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Josep Cornella - Publications

Affiliations: 
Max Planck Institute for Coal Research, Mülheim an der Ruhr, Nordrhein-Westfalen, Germany 
Area:
Catalysis
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53 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Tsuruta T, Spinnato D, Moon HW, Leutzsch M, Cornella J. Bi-Catalyzed Trifluoromethylation of C(sp)-H Bonds under Light. Journal of the American Chemical Society. PMID 37963280 DOI: 10.1021/jacs.3c10333  0.327
2023 Yang X, Kuziola J, Béland VA, Busch J, Leutzsch M, Burés J, Cornella J. Bismuth-Catalyzed Amide Reduction. Angewandte Chemie (International Ed. in English). e202306447. PMID 37283567 DOI: 10.1002/anie.202306447  0.33
2023 Mato M, Spinnato D, Leutzsch M, Moon HW, Reijerse EJ, Cornella J. Bismuth radical catalysis in the activation and coupling of redox-active electrophiles. Nature Chemistry. PMID 37264103 DOI: 10.1038/s41557-023-01229-7  0.405
2023 Ni S, Yan J, Tewari S, Reijerse EJ, Ritter T, Cornella J. Nickel Meets Aryl Thianthrenium Salts: Ni(I)-Catalyzed Halogenation of Arenes. Journal of the American Chemical Society. 145: 9988-9993. PMID 37126771 DOI: 10.1021/jacs.3c02611  0.309
2022 Kraemer Y, Ghiazza C, Ragan AN, Ni S, Lutz S, Neumann EK, Fettinger JC, Nöthling N, Goddard R, Cornella J, Pitts CR. Strain-Release Pentafluorosulfanylation and Tetrafluoro(aryl)sulfanylation of [1.1.1]Propellane: Reactivity and Structural Insight. Angewandte Chemie (International Ed. in English). PMID 36137228 DOI: 10.1002/anie.202211892  0.617
2022 Le Vaillant F, Mateos Calbet A, González-Pelayo S, Reijerse EJ, Ni S, Busch J, Cornella J. Catalytic synthesis of phenols with nitrous oxide. Nature. 604: 677-683. PMID 35478236 DOI: 10.1038/s41586-022-04516-4  0.312
2022 Moon HW, Cornella J. Bismuth Redox Catalysis: An Emerging Main-Group Platform for Organic Synthesis. Acs Catalysis. 12: 1382-1393. PMID 35096470 DOI: 10.1021/acscatal.1c04897  0.315
2021 Ghiazza C, Faber T, Gómez-Palomino A, Cornella J. Deaminative chlorination of aminoheterocycles. Nature Chemistry. 14: 78-84. PMID 34916597 DOI: 10.1038/s41557-021-00812-0  0.328
2021 Magre M, Cornella J. Redox-Neutral Organometallic Elementary Steps at Bismuth: Catalytic Synthesis of Aryl Sulfonyl Fluorides. Journal of the American Chemical Society. 143: 21497-21502. PMID 34914387 DOI: 10.1021/jacs.1c11463  0.435
2021 Pang Y, Leutzsch M, Nöthling N, Katzenburg F, Cornella J. Catalytic Hydrodefluorination via Oxidative Addition, Ligand Metathesis, and Reductive Elimination at Bi(I)/Bi(III) Centers. Journal of the American Chemical Society. PMID 34358426 DOI: 10.1021/jacs.1c06735  0.312
2020 Le Vaillant F, Reijerse EJ, Leutzsch M, Cornella J. Dialkyl Ether Formation at High-Valent Nickel. Journal of the American Chemical Society. 142: 19540-19550. PMID 33143423 DOI: 10.1021/jacs.0c07381  0.347
2020 Wang L, Cornella J. A Unified Strategy for Arylsulfur(VI) Fluorides from Aryl Halides: Access to Ar-SOF3 Compounds. Angewandte Chemie (International Ed. in English). PMID 32940381 DOI: 10.1002/Anie.202009699  0.348
2020 Planas O, Peciukenas V, Cornella J. Bismuth-Catalyzed Oxidative Coupling of Arylboronic Acids with Triflate and Nonaflate Salts. Journal of the American Chemical Society. PMID 32536157 DOI: 10.1021/Jacs.0C05343  0.507
2020 Ma Y, Pang Y, Chabbra S, Reijerse EJ, Schnegg A, Niski J, Leutzsch M, Cornella J. Radical C-N Borylation of Aromatic Amines Enabled by a Pyrylium Reagent. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31994764 DOI: 10.1002/Chem.202000412  0.446
2020 Planas O, Wang F, Leutzsch M, Cornella J. Fluorination of arylboronic esters enabled by bismuth redox catalysis. Science (New York, N.Y.). 367: 313-317. PMID 31949081 DOI: 10.1126/Science.Aaz2258  0.419
2020 Pang Y, Moser D, Cornella J. Pyrylium Salts: Selective Reagents for the Activation of Primary Amino Groups in Organic Synthesis Synthesis. 52: 489-503. DOI: 10.1055/S-0039-1690703  0.44
2020 Nattmann L, Cornella J. Ni(4-tBustb)3: A Robust 16-Electron Ni(0) Olefin Complex for Catalysis Organometallics. DOI: 10.1021/Acs.Organomet.0C00485  0.315
2020 Pérez‐Palau M, Cornella J. Synthesis of Sulfonyl Fluorides from Sulfonamides European Journal of Organic Chemistry. 2020: 2497-2500. DOI: 10.1002/Ejoc.202000022  0.338
2019 Gómez-Palomino A, Cornella J. Selective Late-Stage Sulfonyl Chloride Formation from Sulfonamides Enabled by Pyry-BF. Angewandte Chemie (International Ed. in English). PMID 31595619 DOI: 10.1002/Anie.201910895  0.411
2019 Wang F, Planas O, Cornella J. Bi(I)-Catalyzed Transfer-Hydrogenation with Ammonia-Borane. Journal of the American Chemical Society. PMID 30816708 DOI: 10.1021/Jacs.9B00594  0.362
2019 Ma Y, Cammarata J, Cornella J. Ni-catalyzed Reductive Liebeskind-Srogl Alkylation of Heterocycles. Journal of the American Chemical Society. PMID 30650305 DOI: 10.1021/Jacs.8B13534  0.536
2018 Nattmann L, Lutz S, Ortsack P, Goddard R, Cornella J. A Highly Reduced Ni-Li-Olefin Complex for Catalytic Kumada-Corriu Cross-Couplings. Journal of the American Chemical Society. 140: 13628-13633. PMID 30303378 DOI: 10.1021/Jacs.8B09849  0.474
2018 O'Neill MJ, Cornella J. A Perspective in Catalysis: Development of Efficient Methods in the Age of Sustainability. Chimia. 72: 601-605. PMID 30257734 DOI: 10.2533/Chimia.2018.601  0.35
2018 Moser D, Duan Y, Wang F, Ma Y, O'Neill MJ, Cornella J. Selective Functionalization of Aminoheterocycles by a Pyrylium Salt. Angewandte Chemie (International Ed. in English). PMID 29969531 DOI: 10.1002/Anie.201806271  0.417
2018 O'Neill MJ, Riesebeck T, Cornella J. Catalytic Thorpe-Ingold Effect for Branch-Selective Alkylation of Unactivated Aryl Fluorides. Angewandte Chemie (International Ed. in English). PMID 29786926 DOI: 10.1002/Anie.201804479  0.502
2018 O’Neill M, Cornella J. Retaining Alkyl Nucleophile Regiofidelity in Transition-Metal- Mediated Cross-Couplings to Aryl Electrophiles Synthesis. 50: 3974-3996. DOI: 10.1055/S-0037-1609941  0.464
2017 deGruyter JN, Malins LR, Wimmer L, Clay KJ, Lopez-Ogalla J, Qin T, Cornella J, Liu Z, Che G, Bao D, Stevens JM, Qiao JX, Allen MP, Poss MA, Baran PS. CITU: A Peptide and Decarboxylative Coupling Reagent. Organic Letters. PMID 29115835 DOI: 10.1021/Acs.Orglett.7B03121  0.686
2017 Juliá-Hernández F, Moragas T, Cornella J, Martin R. Remote carboxylation of halogenated aliphatic hydrocarbons with carbon dioxide. Nature. 545: 84-88. PMID 28470192 DOI: 10.1038/Nature22316  0.469
2017 Sandfort F, O'Neill MJ, Cornella J, Wimmer L, Baran PS. Alkyl-(Hetero)Aryl Bond Formation via Decarboxylative Cross-Coupling: A Systematic Analysis. Angewandte Chemie (International Ed. in English). PMID 28185368 DOI: 10.1002/Anie.201612314  0.659
2016 Toriyama F, Cornella J, Wimmer L, Chen TG, Dixon DD, Creech G, Baran PS. Redox-Active Esters in Fe-catalyzed C-C Coupling. Journal of the American Chemical Society. PMID 27548696 DOI: 10.1021/Jacs.6B07172  0.701
2016 Wang J, Qin T, Chen TG, Wimmer L, Edwards JT, Cornella J, Vokits B, Shaw SA, Baran PS. Nickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic Acids. Angewandte Chemie (International Ed. in English). PMID 27380912 DOI: 10.1002/Anie.201605463  0.656
2016 Qin T, Cornella J, Li C, Malins LR, Edwards JT, Kawamura S, Maxwell BD, Eastgate MD, Baran PS. A general alkyl-alkyl cross-coupling enabled by redox-active esters and alkylzinc reagents. Science (New York, N.Y.). PMID 27103669 DOI: 10.1126/Science.Aaf6123  0.721
2016 Cornella J, Edwards JT, Qin T, Kawamura S, Wang J, Pan CM, Gianatassio R, Schmidt MA, Eastgate MD, Baran PS. Practical Ni-Catalyzed Aryl-Alkyl Cross-Coupling of Secondary Redox-Active Esters. Journal of the American Chemical Society. PMID 26835704 DOI: 10.1021/Jacs.6B00250  0.663
2015 Cornella J, Jackson EP, Martin R. Nickel-catalyzed enantioselective C-C bond formation through C(sp2)-O cleavage in aryl esters. Angewandte Chemie (International Ed. in English). 54: 4075-8. PMID 25650559 DOI: 10.1002/Anie.201412051  0.456
2014 Moragas T, Cornella J, Martin R. Ligand-controlled regiodivergent Ni-catalyzed reductive carboxylation of allyl esters with CO2. Journal of the American Chemical Society. 136: 17702-5. PMID 25473825 DOI: 10.1021/Ja509077A  0.371
2014 Grainger R, Cornella J, Blakemore DC, Larrosa I, Campanera JM. The ortho-substituent effect on the Ag-catalysed decarboxylation of benzoic acids. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 16680-7. PMID 25336158 DOI: 10.1002/Chem.201402931  0.353
2014 Cornella J, Zarate C, Martin R. Metal-catalyzed activation of ethers via C-O bond cleavage: a new strategy for molecular diversity. Chemical Society Reviews. 43: 8081-97. PMID 25157613 DOI: 10.1039/C4Cs00206G  0.449
2014 Liu Y, Cornella J, Martin R. Ni-catalyzed carboxylation of unactivated primary alkyl bromides and sulfonates with CO2. Journal of the American Chemical Society. 136: 11212-5. PMID 25068174 DOI: 10.1021/Ja5064586  0.382
2014 Cornella J, Zarate C, Martin R. Ni‐catalyzed Reductive Cleavage of Methyl 3‐Methoxy‐2‐Naphthoate Organic Syntheses. 91: 260-272. DOI: 10.1002/0471264229.Os091.23  0.38
2013 Cornella J, Martin R. Ni-catalyzed stereoselective arylation of inert C-O bonds at low temperatures. Organic Letters. 15: 6298-301. PMID 24252127 DOI: 10.1021/Ol4031815  0.375
2013 Cornella J, Gómez-Bengoa E, Martin R. Combined experimental and theoretical study on the reductive cleavage of inert C-O bonds with silanes: ruling out a classical Ni(0)/Ni(II) catalytic couple and evidence for Ni(I) intermediates. Journal of the American Chemical Society. 135: 1997-2009. PMID 23316793 DOI: 10.1021/Ja311940S  0.445
2013 Correa A, Cornella J, Martin R. Nickel-catalyzed decarbonylative C-H coupling reactions: a strategy for preparing bis(heteroaryl) backbones. Angewandte Chemie (International Ed. in English). 52: 1878-80. PMID 23288859 DOI: 10.1002/Anie.201208843  0.441
2013 Correa A, Cornella J, Martin R. Nickel-katalysierte decarbonylierende C-H-Kupplungen: eine Strategie zur Synthese von Bis(heteroaryl)-Strukturen Angewandte Chemie. 125: 1928-1930. DOI: 10.1002/Ange.201208843  0.332
2012 Grainger R, Nikmal A, Cornella J, Larrosa I. Selective deuteration of (hetero)aromatic compounds via deutero-decarboxylation of carboxylic acids. Organic & Biomolecular Chemistry. 10: 3172-4. PMID 22418863 DOI: 10.1039/C2Ob25157D  0.395
2012 Larrosa I, Cornella J. Decarboxylative Carbon-Carbon Bond-Forming Transformations of (Hetero)aromatic Carboxylic Acids Synthesis. 44: 653-676. DOI: 10.1055/S-0031-1289686  0.327
2011 Cornella J, Righi M, Larrosa I. Carboxylic acids as traceless directing groups for formal meta-selective direct arylation. Angewandte Chemie (International Ed. in English). 50: 9429-32. PMID 21948440 DOI: 10.1002/Anie.201103720  0.356
2011 Cornella J, Rosillo-Lopez M, Larrosa I. A Novel Mode of Reactivity for Gold(I): The Decarboxylative Activation of (Hetero)Aromatic Carboxylic Acids Advanced Synthesis & Catalysis. 353: 1359-1366. DOI: 10.1002/Adsc.201100109  0.423
2010 Cornella J, Lahlali H, Larrosa I. Decarboxylative homocoupling of (hetero)aromatic carboxylic acids. Chemical Communications (Cambridge, England). 46: 8276-8. PMID 20882244 DOI: 10.1039/C0Cc01943G  0.374
2010 Sánchez C, Ariza X, Cornellà J, Farràs J, Garcia J, Ortiz J. Stereodivergent addition of 4-silyloxy-1,2-allenes to aldehydes by hydroboration. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 11535-8. PMID 20806298 DOI: 10.1002/Chem.201001563  0.365
2009 Lu P, Sanchez C, Cornella J, Larrosa I. Silver-catalyzed protodecarboxylation of heteroaromatic carboxylic acids. Organic Letters. 11: 5710-3. PMID 19924891 DOI: 10.1021/Ol902482P  0.401
2009 Cornella J, Sanchez C, Banawa D, Larrosa I. Silver-catalysed protodecarboxylation of ortho-substituted benzoic acids. Chemical Communications (Cambridge, England). 7176-8. PMID 19921021 DOI: 10.1039/B916646G  0.463
2009 Cornella J, Lu P, Larrosa I. Intermolecular decarboxylative direct C-3 arylation of indoles with benzoic acids. Organic Letters. 11: 5506-9. PMID 19877661 DOI: 10.1021/Ol902304N  0.525
2009 Ariza X, Cornellà J, Font-Bardia M, Garcia J, Ortiz J, Sánchez C, Solans X. Stereocontrolled synthesis of highly functionalized quaternary carbon centers: a route to alpha-substituted serines. Angewandte Chemie (International Ed. in English). 48: 4202-5. PMID 19415711 DOI: 10.1002/Anie.200900609  0.355
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