The Palladium Catalysed Suzuki Coupling of 2- and 4-Chloropyridines von Lohse, Olivier

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A new synthesis of oxcarbazepine using a Friedel–Crafts cyclization strategy von Kaufmann, Daniel, Fünfschilling, Peter C., Beutler, Ulrich, Hoehn, Pascale, Lohse, Olivier, Zaugg, Werner

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A New Industrial Process for Oxcarbazepine von Fuenfschilling, Peter C, Zaugg, Werner, Beutler, Ulrich, Kaufmann, Daniel, Lohse, Olivier, Mutz, Jean-Paul, Onken, Ulrich, Reber, Jean-Louis, Shenton, David

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New synthesis of oxcarbazepine via remote metalation of protected N- o-tolyl-anthranilamide derivatives von Lohse, Olivier, Beutler, Ulrich, Fünfschilling, Peter, Furet, Pascal, France †, Julien, Kaufmann, Daniel, Penn, Gerhard, Zaugg, Werner

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An Efficient and Economical Synthesis of 5,6-Diethyl-2,3-dihydro-1 H -inden-2-amine Hydrochloride von Prashad, Mahavir, Hu, Bin, Har, Denis, Repič, Oljan, Blacklock, Thomas J., Lohse, Olivier

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Enantioselective synthesis of (+)-brefeldin A von Solladie, Guy, Lohse, Olivier

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Erratum to “A new synthesis of oxcarbazepine using a Friedel–Crafts cyclization strategy” [Tetrahedron Lett. 45 (2004) 5275] von Kaufmann, Daniel, Fünfschilling, Peter C., Beutler, Ulrich, Hoehn, Pascale, Lohse, Olivier, Zaugg, Werner

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Improved Large-Scale Preparation of 4-Iodopicolinic Acid von Lohse, Olivier

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An Efficient and Economical Synthesis of 5,6-Diethyl-2,3-dihydro-1H-inden-2-amine Hydrochloride von Prashad, Mahavir, Hu, Bin, Har, Denis, Repič, Oljan, Blacklock, Thomas J, Lohse, Olivier

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A Locally Active Antiinflammatory Macrolide (MLD987) for Inhalation Therapy of Asthma von Hersperger, Rene, Buchheit, Karl-Heinz, Cammisuli, Salvatore, Enz, Albert, Lohse, Olivier, Ponelle, Monique, Schuler, Walter, Schweitzer, Alain, Walker, Christoph, Zehender, Hartmut, Zenke, Gerhard, Zimmerlin, Alfred G, Zollinger, Markus, Mazzoni, Lazzaro, Fozard, John R

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Efficient Preparation of (R)- and (S)-2-Amino-1-phenylethanol von Lohse, Olivier, Spöndlin, Christoph

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PROCESS FOR PREPARING 5-[(R)-2-(5,6-DIETHYL-INDAN-2-YLAMINO)-1-HYDROXY-ETHYL]-8-HYDROXY-(1H)-QUINOLIN-2-ONE SALTS, USEFUL AS ADRENOCEPTOR AGONISTS von OLIVIER LOHSE

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PROCESS FOR PREPARING 5-[(R)-2-(5,6-DIETHYL-INDIAN-2-YLAMINO)-1-HYDROXY-ETHYL]-8-HYDROXY-(1H)-QUINOLIN-2-ONE SALT, USEFUL AS AN ADRENOCEPTOR AGONIST von LOHSE OLIVIER, VOGEL CASPAR

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Application of centrifugal counter-current chromatography to the separation of macrolide antibiotic analogues von Wang-Fan, Weizheng, Küsters, Ernst, Lohse, Olivier, Mak, Ching-Pong, Wang, Ying

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derivados de quinazolina, e composição farmacêutica von JEAN-LOUIS REBER, Olivier Lohse, Stéphanie Monnier

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PROCESS FOR PREPARING 5-[(R)-2-(5,6-DIETHYL-INDAN-2-YLAMINO)-1-HYDROXY-ETHYL]-8-HYDROXY-(1H)-QUINOLIN-2-ONE SALT, USEFUL AS AN ADRENOCEPTOR AGONIST von LOHSE, OLIVIER, VOGEL, CASPAR

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Application of centrifugal counter-current chromatography to the separation of macrolide antibiotic analogues: I. Selection of solvent systems based on solubility and partition coe... von Wang-Fan, Weizheng, Küsters, Ernst, Lohse, Olivier, Mak, Ching-Pong, Wang, Ying

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A PROCESS FOR PREPARING 5-[(R)-2-(5,6-DIETHYL-INDAN-2-YLAMINO)-1-HYDROXY-ETHYL]-8-HYDROXY-(1H)-QUINOLIN-2-ONE SALTS, USEFUL AS ADRENORECEPTOR AGONISTS von CASPAR VOGEL, OLIVIER LOHSE

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ENANTIOSELECTIVE PREPARATION OF QUINOLINE DERIVATIVES von CASPAR VOGEL, OLIVIER LOHSE

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processo para preparação de sal de 5-[(r)-2-(5,6-dietil-indan-2-ilamino) -1-hidróxi-etil]-8-hidróxi-(1h)-quinolin-2-ona, intermediários, bem como sal assim obtido von CASPAR VOGEL, OLIVIER LOHSE

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