.201507087 |
0.497 |
|
2015 |
Nakanowatari S, Ackermann L. Ruthenium(II)‐Catalyzed C ? H Functionalizations with Allenes: Versatile Allenylations and Allylations Chemistry: a European Journal. 21: 16246-16251. PMID 26376731 DOI: 10.1002/Chem.201502785 |
0.571 |
|
2015 |
Ackermann L, Li J. C-H activation: Following directions. Nature Chemistry. 7: 686-687. PMID 26291937 DOI: 10.1038/Nchem.2334 |
0.479 |
|
2015 |
Zhu Y, Bauer M, Ackermann L. Late-Stage Peptide Diversification by Bioorthogonal Catalytic CH Arylation at 23 °C in H2 O. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 9980-3. PMID 26037620 DOI: 10.1002/Chem.201501831 |
0.385 |
|
2015 |
Li J, Ackermann L. Cobalt(III)-Catalyzed Aryl and Alkenyl C-H Aminocarbonylation with Isocyanates and Acyl Azides. Angewandte Chemie. 54: 8551-8554. PMID 25969403 DOI: 10.1002/Anie.201501926 |
0.576 |
|
2015 |
Graczyk K, Haven T, Ackermann L. Iron‐Catalyzed C(sp2) ? H and C(sp3) ? H Methylations of Amides and Anilides Chemistry: a European Journal. 21: 8812-8815. PMID 25950870 DOI: 10.1002/Chem.201501134 |
0.403 |
|
2015 |
Moselage M, Sauermann N, Richter SC, Ackermann L. C-H alkenylations with alkenyl acetates, phosphates, carbonates, and carbamates by cobalt catalysis at 23 °C. Angewandte Chemie (International Ed. in English). 54: 6352-5. PMID 25864965 DOI: 10.1002/Anie.201412319 |
0.502 |
|
2015 |
Warratz S, Kornhaaß C, Cajaraville A, Niepötter B, Stalke D, Ackermann L. Ruthenium(II)-catalyzed C-H activation/alkyne annulation by weak coordination with O2 as the sole oxidant. Angewandte Chemie (International Ed. in English). 54: 5513-7. PMID 25737001 DOI: 10.1002/Anie.201500600 |
0.422 |
|
2015 |
Li J, Ackermann L. Cobalt‐Catalyzed C ? H Arylations with Weakly‐Coordinating Amides and Tetrazoles: Expedient Route to Angiotensin‐II‐Receptor Blockers Chemistry: a European Journal. 21: 5718-5722. PMID 25728566 DOI: 10.1002/Chem.201500552 |
0.565 |
|
2015 |
Liu W, Zell D, John M, Ackermann L. Manganese-catalyzed synthesis of cis-β-amino acid esters through organometallic C-H activation of ketimines. Angewandte Chemie (International Ed. in English). 54: 4092-6. PMID 25663350 DOI: 10.1002/Anie.201411808 |
0.385 |
|
2015 |
Raghuvanshi K, Rauch K, Ackermann L. Ruthenium(II)‐Catalyzed C ? H Acyloxylation of Phenols with Removable Auxiliary Chemistry: a European Journal. 21: 1790-1794. PMID 25431040 DOI: 10.1002/Chem.201405071 |
0.577 |
|
2015 |
Li J, Ackermann L. Cobalt‐Catalyzed CH Cyanation of Arenes and Heteroarenes Angewandte Chemie. 54: 3635-3638. PMID 25404422 DOI: 10.1002/Anie.201409247 |
0.351 |
|
2015 |
Moselage M, Sauermann N, Koeller J, Liu W, Gelman D, Ackermann L. Cobalt(III)-Catalyzed Allylation with Allyl Acetates by C-H/C-O Cleavage Synlett. 26: 1596-1600. DOI: 10.1055/S-0034-1379927 |
0.526 |
|
2015 |
Li J, Ackermann L. Carboxylate-assisted ruthenium(II)-catalyzed C–H activations of monodentate amides with conjugated alkenes Organic Chemistry Frontiers. 2: 1035-1039. DOI: 10.1039/C5Qo00167F |
0.416 |
|
2015 |
Ackermann L. Robust Ruthenium(II)-Catalyzed C–H Arylations: Carboxylate Assistance for the Efficient Synthesis of Angiotensin-II-Receptor Blockers Organic Process Research & Development. 19: 260-269. DOI: 10.1021/Op500330G |
0.392 |
|
2015 |
Hubrich J, Himmler T, Rodefeld L, Ackermann L. Ruthenium(II)-Catalyzed C–H Arylation of Azoarenes by Carboxylate Assistance Acs Catalysis. 5: 4089-4093. DOI: 10.1021/Acscatal.5B00939 |
0.423 |
|
2015 |
Ma W, Ackermann L. Cobalt(II)-Catalyzed Oxidative C–H Alkenylations: Regio- and Site-Selective Access to Isoindolin-1-one Acs Catalysis. 5: 2822-2825. DOI: 10.1021/Acscatal.5B00322 |
0.386 |
|
2015 |
Tirler C, Ackermann L. Ruthenium(II)-catalyzed cross-dehydrogenative C–H alkenylations by triazole assistance Tetrahedron. 71: 4543-4551. DOI: 10.1016/J.Tet.2015.02.033 |
0.405 |
|
2015 |
Li J, Ackermann L. Cobalt(III)-katalysierte C-H-Aminocarbonylierung von Arenen und Alkenen mit Isocyanaten und Acylaziden† Angewandte Chemie. 127: 8671-8674. DOI: 10.1002/Ange.201501926 |
0.513 |
|
2015 |
Warratz S, Kornhaaß C, Cajaraville A, Niepötter B, Stalke D, Ackermann L. Ruthenium(II)-katalysierte C-H-Aktivierung/Alkinanellierung durch schwache Koordination mit O2als einzigem Oxidationsmittel Angewandte Chemie. 127: 5604-5608. DOI: 10.1002/Ange.201500600 |
0.496 |
|
2015 |
Moselage M, Sauermann N, Richter SC, Ackermann L. C-H-Alkenylierungen mit Alkenylacetaten, -phosphaten, -carbonaten und -carbamaten durch Cobalt-Katalyse bei 23 °C Angewandte Chemie. 127: 6450-6453. DOI: 10.1002/Ange.201412319 |
0.46 |
|
2015 |
Liu W, Zell D, John M, Ackermann L. Mangankatalysierte Synthese von cis‐β‐Aminosäureestern mittels metallorganischer C‐H‐Aktivierung von Ketiminen Angewandte Chemie. 127: 4165-4169. DOI: 10.1002/Ange.201411808 |
0.428 |
|
2015 |
Musa S, Ghosh A, Vaccaro L, Ackermann L, Gelman D. EfficientE-Selective Transfer Semihydrogenation of Alkynes by Means of Ligand-Metal Cooperating Ruthenium Catalyst Advanced Synthesis & Catalysis. 357: 2351-2357. DOI: 10.1002/Adsc.201500372 |
0.386 |
|
2014 |
Yang F, Ackermann L. Dehydrative C–H/N–OH Functionalizations in H2O by Ruthenium(II) Catalysis: Subtle Effect of Carboxylate Ligands and Mechanistic Insight Journal of Organic Chemistry. 79: 12070-12082. PMID 25335189 DOI: 10.1021/Jo501884V |
0.416 |
|
2014 |
Ma W, Mei R, Tenti G, Ackermann L. Ruthenium(II)-catalyzed oxidative C-H alkenylations of sulfonic acids, sulfonyl chlorides and sulfonamides. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 15248-51. PMID 25283954 DOI: 10.1002/Chem.201404604 |
0.544 |
|
2014 |
De Sarkar S, Ackermann L. Ruthenium(II)-catalyzed C-H activation with isocyanates: a versatile route to phthalimides. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 13932-6. PMID 25201510 DOI: 10.1002/Chem.201404261 |
0.801 |
|
2014 |
Zhu Y, Bauer M, Ploog J, Ackermann L. Late-stage diversification of peptides by metal-free C-H arylation. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 13099-102. PMID 25168602 DOI: 10.1002/Chem.201404603 |
0.479 |
|
2014 |
Yang F, Rauch K, Kettelhoit K, Ackermann L. Aldehyde-assisted ruthenium(II)-catalyzed C-H oxygenations. Angewandte Chemie. 53: 11285-11288. PMID 25154310 DOI: 10.1002/Anie.201405647 |
0.38 |
|
2014 |
Ackermann L. Cobalt-Catalyzed C–H Arylations, Benzylations, and Alkylations with Organic Electrophiles and Beyond Journal of Organic Chemistry. 79: 8948-8954. PMID 25102352 DOI: 10.1021/Jo501361K |
0.406 |
|
2014 |
Mamari HHA, Diers E, Ackermann L. Triazole‐Assisted Ruthenium‐Catalyzed C ? H Arylation of Aromatic Amides Chemistry: a European Journal. 20: 9739-9743. PMID 24957002 DOI: 10.1002/Chem.201403019 |
0.504 |
|
2014 |
Li J, John M, Ackermann L. Amidines for versatile ruthenium(II)-catalyzed oxidative C-H activations with internal alkynes and acrylates. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 5403-8. PMID 24677682 DOI: 10.1002/Chem.201304944 |
0.555 |
|
2014 |
Nakanowatari S, Ackermann L. Ruthenium(II)‐Catalyzed Synthesis of Isochromenes by C ? H Activation with Weakly Coordinating Aliphatic Hydroxyl Groups Chemistry: a European Journal. 20: 5409-5413. PMID 24677395 DOI: 10.1002/Chem.201400161 |
0.546 |
|
2014 |
Schinkel M, Wang L, Bielefeld K, Ackermann L. Ruthenium(II)-Catalyzed C(sp3)–H α-Alkylation of Pyrrolidines Organic Letters. 16: 1876-1879. PMID 24635222 DOI: 10.1021/Ol500300W |
0.46 |
|
2014 |
Gu Q, Al Mamari HH, Graczyk K, Diers E, Ackermann L. Iron-catalyzed C(sp(2))-H and C(sp(3))-H arylation by triazole assistance. Angewandte Chemie (International Ed. in English). 53: 3868-71. PMID 24596034 DOI: 10.1002/Anie.201311024 |
0.469 |
|
2014 |
Song W, Lackner S, Ackermann L. Nickel‐Catalyzed CH Alkylations: Direct Secondary Alkylations and Trifluoroethylations of Arenes Angewandte Chemie. 53: 2477-2480. PMID 24482119 DOI: 10.1002/Anie.201309584 |
0.302 |
|
2014 |
Liu W, Ackermann L. Versatile ruthenium(II)-catalyzed C-H cyanations of benzamides. Chemical Communications (Cambridge, England). 50: 1878-81. PMID 24402371 DOI: 10.1039/C3Cc49502G |
0.531 |
|
2014 |
Masarwa A, Didier D, Zabrodski T, Schinkel M, Ackermann L, Marek I. Merging allylic carbon-hydrogen and selective carbon-carbon bond activation. Nature. 505: 199-203. PMID 24317692 DOI: 10.1038/Nature12761 |
0.448 |
|
2014 |
Wang L, Ackermann L. Ruthenium-catalyzed ortho-C???H halogenations of benzamides Chemical Communications. 50: 1083-1085. PMID 24317223 DOI: 10.1039/C3Cc47852A |
0.447 |
|
2014 |
Thirunavukkarasu VS, Kozhushkov SI, Ackermann L. C-H nitrogenation and oxygenation by ruthenium catalysis. Chemical Communications (Cambridge, England). 50: 29-39. PMID 24212194 DOI: 10.1039/C3Cc47028H |
0.561 |
|
2014 |
Ackermann L. Carboxylate-assisted ruthenium-catalyzed alkyne annulations by C-H/Het-H bond functionalizations. Accounts of Chemical Research. 47: 281-295. PMID 23379589 DOI: 10.1021/Ar3002798 |
0.46 |
|
2014 |
Ma W, Ackermann L. Silver-Mediated Alkyne Annulations by C–H/P–H Functionalizations: Step-Economical Access to Benzophospholes Synthesis. 46: 2297-2304. DOI: 10.1055/S-0033-1338630 |
0.328 |
|
2014 |
Li J, Ackermann L. Ruthenium-catalyzed oxidative alkyne annulation by C–H activation on ketimines Tetrahedron. 70: 3342-3348. DOI: 10.1016/J.Tet.2013.10.003 |
0.422 |
|
2014 |
Mondal KC, Samuel PP, Li Y, Roesky HW, Roy S, Ackermann L, Sidhu NS, Sheldrick GM, Carl E, Demeshko S, De S, Parameswaran P, Ungur L, Chibotaru LF, Andrada DM. A Catalyst with Two-Coordinate Nickel: Theoretical and Catalytic Studies European Journal of Inorganic Chemistry. 2014: 818-823. DOI: 10.1002/Ejic.201301598 |
0.436 |
|
2014 |
Gu Q, Mamari HHA, Graczyk K, Diers E, Ackermann L. Eisen‐katalysierte C(sp2)‐H‐ und C(sp3)‐H‐Arylierung mit Triazol‐Unterstützung Angewandte Chemie. 126: 3949-3952. DOI: 10.1002/Ange.201311024 |
0.467 |
|
2014 |
Sarkar SD, Liu W, Kozhushkov SI, Ackermann L. Weakly Coordinating Directing Groups for Ruthenium(II)‐ Catalyzed CH Activation Advanced Synthesis & Catalysis. 356: 1461-1479. DOI: 10.1002/Adsc.201400110 |
0.364 |
|
2014 |
Kornhaaß C, Kuper C, Ackermann L. Ferrocenylalkynes for Ruthenium-Catalyzed Isohypsic CH/NO Bond Functionalizations Advanced Synthesis & Catalysis. 356: 1619-1624. DOI: 10.1002/Adsc.201301156 |
0.311 |
|
2013 |
Musa S, Filippov OA, Belkova NV, Shubina ES, Silantyev GA, Ackermann L, Gelman D. Ligand-metal cooperating PC(sp3)P pincer complexes as catalysts in olefin hydroformylation. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 16906-9. PMID 24203915 DOI: 10.1002/Chem.201303311 |
0.321 |
|
2013 |
Ma W, Ackermann L. Ruthenium(II)-catalyzed C-H alkenylations of phenols with removable directing groups. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 13925-8. PMID 24018977 DOI: 10.1002/Chem.201301988 |
0.408 |
|
2013 |
Schinkel M, Wallbaum J, Kozhushkov SI, Marek I, Ackermann L. Carboxylate assistance for catalyzed hydroarylations of methylenecyclopropanes. Organic Letters. 15: 4482-4. PMID 23957454 DOI: 10.1021/Ol402037F |
0.495 |
|
2013 |
Punji B, Song W, Shevchenko GA, Ackermann L. Cobalt-catalyzed C-H bond functionalizations with aryl and alkyl chlorides. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 10605-10. PMID 23821432 DOI: 10.1002/Chem.201301409 |
0.776 |
|
2013 |
Liu W, Ackermann L. Ortho- and Para-Selective Ruthenium-Catalyzed C(sp2)–H Oxygenations of Phenol Derivatives Organic Letters. 15: 3484-3486. PMID 23799802 DOI: 10.1021/Ol401535K |
0.424 |
|
2013 |
Song W, Ackermann L. Nickel-catalyzed alkyne annulation by anilines: versatile indole synthesis by C–H/N–H functionalization Chemical Communications. 49: 6638-6640. PMID 23770772 DOI: 10.1039/C3Cc43915A |
0.421 |
|
2013 |
Thirunavukkarasu VS, Raghuvanshi K, Ackermann L. Expedient C-H amidations of heteroaryl arenes catalyzed by versatile ruthenium(II) catalysts. Organic Letters. 15: 3286-9. PMID 23767780 DOI: 10.1021/Ol401321Q |
0.542 |
|
2013 |
Song W, Kozhushkov SI, Ackermann L. Site‐Selective Catalytic C(sp2)H Bond Azidations Angewandte Chemie. 52: 6576-6578. PMID 23657914 DOI: 10.1002/Anie.201302015 |
0.476 |
|
2013 |
Kumar NYP, Jeyachandran R, Ackermann L. C(sp3)-H bond arylations catalyzed by well-defined [Ru(O2CMes)2(p-cymene)]. Journal of Organic Chemistry. 78: 4145-4152. PMID 23574572 DOI: 10.1021/Jo400658D |
0.467 |
|
2013 |
Hofmann N, Ackermann L. meta-Selective C–H Bond Alkylation with Secondary Alkyl Halides Journal of the American Chemical Society. 135: 5877-5884. PMID 23534668 DOI: 10.1021/Ja401466Y |
0.45 |
|
2013 |
Schinkel M, Marek I, Ackermann L. Carboxylate-assisted ruthenium(II)-catalyzed hydroarylations of unactivated alkenes through C-H cleavage. Angewandte Chemie (International Ed. in English). 52: 3977-80. PMID 23440879 DOI: 10.1002/Anie.201208446 |
0.544 |
|
2013 |
Yang F, Ackermann L. Ruthenium-catalyzed C-H oxygenation on aryl Weinreb amides. Organic Letters. 15: 718-720. PMID 23339354 DOI: 10.1021/Ol303520H |
0.472 |
|
2013 |
Wang L, Ackermann L. Versatile Pyrrole Synthesis through Ruthenium(II)-Catalyzed Alkene C–H Bond Functionalization on Enamines Organic Letters. 15: 176-179. PMID 23256885 DOI: 10.1021/Ol303224E |
0.406 |
|
2013 |
Deponti M, Kozhushkov SI, Yufit DS, Ackermann L. Ruthenium-catalyzed C–H/O–H and C–H/N–H bond functionalizations: oxidative annulations of cyclopropyl-substituted alkynes Organic and Biomolecular Chemistry. 11: 142-148. PMID 23111695 DOI: 10.1039/C2Ob26250A |
0.368 |
|
2013 |
Kozhushkov SI, Ackermann L. Ruthenium-catalyzed direct oxidative alkenylation of arenes through twofold C–H bond functionalization Chemical Science. 4: 886-896. DOI: 10.1039/C2Sc21524A |
0.404 |
|
2013 |
Kozhushkov SI, Potukuchi HK, Ackermann L. Direct C–H bond arylations and alkenylations with phenol-derived fluorine-free electrophiles Catalysis Science & Technology. 3: 562-571. DOI: 10.1039/C2Cy20505J |
0.374 |
|
2013 |
Diers E, Phani Kumar NY, Mejuch T, Marek I, Ackermann L. Carboxylate-assisted ruthenium(II)-catalyzed C-H arylations of 5-aryl tetrazoles: Step-economical access to Valsartan Tetrahedron. 69: 4445-4453. DOI: 10.1016/J.Tet.2013.01.006 |
0.537 |
|
2013 |
Song W, Kozhushkov SI, Ackermann L. Regioselektive katalytische C(sp2)‐H‐Azidierungen Angewandte Chemie. 125: 6706-6708. DOI: 10.1002/Ange.201302015 |
0.359 |
|
2012 |
Ma W, Graczyk K, Ackermann L. Ruthenium-catalyzed alkyne annulations with substituted 1H-pyrazoles by C-H/N-H bond functionalizations. Organic Letters. 14: 6318-21. PMID 23234384 DOI: 10.1021/Ol303083N |
0.526 |
|
2012 |
Thirunavukkarasu VS, Ackermann L. Ruthenium-catalyzed C-H bond oxygenations with weakly coordinating ketones. Organic Letters. 14: 6206-9. PMID 23210732 DOI: 10.1021/Ol302956S |
0.488 |
|
2012 |
Jeyachandran R, Potukuchi HK, Ackermann L. Copper-catalyzed CuAAC/intramolecular C-H arylation sequence: Synthesis of annulated 1,2,3-triazoles. Beilstein Journal of Organic Chemistry. 8: 1771-1777. PMID 23209511 DOI: 10.3762/Bjoc.8.202 |
0.458 |
|
2012 |
Li J, Kornhaaß C, Ackermann L. Ruthenium-catalyzed oxidative C–H alkenylation of aryl carbamates Chemical Communications. 48: 11343-11345. PMID 23073351 DOI: 10.1039/C2Cc36196E |
0.403 |
|
2012 |
Kornhaaß C, Li J, Ackermann L. Cationic Ruthenium Catalysts for Alkyne Annulations with Oximes by C–H/N–O Functionalizations Journal of Organic Chemistry. 77: 9190-9198. PMID 22978404 DOI: 10.1021/Jo301768B |
0.419 |
|
2012 |
Ackermann L, Kozhushkov SI, Yufit DS. Ruthenium-catalyzed hydroarylation of methylenecyclopropanes through C-H bond cleavage: scope and mechanism. Chemistry: a European Journal. 18: 12068-12077. PMID 22887713 DOI: 10.1002/Chem.201200406 |
0.467 |
|
2012 |
Thirunavukkarasu VS, Hubrich J, Ackermann L. Ruthenium-catalyzed oxidative C(sp2)-H bond hydroxylation: site-selective C-O bond formation on benzamides. Organic Letters. 14: 4210-3. PMID 22853552 DOI: 10.1021/Ol3018819 |
0.508 |
|
2012 |
Graczyk K, Ma W, Ackermann L. Oxidative alkenylation of aromatic esters by ruthenium-catalyzed twofold C-H bond cleavages. Organic Letters. 14: 4110-3. PMID 22849302 DOI: 10.1021/Ol301759V |
0.47 |
|
2012 |
Thirunavukkarasu VS, Donati M, Ackermann L. Hydroxyl-directed ruthenium-catalyzed C-H bond functionalization: versatile access to fluorescent pyrans. Organic Letters. 14: 3416-9. PMID 22691029 DOI: 10.1021/Ol301387T |
0.51 |
|
2012 |
Ackermann L, Mehta VP. Palladium-catalyzed mono-α-arylation of acetone with aryl imidazolylsulfonates. Chemistry: a European Journal. 18: 10230-10233. PMID 22615258 DOI: 10.1002/Chem.201201394 |
0.323 |
|
2012 |
Ackermann L, Pospech J, Potukuchi HK. Well-defined ruthenium(II) carboxylate as catalyst for direct C-H/C-O bond arylations with phenols in water. Organic Letters. 14: 2146-2149. PMID 22494272 DOI: 10.1021/Ol300671Y |
0.469 |
|
2012 |
Ackermann L, Kornhaass C, Zhu Y. Palladium-catalyzed direct C-H bond alkynylations of heteroarenes using gem-dichloroalkenes. Organic Letters. 14: 1824-6. PMID 22455669 DOI: 10.1021/Ol300514D |
0.496 |
|
2012 |
Ackermann L, Diers E, Manvar A. Ruthenium-catalyzed C-H bond arylations of arenes bearing removable directing groups via six-membered ruthenacycles. Organic Letters. 14: 1154-1157. PMID 22313092 DOI: 10.1021/Ol3000876 |
0.829 |
|
2012 |
Ackermann L, Pospech J, Graczyk K, Rauch K. Versatile synthesis of isocoumarins and α-pyrones by ruthenium-catalyzed oxidative C-H/O-H bond cleavages. Organic Letters. 14: 930-933. PMID 22273364 DOI: 10.1021/Ol2034614 |
0.471 |
|
2012 |
Ackermann L, Wang L, Wolfram R, Lygin AV. Ruthenium-Catalyzed Oxidative C–H Alkenylations of Anilides and Benzamides in Water Organic Letters. 14: 728-731. PMID 22264030 DOI: 10.1021/Ol203251S |
0.364 |
|
2012 |
Ackermann L, Lygin AV. Cationic ruthenium(II) catalysts for oxidative C-H/N-H bond functionalizations of anilines with removable directing group: synthesis of indoles in water. Organic Letters. 14: 764-767. PMID 22242646 DOI: 10.1021/Ol203309Y |
0.491 |
|
2012 |
Ackermann L, Wang L, Lygin AV. Ruthenium-catalyzed aerobic oxidative coupling of alkynes with 2-aryl-substituted pyrroles Chemical Science. 3: 177-180. DOI: 10.1039/C1Sc00619C |
0.377 |
|
2011 |
Ackermann L, Fenner S. Ruthenium-catalyzed C-H/N-O bond functionalization: green isoquinolone syntheses in water. Organic Letters. 13: 6548-6551. PMID 22077379 DOI: 10.1021/Ol202861K |
0.468 |
|
2011 |
Ackermann L, Pospech J. Ruthenium-Catalyzed Oxidative C–H Bond Alkenylations in Water: Expedient Synthesis of Annulated Lactones Organic Letters. 13: 4153-4155. PMID 21749083 DOI: 10.1021/Ol201563R |
0.342 |
|
2011 |
Ackermann L, Lygin AV. Ruthenium-Catalyzed Direct C–H Bond Arylations of Heteroarenes Organic Letters. 13: 3332-3335. PMID 21644545 DOI: 10.1021/Ol2010648 |
0.361 |
|
2011 |
Ackermann L, Lygin AV, Hofmann N. Ruthenium-catalyzed oxidative synthesis of 2-pyridones through C-H/N-H bond functionalizations. Organic Letters. 13: 3278-3281. PMID 21612195 DOI: 10.1021/Ol201244S |
0.498 |
|
2011 |
Ackermann L, Lygin AV, Hofmann N. Ruthenium‐Catalyzed Oxidative Annulation by Cleavage of CH/NH Bonds Angewandte Chemie. 50: 6379-6382. PMID 21612009 DOI: 10.1002/Anie.201101943 |
0.507 |
|
2011 |
Ackermann L, Barfüsser S, Kornhaass C, Kapdi AR. C–H Bond Arylations and Benzylations on Oxazol(in)es with a Palladium Catalyst of a Secondary Phosphine Oxide Organic Letters. 13: 3082-3085. PMID 21599032 DOI: 10.1021/Ol200986X |
0.435 |
|
2011 |
Ackermann L, Dell'Acqua M, Fenner S, Vicente R, Sandmann R. Metal-free direct arylations of indoles and pyrroles with diaryliodonium salts. Organic Letters. 13: 2358-60. PMID 21486075 DOI: 10.1021/Ol200601E |
0.346 |
|
2011 |
Ackermann L. Carboxylate-assisted transition-metal-catalyzed C-H bond functionalizations: mechanism and scope. Chemical Reviews. 111: 1315-1345. PMID 21391562 DOI: 10.1021/Cr100412J |
0.453 |
|
2011 |
Ackermann L, Hofmann N, Vicente R. Carboxylate-assisted ruthenium-catalyzed direct alkylations of ketimines. Organic Letters. 13: 1875-7. PMID 21388178 DOI: 10.1021/Ol200366N |
0.423 |
|
2011 |
Ackermann L, Sandmann R, Song W. Palladium- and Nickel-Catalyzed Aminations of Aryl Imidazolylsulfonates and Sulfamates Organic Letters. 13: 1784-1786. PMID 21351758 DOI: 10.1021/Ol200267B |
0.406 |
|
2011 |
Ackermann L, Kapdi AR, Fenner S, Kornhaaß C, Schulzke C. Well‐Defined Air‐Stable Palladium HASPO Complexes for Efficient Kumada–Corriu Cross‐Couplings of (Hetero)Aryl or Alkenyl Tosylates Chemistry: a European Journal. 17: 2965-2971. PMID 21294197 DOI: 10.1002/Chem.201002386 |
0.421 |
|
2011 |
Ackermann L, Fenner S. Direct arylations of electron-deficient (hetero)arenes with aryl or alkenyl tosylates and mesylates Chemical Communications. 47: 430-432. PMID 20856961 DOI: 10.1039/C0Cc02360D |
0.363 |
|
2011 |
Ackermann L, Lygin AV, Hofmann N. De Novo Ruthenium-Catalyzed Synthesis of 2-Pyridones Synfacts. 2011: 837-837. DOI: 10.1055/S-0030-1260852 |
0.365 |
|
2011 |
Ackermann L, Kozhushkov SI, Yufit DS, Marek I. Efficient Brønsted acid catalyzed hydrations and hydroaminations of (dicyclopropylmethylene)cyclopropane Synlett. 1515-1518. DOI: 10.1055/S-0030-1260769 |
0.319 |
|
2011 |
Ackermann L, Song W, Sandmann R. Nickel-catalyzed, base-mediated amination/hydroamination reaction sequence for a modular synthesis of indoles Journal of Organometallic Chemistry. 696: 195-201. DOI: 10.1016/J.Jorganchem.2010.08.047 |
0.372 |
|
2011 |
Wolpers A, Ackermann L, Vana P. H-Phosphonic Acid Derivatives as Catalysts for Reversible Chain Transfer Catalyzed Polymerization (RTCP) at Ambient and High Pressure Macromolecular Chemistry and Physics. 212: 259-265. DOI: 10.1002/Macp.201000623 |
0.368 |
|
2011 |
Ackermann L, Punji B, Song W. User‐Friendly [(Diglyme)NiBr2]‐Catalyzed Direct Alkylations of Heteroarenes with Unactivated Alkyl Halides through CH Bond Cleavages Advanced Synthesis & Catalysis. 353: 3325-3329. DOI: 10.1002/Adsc.201100487 |
0.67 |
|
2010 |
Ackermann L, Vicente R. Ruthenium-catalyzed direct arylations through C-H bond cleavages. Topics in Current Chemistry. 292: 211-29. PMID 21500408 DOI: 10.1007/128_2009_9 |
0.445 |
|
2010 |
Ackermann L, Vicente R, Potukuchi HK, Pirovano V. Mechanistic insight into direct arylations with ruthenium(II) carboxylate catalysts. Organic Letters. 12: 5032-5. PMID 20929268 DOI: 10.1021/Ol102187E |
0.433 |
|
2010 |
Ackermann L, Potukuchi HK. Regioselective syntheses of fully-substituted 1,2,3-triazoles: the CuAAC/C–H bond functionalization nexus Organic and Biomolecular Chemistry. 8: 4503-4513. PMID 20733972 DOI: 10.1039/C0Ob00212G |
0.371 |
|
2010 |
Ackermann L. Metal-catalyzed direct alkylations of (hetero)arenes via C–H bond cleavages with unactivated alkyl halides Chemical Communications. 46: 4866-4877. PMID 20532309 DOI: 10.1039/C0Cc00778A |
0.406 |
|
2010 |
Ackermann L, Kapdi AR, Schulzke C. Air-stable secondary phosphine oxide or chloride (Pre)ligands for cross-couplings of unactivated alkyl chlorides. Organic Letters. 12: 2298-2301. PMID 20405884 DOI: 10.1021/Ol100658Y |
0.351 |
|
2010 |
Ackermann L, Jeyachandran R, Potukuchi HK, Novák P, Büttner L. Palladium-catalyzed dehydrogenative direct arylations of 1,2,3-triazoles. Organic Letters. 12: 2056-2059. PMID 20356069 DOI: 10.1021/Ol1005517 |
0.389 |
|
2010 |
Ackermann L, Potukuchi HK, Althammer A, Born R, Mayer P. Tetra-ortho-Substituted Biaryls through Palladium-Catalyzed Suzuki−Miyaura Couplings with a Diaminochlorophosphine Ligand Organic Letters. 12: 1004-1007. PMID 20131821 DOI: 10.1021/Ol1000186 |
0.364 |
|
2010 |
Ackermann L, Barfüsser S, Pospech J. Palladium-catalyzed direct arylations, alkenylations, and benzylations through C-H bond cleavages with sulfamates or phosphates as electrophiles. Organic Letters. 12: 724-726. PMID 20078115 DOI: 10.1021/Ol9028034 |
0.459 |
|
2010 |
Ackermann L. Transition-metal-catalyzed direct arylations via C–H bond cleavages Pure and Applied Chemistry. 82: 1403-1413. DOI: 10.1351/Pac-Con-09-08-17 |
0.526 |
|
2010 |
Ackermann L, Novák P, Vicente R, Pirovano V, Potukuchi HK. Ruthenium-Catalyzed C-H Bond Functionalizations of 1,2,3-Triazol-4-yl-Substituted Arenes: Dehydrogenative Couplings Versus Direct Arylations Synthesis. 2010: 2245-2253. DOI: 10.1055/S-0029-1220010 |
0.51 |
|
2010 |
Ackermann L, Barfüsser S, Pospech J. Direct C-H Functionalization of Oxazoles Using Sulfamatesand Phosphates Synfacts. 2010: 694-694. DOI: 10.1055/S-0029-1219842 |
0.491 |
|
2010 |
Ackermann L, Wechsler C, Kapdi AR, Althammer A. Air-Stable DiaminophosphineSulfides as Preligands for Nickel-Catalyzed Cross-Couplings of UnactivatedFluoro(hetero)arenes Synlett. 2010: 294-298. DOI: 10.1055/S-0029-1219166 |
0.304 |
|
2010 |
Ackermann L. Air-Stable Bifunctional HASPO Preligands for Metal-Catalyzed Cross-Couplings and Direct C–H Bond Arylations Israel Journal of Chemistry. 50: 652-663. DOI: 10.1002/Ijch.201000043 |
0.355 |
|
2009 |
Ackermann L, Vicente R, Kapdi AR. Transition-metal-catalyzed direct arylation of (hetero)arenes by C-H bond cleavage. Angewandte Chemie (International Ed. in English). 48: 9792-826. PMID 19998294 DOI: 10.1002/Anie.200902996 |
0.453 |
|
2009 |
Ackermann L, Novák P. Regioselective ruthenium-catalyzed direct benzylations of arenes through C-H bond cleavages. Organic Letters. 11: 4966-4969. PMID 19810689 DOI: 10.1021/Ol902115F |
0.459 |
|
2009 |
Ackermann L, Vicente R. Catalytic direct arylations in polyethylene glycol (PEG): recyclable palladium(0) catalyst for C-H bond cleavages in the presence of air. Organic Letters. 11: 4922-5. PMID 19785433 DOI: 10.1021/Ol9020354 |
0.467 |
|
2009 |
Ackermann L, Vicente R, Hofmann N. Air-stable secondary phosphine oxide as preligand for palladium-catalyzed intramolecular alpha-arylations with chloroarenes. Organic Letters. 11: 4274-6. PMID 19775182 DOI: 10.1021/Ol901597D |
0.411 |
|
2009 |
Ackermann L, Novák P, Vicente R, Hofmann N. Ruthenium-catalyzed regioselective direct alkylation of arenes with unactivated alkyl halides through C-H bond cleavage. Angewandte Chemie (International Ed. in English). 48: 6045-8. PMID 19593835 DOI: 10.1002/Anie.200902458 |
0.529 |
|
2009 |
Ackermann L, Sandmann R, Kaspar LT. Two Titanium-Catalyzed Reaction Sequences for Syntheses of Pyrroles from (E/Z)-Chloroenynes or α-Haloalkynols Organic Letters. 11: 2031-2034. PMID 19348470 DOI: 10.1021/Ol900522G |
0.335 |
|
2009 |
Ackermann L, Born R, Vicente R. Ruthenium-catalyzed direct arylations of N-aryl 1,2,3-triazoles with aryl chlorides as electrophiles. Chemsuschem. 2: 546-9. PMID 19266510 DOI: 10.1002/Cssc.200900014 |
0.343 |
|
2009 |
Ackermann L, Althammer A, Fenner S. Palladium‐Catalyzed Direct Arylations of Heteroarenes with Tosylates and Mesylates Angewandte Chemie. 48: 201-204. PMID 19040238 DOI: 10.1002/Anie.200804517 |
0.334 |
|
2009 |
Facoetti D, Abbiati G, d’Avolio L, Ackermann L, Rossi E. TiCl4-Catalyzed Synthesis of Pyrimido[1,6-a]indol-1-ones Synfacts. 2009: 1196-1196. DOI: 10.1055/S-0029-1218137 |
0.362 |
|
2009 |
Ackermann L, Potukuchi HK. Palladium-Catalyzed Cross-CouplingReactions of 2-Pyridylborates with Air-Stable HASPO Preligands Synlett. 2009: 2852-2856. DOI: 10.1055/S-0029-1218020 |
0.342 |
|
2009 |
Facoetti D, Abbiati G, d’Avolio L, Ackermann L, Rossi E. Novel Domino Approach to FluorescentPyrimido[1,6-a]indolones Synlett. 2009: 2273-2276. DOI: 10.1055/S-0029-1217807 |
0.335 |
|
2009 |
Ackermann L, Sandmann R, Kaspar LT. Titanium-Catalyzed Intermolecular Hydroamination Route toPyrroles Synfacts. 2009: 718-718. DOI: 10.1055/S-0029-1217384 |
0.342 |
|
2009 |
Ackermann L, Althammer A, Mayer P. Palladium-Catalyzed DirectArylation-Based Domino Synthesis of Annulated N-HeterocyclesUsing Alkenyl or (Hetero)Aryl 1,2-Dihalides Synthesis. 2009: 3493-3503. DOI: 10.1055/S-0029-1216977 |
0.401 |
|
2009 |
Ackermann L, Sandmann R, Kondrashov MV. Thieme Chemistry Journal Awardees - WhereAre They Now? Palladium-Catalyzed N-Arylation-HydroaminationSequence for the Synthesis of Indoles with StericallyDemanding N-Substituents Synlett. 2009: 1219-1222. DOI: 10.1055/S-0029-1216727 |
0.326 |
|
2009 |
Ackermann L, Barfüßer S. Palladium-Catalyzed DirectC-3 Arylations of Indoles with an Air-Stable HASPO Synlett. 2009: 808-812. DOI: 10.1055/S-0028-1087951 |
0.437 |
|
2009 |
Ackermann L, Sandmann R, Schinkel M, Kondrashov MV. Palladium-catalyzed sequential indole synthesis using sterically hindered amines Tetrahedron. 65: 8930-8939. DOI: 10.1016/J.Tet.2009.07.073 |
0.368 |
|
2009 |
Ackermann L, Althammer A. Moderne Magnesiumorganische Chemie. Neues von der Grignard‐Reaktion Chemie in Unserer Zeit. 43: 74-83. DOI: 10.1002/Ciuz.200900476 |
0.404 |
|
2009 |
Ackermann L, Vicente R, Kapdi AR. Übergangsmetallkatalysierte direkte Arylierungen von (Hetero)Arenen durch C‐H‐Bindungsbruch Angewandte Chemie. 121: 9976-10011. DOI: 10.1002/Ange.200902996 |
0.415 |
|
2009 |
Ackermann L, Barfüßer S, Potukuchi HK. Copper‐Catalyzed N‐Arylation/Hydroamin(d)ation Domino Synthesis of Indoles and its Application to the Preparation of a Chek1/KDR Kinase Inhibitor Pharmacophore Advanced Synthesis & Catalysis. 351: 1064-1072. DOI: 10.1002/Adsc.200900004 |
0.357 |
|
2008 |
Ackermann L, Mulzer M. Dehydrative direct arylations of arenes with phenols via ruthenium-catalyzed C-H and C-OH bond functionalizations. Organic Letters. 10: 5043-5045. PMID 18855399 DOI: 10.1021/Ol802252M |
0.504 |
|
2008 |
Kozhushkov SI, Yufit DS, Ackermann L. Ruthenium-Catalyzed Hydroarylations of Methylenecyclopropanes: Mild C−H Bond Functionalizations with Conservation of Cyclopropane Rings Organic Letters. 10: 3409-3412. PMID 18630917 DOI: 10.1021/Ol8011875 |
0.33 |
|
2008 |
Ackermann L, Potukuchi HK, Landsberg D, Vicente R. Copper-catalyzed "click" reaction/direct arylation sequence: modular syntheses of 1,2,3-triazoles. Organic Letters. 10: 3081-4. PMID 18549230 DOI: 10.1021/Ol801078R |
0.366 |
|
2008 |
Ackermann L, Vicente R, Althammer A. Assisted ruthenium-catalyzed C-H bond activation: carboxylic acids as cocatalysts for generally applicable direct arylations in apolar solvents. Organic Letters. 10: 2299-302. PMID 18439021 DOI: 10.1021/Ol800773X |
0.482 |
|
2008 |
Ackermann L, Althammer A. Phosphoric Acid Diesters as Efficient Catalysts for Hydroaminations of Nonactivated Alkenes and an Application to Asymmetric Hydroaminations Synlett. 2008: 995-998. DOI: 10.1055/S-2008-1072505 |
0.341 |
|
2008 |
Ackermann L, Sandmann R, Villar A, Kaspar LT. Hydroamination-Heck Annulation Route to 3-Substituted Indoles Synfacts. 2008: 355-355. DOI: 10.1055/S-2008-1042857 |
0.312 |
|
2008 |
Ackermann L, Althammer A, Born R. [RuCl3(H2O)n] -catalyzed direct arylations Tetrahedron. 64: 6115-6124. DOI: 10.1016/J.Tet.2008.01.050 |
0.382 |
|
2008 |
Ackermann L, Sandmann R, Villar A, Kaspar LT. Annulation of internal alkynes through a hydroamination/aza-Heck reaction sequence for the regioselective synthesis of indoles Tetrahedron. 64: 769-777. DOI: 10.1016/J.Tet.2007.10.117 |
0.375 |
|
2008 |
Ackermann L, Vicente R, Born R. Palladium‐Catalyzed Direct Arylations of 1,2,3‐Triazoles with Aryl Chlorides using Conventional Heating Advanced Synthesis & Catalysis. 350: 741-748. DOI: 10.1002/Adsc.200800016 |
0.431 |
|
2007 |
Ackermann L, Born R, Álvarez‐Bercedo P. Ruthenium(IV) alkylidenes as precatalysts for direct arylations of alkenes with aryl chlorides and an application to sequential catalysis. Angewandte Chemie. 46: 6364-6367. PMID 17640018 DOI: 10.1002/Anie.200701727 |
0.397 |
|
2007 |
Ackermann L, Kaspar LT. TiCl4-catalyzed indirect anti-Markovnikov hydration of alkynes: application to the synthesis of benzo[b]furans. Journal of Organic Chemistry. 72: 6149-6153. PMID 17629343 DOI: 10.1021/Jo070887I |
0.355 |
|
2007 |
Ackermann L, Kaspar LT, Althammer A. Hydroaminations of unactivated alkenes with basic alkylamines: group 4 metal halide catalysts and Brønsted-acid organocatalysts Organic and Biomolecular Chemistry. 5: 1975-1978. PMID 17551648 DOI: 10.1039/B706301F |
0.349 |
|
2007 |
Ackermann L, Althammer A. Domino N-H/C-H bond activation: palladium-catalyzed synthesis of annulated heterocycles using dichloro(hetero)arenes. Angewandte Chemie. 46: 1627-1629. PMID 17397073 DOI: 10.1002/Anie.200603833 |
0.528 |
|
2007 |
Ackermann L, Althammer A, Born R. [RuCl3(H2O)n]-Catalyzed Direct Arylations with Bromides as Electrophiles Synlett. 2007: 2833-2836. DOI: 10.1055/S-2007-990838 |
0.487 |
|
2007 |
Ackermann L. Catalytic Arylations with Challenging Substrates: From Air-Stable HASPO Preligands to Indole Syntheses and C-H-Bond Functionalizations Synlett. 2007: 507-526. DOI: 10.1055/S-2007-970744 |
0.478 |
|
2006 |
Ackermann L, Spatz JH, Gschrei CJ, Born R, Althammer A. A Diaminochlorophosphine for Palladium‐Catalyzed Arylations of Amines and Ketones Angewandte Chemie. 45: 7627-7630. PMID 17044111 DOI: 10.1002/Anie.200602222 |
0.385 |
|
2006 |
Ackermann L, Gschrei CJ, Althammer A, Riederer M. Cross-coupling reactions of aryl and vinyl chlorides catalyzed by a palladium complex derived from an air-stable H-phosphonate. Chemical Communications. 1419-21. PMID 16550286 DOI: 10.1039/B518283B |
0.427 |
|
2006 |
Ackermann L, Althammer A, Born R. Catalytic arylation reactions by C-H bond activation with aryl tosylates. Angewandte Chemie. 45: 2619-2622. PMID 16544353 DOI: 10.1002/Anie.200504450 |
0.53 |
|
2006 |
Ackermann L, Born R, Spatz JH, Althammer A, Gschrei CJ. Air-stable phosphine oxides as preligands for catalytic activation reactions of C-Cl, C-F, and C-H bonds Pure and Applied Chemistry. 78: 209-214. DOI: 10.1351/Pac200678020209 |
0.504 |
|
2006 |
Ackermann L, Althammer A. One-Pot 2-Aryl/Vinylindole Synthesis Consisting of a Ruthenium-Catalyzed Hydroamination and a Palladium-Catalyzed Heck Reaction Using 2-Chloroaniline Synlett. 2006: 3125-3129. DOI: 10.1055/S-2006-950440 |
0.392 |
|
2006 |
Ackermann L. Air- and moisture-stable secondary phosphine oxides as preligands in catalysis Synthesis. 2006: 1557-1571. DOI: 10.1055/S-2006-926427 |
0.308 |
|
2005 |
Ackermann L, Born R, Spatz JH, Meyer D. Efficient aryl-(hetero)aryl coupling by activation of C-Cl and C-F bonds using nickel complexes of air-stable phosphine oxides. Angewandte Chemie (International Ed. in English). 44: 7216-9. PMID 16229046 DOI: 10.1002/Anie.200501860 |
0.443 |
|
2005 |
Kaspar LT, Fingerhut B, Ackermann L. Titanium-catalyzed intermolecular hydroamination of vinylarenes. Angewandte Chemie. 44: 5972-5974. PMID 16097016 DOI: 10.1002/Anie.200501423 |
0.392 |
|
2005 |
Ackermann L. Phosphine Oxides as Preligands in Ruthenium-Catalyzed Arylations via C−H Bond Functionalization Using Aryl Chlorides Organic Letters. 7: 3123-3125. PMID 15987221 DOI: 10.1021/Ol051216E |
0.407 |
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2005 |
Ackermann L, Born R. Modular diamino- and dioxophosphine oxides and chlorides as ligands for transition-metal-catalyzed C--C and C--N couplings with aryl chlorides. Angewandte Chemie. 44: 2444-2447. PMID 15770635 DOI: 10.1002/Anie.200462371 |
0.439 |
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2005 |
Ackermann L. General and efficient indole syntheses based on catalytic amination reactions. Organic Letters. 7: 439-442. PMID 15673259 DOI: 10.1021/Ol047649J |
0.401 |
|
2005 |
Kaspar LT, Ackermann L. Three-component indole synthesis using ortho-dihaloarenes Tetrahedron. 61: 11311-11316. DOI: 10.1016/J.Tet.2005.09.095 |
0.338 |
|
2004 |
Ackermann L, Kaspar LT, Gschrei CJ. Hydroamination/Heck reaction sequence for a highly regioselective one-pot synthesis of indoles using 2-chloroaniline Chemical Communications. 2824-5. PMID 15599425 DOI: 10.1039/B411571F |
0.383 |
|
2004 |
Ackermann L, Kaspar LT, Gschrei CJ. TiCl4-catalyzed intermolecular hydroamination reactions of norbornene. Organic Letters. 6: 2515-2518. PMID 15255679 DOI: 10.1021/Ol049282O |
0.353 |
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2004 |
Ackermann L, Born R. TiCl4/t-BuNH2 as the sole catalyst for a hydroamination-based Fischer indole synthesis Tetrahedron Letters. 45: 9541-9544. DOI: 10.1016/J.Tetlet.2004.10.160 |
0.348 |
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2003 |
Ackermann L, Bergman RG, Loy RN. Use of group 4 bis(sulfonamido) complexes in the intramolecular hydroamination of alkynes and allenes. Journal of the American Chemical Society. 125: 11956-63. PMID 14505417 DOI: 10.1021/Ja0361547 |
0.525 |
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2003 |
Ackermann L. TiCl4-Catalyzed Intermolecular Hydroamination Reactions Organometallics. 22: 4367-4368. DOI: 10.1021/Om034143G |
0.361 |
|
2002 |
Fürstner A, Krause H, Ackermann L, Lehmann CW. N-Heterocyclic carbenes can coexist with alkenes and C-H acidic sites. Chemical Communications (Cambridge, England). 2240-1. PMID 12240130 DOI: 10.1039/B107238B |
0.58 |
|
2002 |
Ackermann L, Bergman RG. A highly reactive titanium precatalyst for intramolecular hydroamination reactions. Organic Letters. 4: 1475-8. PMID 11975607 DOI: 10.1021/Ol0256724 |
0.503 |
|
2001 |
Fürstner A, Ackermann L, Beck K, Hori H, Koch D, Langemann K, Liebl M, Six C, Leitner W. Olefin metathesis in supercritical carbon dioxide. Journal of the American Chemical Society. 123: 9000-6. PMID 11552807 DOI: 10.1021/Ja010952K |
0.565 |
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2001 |
Fürstner A, Ackermann L, Gabor B, Goddard R, Lehmann CW, Mynott R, Stelzer F, Thiel OR. Comparative investigation of ruthenium-based metathesis catalysts bearing N-heterocyclic carbene (NHC) ligands. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 3236-53. PMID 11531110 DOI: 10.1002/1521-3765(20010803)7:15<3236::Aid-Chem3236>3.0.Co;2-S |
0.541 |
|
2001 |
Fürstner A, Thiel OR, Ackermann L. Exploiting the reversibility of olefin metathesis. Syntheses of macrocyclic trisubstituted alkenes and (R,R)-(-)-pyrenophorin. Organic Letters. 3: 449-51. PMID 11428036 DOI: 10.1021/Ol0069554 |
0.518 |
|
2000 |
Furstner A, Thiel OR, Ackermann L, Schanz HJ, Nolan SP. Ruthenium carbene complexes with N,N'-bis(mesityl)imidazol-2-ylidene ligands: RCM catalysts of extended scope The Journal of Organic Chemistry. 65: 2204-7. PMID 10774047 DOI: 10.1021/Jo9918504 |
0.546 |
|
2000 |
Ackermann L, El Tom D, Fürstner A. Ruthenium Carbene Complexes with Imidazol-2-ylidene Ligands: Syntheses of Conduritol Derivatives Reveals Superior RCM Activity Tetrahedron. 56: 2195-2202. DOI: 10.1016/S0040-4020(99)01102-3 |
0.555 |
|
1999 |
Fürstner A, Ackermann L. A most user-friendly protocol for ring closing metathesis reactions Chemical Communications. 95-96. DOI: 10.1039/A808810A |
0.497 |
|
1999 |
Ackermann L, Heidbreder A, Wurche F, Klärner F, Mattay J. Mechanistic studies on PET-oxidative cyclization of unsaturated silyl enol ethers: dependence of the regioselectivity on alcohol addition and pressure effects Journal of the Chemical Society-Perkin Transactions 1. 863-870. DOI: 10.1039/A807683I |
0.301 |
|
1999 |
Ackermann L, Fürstner A, Weskamp T, Kohl FJ, Herrmann WA. Ruthenium carbene complexes with imidazolin-2-ylidene ligands allow the formation of tetrasubstituted cycloalkenes by RCM Tetrahedron Letters. 40: 4787-4790. DOI: 10.1016/S0040-4039(99)00919-3 |
0.552 |
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