| Year |
Citation |
Score |
| 2023 |
Rogova T, Ahrweiler E, Schoetz MD, Schoenebeck F. Recent Developments with Organogermanes: their Preparation and Application in Synthesis and Catalysis. Angewandte Chemie (International Ed. in English). e202314709. PMID 37899306 DOI: 10.1002/anie.202314709 |
0.32 |
|
| 2022 |
Mendel M, Gnägi L, Dabranskaya U, Schoenebeck F. Rapid and Modular Access to Vinyl Cyclopropanes Enabled by Air-stable Palladium(I) Dimer Catalysis. Angewandte Chemie (International Ed. in English). PMID 36226918 DOI: 10.1002/anie.202211167 |
0.44 |
|
| 2021 |
Kundu G, Opincal F, Sperger T, Schoenebeck F. Air-Stable Pd Dimer Enabled Remote Functionalization: Access to Fluorinated 1,1-Diaryl Alkanes with Unprecedented Speed. Angewandte Chemie (International Ed. in English). PMID 34735037 DOI: 10.1002/anie.202113667 |
0.456 |
|
| 2021 |
Dahiya A, Schoenebeck F. Base-Mediated Direct C-H Germylation of Heteroarenes and Arenes. Organic Letters. 23: 6010-6013. PMID 34255534 DOI: 10.1021/acs.orglett.1c02079 |
0.303 |
|
| 2021 |
Schoenebeck F. Base-Free Cross-Couplings of Aryl Diazonium Salts in Methanol: Pd(II)-Alkoxy as Reactivity-Controlling Intermediate. Angewandte Chemie (International Ed. in English). PMID 33543508 DOI: 10.1002/anie.202014842 |
0.439 |
|
| 2020 |
Fricke C, Schoenebeck F. Organogermanes as Orthogonal Coupling Partners in Synthesis and Catalysis. Accounts of Chemical Research. PMID 33118804 DOI: 10.1021/acs.accounts.0c00527 |
0.465 |
|
| 2020 |
Fricke C, Sperger T, Mendel M, Schoenebeck F. Catalysis with Palladium(I) Dimers. Angewandte Chemie (International Ed. in English). PMID 33058375 DOI: 10.1002/anie.202011825 |
0.53 |
|
| 2020 |
Kundu G, Sperger T, Rissanen K, Schoenebeck F. Next Generation Air-Stable Pd(I) Dimer Enables Olefin Migrations & Selective C-C Couplings in Air. Angewandte Chemie (International Ed. in English). PMID 32810335 DOI: 10.1002/Anie.202009115 |
0.513 |
|
| 2020 |
Fricke C, Deckers K, Schoenebeck F. Orthogonal Stability & Reactivity of Aryl Germanes Enables Rapid and Selective (Multi)Halogenations. Angewandte Chemie (International Ed. in English). PMID 32656881 DOI: 10.1002/Anie.202008372 |
0.357 |
|
| 2020 |
Selmani A, Gevondian AG, Schoenebeck F. Germylation of Arenes via Pd(I) Dimer Enabled Sulfonium Salt Functionalization. Organic Letters. 22: 4802-4805. PMID 32491868 DOI: 10.1021/Acs.Orglett.0C01609 |
0.517 |
|
| 2020 |
Sherborne GJ, Gevondian AG, Funes-Ardoiz I, Dahiya A, Fricke C, Schoenebeck F. Modular & Selective Arylation of Aryl Germanes (C-GeEt3) over C-Bpin, C-SiR3 and Halogens enabled by Light-Activated Gold-Catalysis. Angewandte Chemie (International Ed. in English). PMID 32392397 DOI: 10.1002/Anie.202005066 |
0.44 |
|
| 2020 |
Dahiya A, Fricke C, Schoenebeck F. Gold-catalyzed Chemoselective Couplings of Polyfluoroarenes with Aryl Germanes and Downstream Diversification. Journal of the American Chemical Society. PMID 32249568 DOI: 10.1021/Jacs.0C02860 |
0.332 |
|
| 2020 |
Kalvet I, Deckers K, Funes-Ardoiz I, Magnin G, Sperger T, Kremer M, Schoenebeck F. Selective Ortho Functionalization of Adamantylarenes enabled by Dispersion and an Air-Stable Pd(I) Dimer. Angewandte Chemie (International Ed. in English). PMID 32065717 DOI: 10.1002/Anie.202001326 |
0.547 |
|
| 2019 |
Mendel M, Kalvet I, Hupperich D, Magnin G, Schoenebeck F. Site-Selective, Modular Diversification of Polyhalogenated Aryl Fluorosulfates (ArOSO2F) enabled by an Air-Stable Pd(I) Dimer. Angewandte Chemie (International Ed. in English). PMID 31733009 DOI: 10.1002/Anie.201911465 |
0.508 |
|
| 2019 |
Fricke C, Dahiya A, Reid WB, Schoenebeck F. Gold-Catalyzed C-H Functionalization with Aryl Germanes. Acs Catalysis. 9: 9231-9236. PMID 31608162 DOI: 10.1021/Acscatal.9B02841 |
0.454 |
|
| 2019 |
Fricke C, Sherborne G, Funes-Ardoiz I, Senol E, Guven S, Schoenebeck F. Orthogonal Nanoparticle Catalysis with Organogermaniums. Angewandte Chemie (International Ed. in English). PMID 31562670 DOI: 10.1002/Anie.201910060 |
0.365 |
|
| 2019 |
Chen XY, Pu M, Cheng HG, Sperger T, Schoenebeck F. Arylation of Axially Chiral Phosphorothioate Salts via Dinuclear Pd(I) Catalysis. Angewandte Chemie (International Ed. in English). PMID 31190467 DOI: 10.1002/Anie.201906063 |
0.573 |
|
| 2019 |
Magnin G, Clifton J, Schoenebeck F. A General and Air-tolerant Strategy to Conjugated Polymers within Seconds under Pd(I) Dimer Catalysis. Angewandte Chemie (International Ed. in English). PMID 31112626 DOI: 10.1002/Anie.201903765 |
0.454 |
|
| 2019 |
Senol E, Scattolin T, Schoenebeck F. Selenolation of Aryl Iodides and Bromides Enabled by a Bench-Stable Pd(I) Dimer. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30913326 DOI: 10.1002/Chem.201900951 |
0.608 |
|
| 2019 |
Kapat A, Sperger T, Guven S, Schoenebeck F. -Olefins through intramolecular radical relocation. Science (New York, N.Y.). 363: 391-396. PMID 30679370 DOI: 10.1126/Science.Aav1610 |
0.764 |
|
| 2019 |
Fricke C, Dahiya A, Reid WB, Schoenebeck F. Correction to “Gold-Catalyzed C–H Functionalization with Aryl Germanes” Acs Catalysis. 9: 10232-10232. DOI: 10.1021/Acscatal.9B04259 |
0.316 |
|
| 2019 |
Agasti S, Mondal B, Achar TK, Sinha SK, Sarala Suseelan A, Szabo KJ, Schoenebeck F, Maiti D. Orthogonal Selectivity in C–H Olefination: Synthesis of Branched Vinylarene with Unactivated Aliphatic Substitution Acs Catalysis. 9: 9606-9613. DOI: 10.1021/Acscatal.9B03019 |
0.365 |
|
| 2019 |
Mendel M, Kalvet I, Hupperich D, Magnin G, Schoenebeck F. Chemoselektive, modulare Diversifikation polyhalogenierter Arylfluorosulfate (ArOSO
2
F), ermöglicht durch ein luftstabiles Pd
I
‐Dimer Angewandte Chemie. 132: 2132-2136. DOI: 10.1002/Ange.201911465 |
0.479 |
|
| 2018 |
Diehl CJ, Scattolin T, Englert U, Schoenebeck F. C-I Selective Cross-Coupling Enabled by a Cationic Pd Trimer. Angewandte Chemie (International Ed. in English). PMID 30381881 DOI: 10.1002/Anie.201811380 |
0.579 |
|
| 2018 |
Sperger T, Guven S, Schoenebeck F. Chemoselective Pd-Catalyzed C-TeCF3 Coupling of Aryl Iodides. Angewandte Chemie (International Ed. in English). PMID 30346648 DOI: 10.1002/Anie.201810950 |
0.548 |
|
| 2018 |
Pu M, Sanhueza I, Senol E, Schoenebeck F. Divergent Reactivity of Stannane and Silane in the Trifluoromethylation of Pd(II): Cyclic Transition State versus Difluorocarbene Release. Angewandte Chemie (International Ed. in English). PMID 30207033 DOI: 10.1002/Anie.201808229 |
0.809 |
|
| 2018 |
Keaveney ST, Kundu G, Schoenebeck F. Modular Functionalization of Arenes in a Triply Selective Sequence: Rapid Csp2 and Csp3 Coupling of C-Br, C-OTf & C-Cl enabled by a Single Pd(I) dimer. Angewandte Chemie (International Ed. in English). PMID 30091504 DOI: 10.1002/Anie.201808386 |
0.43 |
|
| 2018 |
Ye J, Kalvet I, Schoenebeck F, Rovis T. Direct α-alkylation of primary aliphatic amines enabled by CO and electrostatics. Nature Chemistry. PMID 30061617 DOI: 10.1038/S41557-018-0085-9 |
0.337 |
|
| 2018 |
Scattolin T, Senol E, Yin G, Guo Q, Schoenebeck F. Site-Selective C-S Bond Formation at C-Br over C-OTf and C-Cl Enabled by an Air-Stable, Easy-to-Recover & Recyclable Pd(I) Catalyst. Angewandte Chemie (International Ed. in English). PMID 30014554 DOI: 10.1002/Anie.201806036 |
0.56 |
|
| 2018 |
Keaveney S, Schoenebeck F. Palladium-Catalyzed Decarbonylative Trifluoromethylation of Acid Fluorides. Angewandte Chemie (International Ed. in English). PMID 29479784 DOI: 10.1002/Anie.201800644 |
0.561 |
|
| 2018 |
Schoenebeck F, Sperger T. α-Arylation of Esters and Ketones Enabled by a Bench-Stable Pd(I) Dimer Catalyst Synthesis. 50: 4471-4475. DOI: 10.1055/S-0037-1610087 |
0.518 |
|
| 2018 |
Boshkow J, Scattolin T, Schoenebeck F, Carreira EM. [1,3]-Sigmatropic Shift of an Allylic Chloride Helvetica Chimica Acta. 101: e1800148. DOI: 10.1002/Hlca.201800148 |
0.328 |
|
| 2017 |
Scattolin T, Deckers K, Schoenebeck F. Direct Synthesis of Acyl Fluorides from Carboxylic Acids with the Bench-Stable Solid Reagent (Me4N)SCF3. Organic Letters. 19: 5740-5743. PMID 29023131 DOI: 10.1021/Acs.Orglett.7B02516 |
0.329 |
|
| 2017 |
Dürr AB, Fisher HC, Kalvet I, Truong KN, Schoenebeck F. Striking Divergence in Reactivity of a Dinuclear (NHC)Ni(I) Catalyst vs Ni(0) enables Chemoselective Trifluoromethylselenolation. Angewandte Chemie (International Ed. in English). PMID 28795520 DOI: 10.1002/Ange.201706423 |
0.322 |
|
| 2017 |
Kalvet I, Sperger T, Scattolin T, Magnin G, Schoenebeck F. Palladium(I) Dimer Enabled Extremely Rapid and Chemoselective Alkylation of Aryl Bromides over Triflates and Chlorides in Air. Angewandte Chemie (International Ed. in English). 56: 7078-7082. PMID 28508520 DOI: 10.1002/Anie.201701691 |
0.533 |
|
| 2017 |
Sperger T, Le CM, Lautens M, Schoenebeck F. Mechanistic insights on the Pd-catalyzed addition of C-X bonds across alkynes - a combined experimental and computational study. Chemical Science. 8: 2914-2922. PMID 28451357 DOI: 10.1039/C6Sc05001H |
0.587 |
|
| 2017 |
Gemoets HPL, Kalvet I, Nyuchev AV, Erdmann N, Hessel V, Schoenebeck F, Noël T. Mild and selective base-free C-H arylation of heteroarenes: experiment and computation. Chemical Science. 8: 1046-1055. PMID 28451243 DOI: 10.1039/C6Sc02595A |
0.466 |
|
| 2017 |
Ye J, Shi Z, Sperger T, Yasukawa Y, Kingston C, Schoenebeck F, Lautens M. Remote C-H alkylation and C-C bond cleavage enabled by an in situ generated palladacycle. Nature Chemistry. 9: 361-368. PMID 28338687 DOI: 10.1038/Nchem.2631 |
0.33 |
|
| 2017 |
Johansson Seechurn CC, Sperger T, Scrase TG, Schoenebeck F, Colacot TJ. Understanding the Unusual Reduction Mechanism of Pd(II) to Pd(I): Uncovering Hidden Species and Implications in Catalytic Cross-Coupling Reactions. Journal of the American Chemical Society. PMID 28300400 DOI: 10.1021/Jacs.7B01110 |
0.604 |
|
| 2017 |
Kalvet I, Guo Q, Tizzard GJ, Schoenebeck F. When Weaker Can Be Tougher: The Role of Oxidation State (I) in P- vs N-Ligand-Derived Ni-Catalyzed Trifluoromethylthiolation of Aryl Halides. Acs Catalysis. 7: 2126-2132. PMID 28286695 DOI: 10.1021/Acscatal.6B03344 |
0.361 |
|
| 2017 |
Kalvet I, Magnin G, Schoenebeck F. Rapid Room-Temperature, Chemoselective Csp2 -Csp2 Coupling of Poly(pseudo)halogenated Arenes Enabled by Palladium(I) Catalysis in Air. Angewandte Chemie (International Ed. in English). 56: 1581-1585. PMID 28032945 DOI: 10.1002/Anie.201609635 |
0.551 |
|
| 2017 |
Scattolin T, Deckers K, Schoenebeck F. Efficient Synthesis of Trifluoromethyl Amines through a Formal Umpolung Strategy from the Bench-Stable Precursor (Me4 N)SCF3. Angewandte Chemie (International Ed. in English). 56: 221-224. PMID 27936300 DOI: 10.1002/Anie.201609480 |
0.313 |
|
| 2016 |
Dürr AB, Yin G, Kalvet I, Napoly F, Schoenebeck F. Nickel-catalyzed trifluoromethylthiolation of Csp(2)-O bonds. Chemical Science. 7: 1076-1081. PMID 29081943 DOI: 10.1039/C5Sc03359D |
0.335 |
|
| 2016 |
Le CM, Sperger T, Fu R, Hou X, Lim YH, Schoenebeck F, Lautens M. Stereoselective Synthesis of Methylene Oxindoles via Palladium(II)-Catalyzed Intramolecular Cross-Coupling of Carbamoyl Chlorides. Journal of the American Chemical Society. PMID 27700076 DOI: 10.1021/Jacs.6B08925 |
0.566 |
|
| 2016 |
Sperger T, Sanhueza IA, Schoenebeck F. Computation and Experiment: A Powerful Combination to Understand and Predict Reactivities. Accounts of Chemical Research. 49: 1311-9. PMID 27171796 DOI: 10.1021/Acs.Accounts.6B00068 |
0.84 |
|
| 2016 |
Liu X, Hsiao CC, Kalvet I, Leiendecker M, Guo L, Schoenebeck F, Rueping M. Lewis Acid Assisted Nickel-Catalyzed Cross-Coupling of Aryl Methyl Ethers by C-O Bond-Cleaving Alkylation: Prevention of Undesired β-Hydride Elimination. Angewandte Chemie (International Ed. in English). PMID 27062726 DOI: 10.1002/Anie.201510497 |
0.35 |
|
| 2016 |
Schoenebeck F, Sperger T, Stirner C. Bench-Stable and Recoverable Palladium(I) Dimer as an Efficient Catalyst for Heck Cross-Coupling Synthesis. 49: 115-120. DOI: 10.1055/S-0036-1588318 |
0.45 |
|
| 2016 |
Sperger T, Fisher HC, Schoenebeck F. Computationally deciphering palladium-catalyzed reaction mechanisms Wiley Interdisciplinary Reviews: Computational Molecular Science. 6: 226-242. DOI: 10.1002/Wcms.1244 |
0.582 |
|
| 2015 |
Hack D, Dürr AB, Deckers K, Chauhan P, Seling N, Rübenach L, Mertens L, Raabe G, Schoenebeck F, Enders D. Asymmetric Synthesis of Spiropyrazolones by Sequential Organo- and Silver Catalysis. Angewandte Chemie (International Ed. in English). PMID 26676875 DOI: 10.1002/Anie.201510602 |
0.378 |
|
| 2015 |
Tsang AS, Kapat A, Schoenebeck F. Factors that Control C-C Cleavage versus C-H Bond Hydroxlyation in Copper-Catalyzed Oxidations of Ketones with O2. Journal of the American Chemical Society. PMID 26675262 DOI: 10.1021/Jacs.5B08347 |
0.776 |
|
| 2015 |
Le CM, Hou X, Sperger T, Schoenebeck F, Lautens M. An Exclusively trans-Selective Chlorocarbamoylation of Alkynes Enabled by a Palladium/Phosphaadamantane Catalyst. Angewandte Chemie (International Ed. in English). PMID 26585593 DOI: 10.1002/Anie.201507883 |
0.396 |
|
| 2015 |
Hendriks CM, Penning TM, Zang T, Wiemuth D, Gründer S, Sanhueza IA, Schoenebeck F, Bolm C. Pentafluorosulfanyl-containing flufenamic acid analogs: Syntheses, properties and biological activities. Bioorganic & Medicinal Chemistry Letters. PMID 26372652 DOI: 10.1016/J.Bmcl.2015.09.012 |
0.711 |
|
| 2015 |
Sperger T, Sanhueza IA, Kalvet I, Schoenebeck F. Computational Studies of Synthetically Relevant Homogeneous Organometallic Catalysis Involving Ni, Pd, Ir, and Rh: An Overview of Commonly Employed DFT Methods and Mechanistic Insights. Chemical Reviews. 115: 9532-86. PMID 26207572 DOI: 10.1021/Acs.Chemrev.5B00163 |
0.817 |
|
| 2015 |
Aufiero M, Sperger T, Tsang AS, Schoenebeck F. Highly Efficient CSeCF3 Coupling of Aryl Iodides Enabled by an Air-Stable Dinuclear Pd(I) Catalyst. Angewandte Chemie (International Ed. in English). PMID 26118426 DOI: 10.1002/Anie.201503388 |
0.857 |
|
| 2015 |
Yin G, Kalvet I, Schoenebeck F. Trifluoromethylthiolation of aryl iodides and bromides enabled by a bench-stable and easy-to-recover dinuclear palladium(I) catalyst. Angewandte Chemie (International Ed. in English). 54: 6809-13. PMID 25913653 DOI: 10.1002/Anie.201501617 |
0.603 |
|
| 2015 |
Yin G, Kalvet I, Englert U, Schoenebeck F. Fundamental studies and development of nickel-catalyzed trifluoromethylthiolation of aryl chlorides: active catalytic species and key roles of ligand and traceless MeCN additive revealed. Journal of the American Chemical Society. 137: 4164-72. PMID 25790253 DOI: 10.1021/Jacs.5B00538 |
0.371 |
|
| 2015 |
Chiu M, Tchitchanov BH, Zimmerli D, Sanhueza IA, Schoenebeck F, Trapp N, Schweizer WB, Diederich F. Strain-accelerated formation of chiral, optically active buta-1,3-dienes. Angewandte Chemie (International Ed. in English). 54: 349-54. PMID 25425560 DOI: 10.1002/Anie.201409289 |
0.731 |
|
| 2015 |
Aufiero M, Scattolin T, Proutière F, Schoenebeck F. Air-Stable Dinuclear Iodine-Bridged Pd(I) Complex - Catalyst, Precursor, or Parasite? The Additive Decides. Systematic Nucleophile-Activity Study and Application as Precatalyst in Cross-Coupling Organometallics. 34: 5191-5195. DOI: 10.1021/Acs.Organomet.5B00766 |
0.834 |
|
| 2015 |
Chiu M, Tchitchanov BH, Zimmerli D, Sanhueza IA, Schoenebeck F, Trapp N, Schweizer WB, Diederich F. Strain-accelerated formation of chiral, optically active buta-1,3-dienes Angewandte Chemie - International Edition. 54: 349-354. DOI: 10.1002/anie.201409289 |
0.675 |
|
| 2015 |
Aufiero M, Sperger T, Tsang AS, Schoenebeck F. Hoch effiziente C-SeCF3-Kupplung von Aryliodiden durch einen luftbeständigen zweikernigen PdI-Katalysator Angewandte Chemie. 127: 10462-10466. DOI: 10.1002/Ange.201503388 |
0.747 |
|
| 2014 |
Tsang AS, Sanhueza IA, Schoenebeck F. Combining experimental and computational studies to understand and predict reactivities of relevance to homogeneous catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 16432-41. PMID 25345971 DOI: 10.1002/Chem.201404725 |
0.724 |
|
| 2014 |
Kalvet I, Bonney KJ, Schoenebeck F. Kinetic and computational studies on Pd(I) dimer-mediated halogen exchange of aryl iodides. The Journal of Organic Chemistry. 79: 12041-6. PMID 25247472 DOI: 10.1021/Jo501889J |
0.853 |
|
| 2014 |
Nielsen MC, Bonney KJ, Schoenebeck F. Computational ligand design for the reductive elimination of ArCF₃ from a small bite angle Pd(II) complex: remarkable effect of a perfluoroalkyl phosphine. Angewandte Chemie (International Ed. in English). 53: 5903-6. PMID 24840791 DOI: 10.1002/Anie.201400837 |
0.831 |
|
| 2014 |
Bonney KJ, Schoenebeck F. Experiment and computation: a combined approach to study the reactivity of palladium complexes in oxidation states 0 to IV. Chemical Society Reviews. 43: 6609-38. PMID 24759955 DOI: 10.1039/C4Cs00061G |
0.851 |
|
| 2014 |
Lyngvi E, Sanhueza IA, Schoenebeck F. Dispersion Makes the Difference: Bisligated Transition States Found for the Oxidative Addition of Pd(PtBu3)2 to Ar-OSO2R and Dispersion-Controlled Chemoselectivity in Reactions with Pd[P(iPr)(tBu2)]2 Organometallics. 34: 805-812. DOI: 10.1021/Om501199T |
0.833 |
|
| 2014 |
Proutiere F, Lyngvi E, Aufiero M, Sanhueza IA, Schoenebeck F. Combining the Reactivity Properties of PCy3 and PtBu3 into a Single Ligand, P(iPr)(tBu)2. Reaction via Mono- or Bisphosphine Palladium(0) Centers and Palladium(I) Dimer Formation Organometallics. 33: 6879-6884. DOI: 10.1021/Om5009605 |
0.792 |
|
| 2014 |
Chiu M, Tchitchanov BH, Zimmerli D, Sanhueza IA, Schoenebeck F, Trapp N, Schweizer WB, Diederich F. Spannungsvermittelte Bildung chiraler, optisch aktiver Buta-1,3-diene Angewandte Chemie. 127: 356-361. DOI: 10.1002/Ange.201409289 |
0.698 |
|
| 2013 |
Sanhueza IA, Bonney KJ, Nielsen MC, Schoenebeck F. Trifluoromethylation of ketones and aldehydes with Bu₃SnCF₃. The Journal of Organic Chemistry. 78: 7749-53. PMID 23834264 DOI: 10.1021/Jo401099E |
0.75 |
|
| 2013 |
Nielsen MC, Lyngvi E, Schoenebeck F. Chemoselectivity in the reductive elimination from high oxidation state palladium complexes--scrambling mechanism uncovered. Journal of the American Chemical Society. 135: 1978-85. PMID 23316762 DOI: 10.1021/Ja312047B |
0.85 |
|
| 2013 |
Bonney KJ, Proutiere F, Schoenebeck F. Dinuclear Pd(i) complexes—solely precatalysts? Demonstration of direct reactivity of a Pd(i) dimer with an aryl iodide Chemical Science. 4: 4434. DOI: 10.1039/C3Sc52054D |
0.838 |
|
| 2013 |
Sanhueza IA, Wagner AM, Sanford MS, Schoenebeck F. On the role of anionic ligands in the site-selectivity of oxidative C-H functionalization reactions of arenes Chemical Science. 4: 2767-2775. DOI: 10.1039/C3Sc00017F |
0.78 |
|
| 2013 |
Lyngvi E, Schoenebeck F. Oxidative addition transition states of Pd(0) complexes in polar solvent—a DFT study involving implicit and explicit solvation Tetrahedron. 69: 5715-5718. DOI: 10.1016/J.Tet.2013.03.095 |
0.825 |
|
| 2013 |
Sanhueza IA, Nielsen MC, Ottiger M, Schoenebeck F. ChemInform Abstract: CuI-Mediated Trifluoromethylations with Stannanes. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201317052 |
0.686 |
|
| 2012 |
Lyngvi E, Bode JW, Schoenebeck F. A Computational Study of the Origin of Stereoinduction in NHC-Catalyzed Annulation Reactions of α,β-Unsaturated Acyl Azoliums. Chemical Science (Royal Society of Chemistry : 2010). 3: 2346-2350. PMID 23687566 DOI: 10.1039/C2Sc20331F |
0.788 |
|
| 2012 |
Zhou L, Li Z, Zou Y, Wang Q, Sanhueza IA, Schoenebeck F, Goeke A. Tandem nucleophilic addition/oxy-2-azonia-Cope rearrangement for the formation of homoallylic amides and lactams: total synthesis and structural verification of motuporamine G. Journal of the American Chemical Society. 134: 20009-12. PMID 23181450 DOI: 10.1021/Ja310002M |
0.729 |
|
| 2012 |
Aufiero M, Proutiere F, Schoenebeck F. Redox reactions in palladium catalysis: on the accelerating and/or inhibiting effects of copper and silver salt additives in cross-coupling chemistry involving electron-rich phosphine ligands. Angewandte Chemie (International Ed. in English). 51: 7226-30. PMID 22689543 DOI: 10.1002/Anie.201202504 |
0.83 |
|
| 2012 |
Zou Y, Ding C, Zhou L, Li Z, Wang Q, Schoenebeck F, Goeke A. Tandem cross-dimerisation/oxonia-cope reaction of carbonyl compounds to homoallylic esters and lactones. Angewandte Chemie (International Ed. in English). 51: 5647-51. PMID 22539267 DOI: 10.1002/Anie.201200425 |
0.304 |
|
| 2012 |
Cahard E, Schoenebeck F, Garnier J, Cutulic SP, Zhou S, Murphy JA. Electron transfer to benzenes by photoactivated neutral organic electron donor molecules. Angewandte Chemie (International Ed. in English). 51: 3673-6. PMID 22389276 DOI: 10.1002/Anie.201200084 |
0.448 |
|
| 2012 |
Proutiere F, Aufiero M, Schoenebeck F. Reactivity and stability of dinuclear Pd(I) complexes: studies on the active catalytic species, insights into precatalyst activation and deactivation, and application in highly selective cross-coupling reactions. Journal of the American Chemical Society. 134: 606-12. PMID 22132686 DOI: 10.1021/Ja209424Z |
0.844 |
|
| 2012 |
Schoenebeck F, Proutiere F. Orthogonal Selectivities under Pd(0) Catalysis with Solvent Polarity: An Interplay of Computational and Experimental Studies Synlett. 23: 645-648. DOI: 10.1055/S-0031-1290564 |
0.845 |
|
| 2012 |
Lyngvi E, Bode JW, Schoenebeck F. A computational study of the origin of stereoinduction in NHC-catalyzed annulation reactions of α,β-unsaturated acyl azoliums Chemical Science. 3: 2346-2350. DOI: 10.1039/c2sc20331f |
0.772 |
|
| 2012 |
Sanhueza IA, Nielsen MC, Ottiger M, Schoenebeck F. CuI-Mediated Trifluoromethylations with Stannanes. Preliminary Communication Helvetica Chimica Acta. 95: 2231-2236. DOI: 10.1002/Hlca.201200450 |
0.729 |
|
| 2012 |
Proutiere F, Schoenebeck F. ChemInform Abstract: Orthogonal Selectivities under Pd(0) Catalysis with Solvent Polarity: An Interplay of Computational and Experimental Studies Cheminform. 43: no-no. DOI: 10.1002/chin.201222245 |
0.838 |
|
| 2011 |
Anstaett P, Schoenebeck F. Reductive elimination of ArCF3 from bidentate Pd(II) complexes: a computational study. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 12340-12346. PMID 21928289 DOI: 10.1002/Chem.201101373 |
0.503 |
|
| 2011 |
Proutiere F, Schoenebeck F. Solvent effect on palladium-catalyzed cross-coupling reactions and implications on the active catalytic species. Angewandte Chemie (International Ed. in English). 50: 8192-5. PMID 21751309 DOI: 10.1002/Anie.201101746 |
0.841 |
|
| 2011 |
Proutiere F, Schoenebeck F. Mediumeffekte in Palladium-katalysierten Kreuzkupplungen und Implikationen bezüglich der katalytisch aktiven Spezies Angewandte Chemie. 123: 8342-8345. DOI: 10.1002/Ange.201101746 |
0.801 |
|
| 2010 |
Findlay NJ, Park SR, Schoenebeck F, Cahard E, Zhou SZ, Berlouis LE, Spicer MD, Tuttle T, Murphy JA. Reductions of challenging organic substrates by a nickel complex of a noninnocent crown carbene ligand. Journal of the American Chemical Society. 132: 15462-4. PMID 20961105 DOI: 10.1021/Ja107703N |
0.515 |
|
| 2010 |
Um JM, Gutierrez O, Schoenebeck F, Houk KN, Macmillan DWC. Nature of intermediates in organo-somo catalysis of α-arylation of aldehydes Journal of the American Chemical Society. 132: 6001-6005. PMID 20387888 DOI: 10.1021/Ja9063074 |
0.332 |
|
| 2010 |
Schoenebeck F, Houk KN. Ligand-controlled regioselectivity in palladium-catalyzed cross coupling reactions. Journal of the American Chemical Society. 132: 2496-7. PMID 20121156 DOI: 10.1021/Ja9077528 |
0.582 |
|
| 2009 |
Schoenebeck F, Ess DH, Jones GO, Houk KN. Reactivity and regioselectivity in 1,3-dipolar cycloadditions of azides to strained alkynes and alkenes: a computational study. Journal of the American Chemical Society. 131: 8121-33. PMID 19459632 DOI: 10.1021/Ja9003624 |
0.307 |
|
| 2009 |
Murphy JA, Schoenebeck F, Findlay NJ, Thomson DW, Zhou SZ, Garnier J. One-carbon extrusion from a tetraazafulvalene. Isolation of aldehydes and a study of their origin. Journal of the American Chemical Society. 131: 6475-9. PMID 19415936 DOI: 10.1021/Ja8092746 |
0.526 |
|
| 2009 |
Garcia Y, Schoenebeck F, Legault CY, Merlic CA, Houk KN. Theoretical bond dissociation energies of halo-heterocycles: trends and relationships to regioselectivity in palladium-catalyzed cross-coupling reactions. Journal of the American Chemical Society. 131: 6632-9. PMID 19368385 DOI: 10.1021/Ja9004927 |
0.333 |
|
| 2009 |
Schoenebeck F, Houk KN. Theoretical study of the catalysis of cyanohydrin formation by the cyclic dipeptide catalyst cyclo[(S)-His-(S)-Phe]. The Journal of Organic Chemistry. 74: 1464-72. PMID 19161315 DOI: 10.1021/Jo801958R |
0.352 |
|
| 2008 |
Murphy JA, Garnier J, Park SR, Schoenebeck F, Zhou SZ, Turner AT. Super-electron donors: bis-pyridinylidene formation by base treatment of pyridinium salts. Organic Letters. 10: 1227-30. PMID 18288858 DOI: 10.1021/Ol800134G |
0.491 |
|
| 2007 |
Schoenebeck F, Murphy JA, Zhou SZ, Uenoyama Y, Miclo Y, Tuttle T. Reductive cleavage of sulfones and sulfonamides by a neutral organic super-electron-donor (S.E.D.) reagent. Journal of the American Chemical Society. 129: 13368-9. PMID 17939662 DOI: 10.1021/Ja074417H |
0.45 |
|
| 2007 |
Murphy JA, Zhou SZ, Thomson DW, Schoenebeck F, Mahesh M, Park SR, Tuttle T, Berlouis LE. The generation of aryl anions by double electron transfer to aryl iodides from a neutral ground-state organic super-electron donor. Angewandte Chemie (International Ed. in English). 46: 5178-83. PMID 17546715 DOI: 10.1002/Anie.200700554 |
0.492 |
|
| 2005 |
Lang S, Corr M, Muir N, Khan TA, Schoenebeck F, Murphy JA, Payne AH, Williams AC. First Organophosphorus Radical-Mediated Cyclizations to Afford Medium-Sized Rings: Eight-Membered Lactones and Seven- and Eight-Membered Lactams. Cheminform. 36. DOI: 10.1016/J.Tetlet.2005.04.032 |
0.425 |
|
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