22 research outputs found

    A New Preparation of 4-Aminobutyramide

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    Kleemann A, Leuchtenberger W, Martens J, Weigel H. A New Preparation of 4-Aminobutyramide. Angew. Chem. Int.Ed. Engl. 1980;19(8):627-627

    Ein neuer Weg zu 4-Amino-buttersäureamid

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    Kleemann A, Leuchtenberger W, Martens J, Weigel H. Ein neuer Weg zu 4-Amino-buttersäureamid. Angew. Chem. 1980;92(8):640-640

    A novel synthetic route to L-proline (Amino acids ; 7)

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    Reaction of L-5-oxoproline esters L-2 with phosgene at 0° C gives L-5,51-dichloro-1-(chlorocarbonyl)proliene esters L-6 ,which readily lose hydrogen chloride to form L-5-chloro-1-(chloroarbonyl)-4,5-dehydroproline esters L-7. Catalytic hydrogenation (Pd/C, 180 bar) of L-7 yields L-1-(chlorocarbonyl)proline esters L-15 and thence, upon hydrolysis, L-proline ( L17 ). A "one-pot reaction" for the whole sequence is described, starting from easily accessible L-5-oxoproline esters and yielding L-proline in 78% overall yield and 99.7% optical purity

    Amino Acids

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    Drauz K, Grayson I, Kleemann A, Krimmer H-P, Leuchtenberger W, Weckbecker C. Amino Acids. In: Ullmann's encyclopedia of industrial chemistry. Vol 1. Weinheim: Wiley‐VCH Verlag GmbH & Co. KGaA; 2007
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