Industrial Applications of the Diels-Alder Reaction von Funel, Jacques-Alexis, Abele, Stefan

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Organic Chemistry: At the Core of Idorsia's Business: A Perspective on Chemistry and Society : A Column on the Occasion of the 75th Anniversary of CHIMIA von Abele, Stefan

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Organic Chemistry: At the Core of Idorsia's Business von Abele, Stefan

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Practical Synthesis of a S1P Receptor 1 Agonist via a Guareschi–Thorpe Reaction von Schmidt, Gunther, Bolli, Martin H, Lescop, Cyrille, Abele, Stefan

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C1-Symmetric Bicyclo[2.2.2]octa-2,5-diene (bod) Ligands in Rhodium-Catalyzed Asymmetric 1,4-Addition of Arylboronic Acids to Enones and 1,2-Addition to N-[(4-Nitrophenyl)sulfonyl]i... von Brönnimann, Rebecca, Chun, Sothys, Marti, Roger, Abele, Stefan

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Catalytic Asymmetric Reduction of a 3,4-Dihydroisoquinoline for the Large-Scale Production of Almorexant: Hydrogenation or Transfer Hydrogenation? von Verzijl, Gerard K. M, de Vries, André H. M, de Vries, Johannes G, Kapitan, Peter, Dax, Thomas, Helms, Matthias, Nazir, Zarghun, Skranc, Wolfgang, Imboden, Christoph, Stichler, Juergen, Ward, Richard A, Abele, Stefan, Lefort, Laurent

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Organic Chemistry: At the Core of Idorsia's Business von Stefan Abele

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Scalable Synthesis of Trifluoromethylated Imidazo-Fused N‑Heterocycles Using TFAA and Trifluoroacetamide as CF3‑Reagents von Schäfer, Gabriel, Ahmetovic, Muhamed, Abele, Stefan

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Metal-Free Amidation of Acids with Formamides and T3P von Bannwart, Linda, Abele, Stefan, Tortoioli, Simone

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One-Pot Synthesis of Trifluoromethylated Quinazolin-4(3H)‑ones with Trifluoroacetic Acid as CF3 Source von Almeida, Sofia, Marti, Roger, Vanoli, Ennio, Abele, Stefan, Tortoioli, Simone

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Robust and Scalable Reductive Amination Protocol for Electron-Poor Heterocyclic Amines Using Et3SiH/TFA as Reducing Agent von Schäfer, Gabriel, Reber, Stefan, Ahmetovic, Muhamed, Fleischer, Tony, Leuenberger, Daniel, Blumer, Nicole, Udry, Megan, Abele, Stefan

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Development of a Scalable, Racemic First-Generation Route for CXCR7 Antagonist ACT-1004-1239 via cis-to-trans Epimerization and Subsequent Separation of Enantiomers von Schäfer, Gabriel, Fleischer, Tony, Ahmetovic, Muhamed, Guerry, Philippe, Abele, Stefan

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Trevor LairdProcess Chemistry Visionary von Abele, Stefan, Pesti, Jaan

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Scalable Synthesis of Trifluoromethylated Imidazo-Fused N-Heterocycles Using TFAA and Trifluoroacetamide as CF 3 -Reagents von Schäfer, Gabriel, Ahmetovic, Muhamed, Abele, Stefan

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Scalable and Practical Synthesis of Halo Quinolin-2(1H)‑ones and Quinolines von Zaugg, Cornelia, Schmidt, Gunther, Abele, Stefan

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Scalable Synthesis of C5aR1 Antagonist ACT-1014-6470 via N 7‑Selective Reductive Amination of an Unprotected Pyrazole Starting Material and Intramolecular Urea Formation with 1,1′-... von Reber, Stefan, Blumer, Nicole, Leuenberger, Daniel, Fleischer, Tony, Renneberg, Dorte, Abele, Stefan, Schäfer, Gabriel

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Scalable Synthesis of Enantiomerically Pure Bicyclo[2.2.2]octadiene Ligands von Abele, Stefan, Inauen, Roman, Spielvogel, Dirk, Moessner, Christian

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Scalable Process for the Production of a Highly Energetic Bromoacetylene Building Block von Kohler, Philipp, Schwaninger, Mischa, Stutz, Alfred, Karge, Reinhard, Abele, Stefan

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One-Pot Synthesis of Trifluoromethylated Quinazolin-4(3 H)-ones with Trifluoroacetic Acid as CF 3 Source von Almeida, Sofia, Marti, Roger, Vanoli, Ennio, Abele, Stefan, Tortoioli, Simone

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Highly Selective Synthesis of 2‑(2H‑1,2,3-Triazol-2-yl)benzoic Acids von Roth, Remo, Schmidt, Gunther, Prud’homme, Alice, Abele, Stefan

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