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20050510165600.0 |
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031219s2004 enka 001 0 eng |
| 015 |
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|a GBA3-V5200
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|a 3527306315
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|a *UKM*
|c *UKM*
|d CU
|d CStRLIN
|d OrLoB-B
|d UtOrBLW
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| 082 |
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|a 547.1395
|2 21
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| 245 |
0 |
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|a Asymmetric catalysis on industrial scale :
|b challenges, approaches and solutions /
|c edited by H.U. Blaser, E. Schmidt.
|
| 260 |
|
|
|a Weinheim :
|b Wiley-VCH ;
|a Chichester :
|b John Wiley (distributor),
|c c2004.
|
| 300 |
|
|
|a xxvi, 454 p. :
|b ill. ;
|c 25 cm.
|
| 336 |
|
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|a text
|b txt
|2 rdacontent
|0 http://id.loc.gov/vocabulary/contentTypes/txt
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| 337 |
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|a unmediated
|b n
|2 rdamedia
|0 http://id.loc.gov/vocabulary/mediaTypes/n
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| 338 |
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|a volume
|b nc
|2 rdacarrier
|0 http://id.loc.gov/vocabulary/carriers/nc
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| 504 |
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|a Includes bibliographical references and index.
|
| 505 |
0 |
0 |
|t Introduction /
|r Hans-Ulrich Blaser and Elke Schmidt --
|g I.
|t New Processes for Existing Active Compounds --
|g 1.
|t Asymmetric Hydrogenations - The Monsanto L-Dopa Process /
|r William S. Knowles --
|g 2.
|t The Other L-Dopa Process /
|r Rudiger Selke --
|g 3.
|t The Chiral Switch of Metolachlor: The Development of a Large-Scale Enantioselective Catalytic Process /
|r Hans-Ulrich Blaser, Reinhard Hanreich, Hans-Dieter Schneider, Felix Spindler and Beat Steinacher --
|g 4.
|t Enantioselective Hydrogenation: Towards a Large-Scale Total Synthesis of (R,R,R)-[alpha]-Tocopherol /
|r Thomas Netscher, Michelangelo Scalone and Rudolf Schmid --
|g 5.
|t Comparison of Four Technical Syntheses of Ethyl (R)-2-Hydroxy-4-Phenylbutyrate /
|r Hans-Ulrich Blaser, Marco Eissen, Pierre F. Fauquex, Konrad Hungerbuhler, Elke Schmidt, Gottfried Sedelmeier and Martin Studer --
|g 6.
|t Biocatalytic Approaches for the Large-Scale Production of Asymmetric Synthons /
|r Nicholas M. Shaw, Karen T. Robins and Andreas Kiener --
|g 7.
|t 7-Aminocephalosporanic Acid - Chemical Versus Enzymatic Production Process /
|r Thomas Bayer --
|g 8.
|t Methods for the Enantioselective Biocatalytic Production of L-Amino Acids on an Industrial Scale /
|r Harald Groger and Karlheinz Drauz --
|g II.
|t New Catalysts for Existing Active Compounds --
|g 1.
|t The Large-Scale Biocatalytic Synthesis of Enantiopure Cyanohydrins /
|r Peter Poechlauer, Wolfgang Skranc and Marcel Wubbolts --
|g 2.
|t Industrialization Studies of the Jacobsen Hydrolytic Kinetic Resolution of Epichlorohydrin /
|r Larbi Aouni, Karl E. Hemberger, Serge Jasmin, Hocine Kabir, Jay F. Larrow, Isidore Le-Fur, Philippe Morel and Thierry Schlama --
|g 3.
|t Scale-up Studies in Asymmetric Transfer Hydrogenation /
|r John Blacker and Juliette Martin --
|g 4.
|t Practical Applications of Biocatalysis for the Manufacture of Chiral Alcohols such as (R)-1,3-Butanediol by Stereospecific Oxidoreduction /
|r Akinobu Matsuyama and Hiroaki Yamamoto --
|g 5.
|t Production of Chiral C3 and C4 Units via Microbial Resolution of 2,3-Dichloro-1-propanol, 3-Chloro-1,2-propanediol and Related Halohydrins /
|r N. Kasai and T. Suzuki --
|g III.
|t Adaptation of Existing Catalysts for Important Building Blocks --
|g 1.
|t Synthesis of Unnatural Amino Acids /
|r David J. Ager and Scott A. Laneman --
|g 2.
|t The Application of DuPHOS Rhodium(I) Catalysts for Commercial Scale Asymmetric Hydrogenation /
|r Christopher J. Cobley, Nicholas B. Johnson, Ian C. Lennon, Raymond McCague, James A. Ramsden and Antonio Zanotti-Gerosa --
|g 3.
|t Liberties and Constraints in the Development of Asymmetric Hydrogenations on a Technical Scale /
|r John F. McGarrity, Walter Brieden, Rudolf Fuchs, Hans-Peter Mettler, Beat Schmidt and Oleg Werbitzky --
|g 4.
|t Large-Scale Applications of Biocatalysis in the Asymmetric Synthesis of Laboratory Chemicals /
|r Roland Wohlgemuth --
|g IV.
|t Processes for New Chemical Entities (NCE) --
|g 1.
|t Development of an Efficient Synthesis of Chiral 2-Hydroxy Acids /
|r Junhua Tao and Kevin McGee --
|g 2.
|t Factors Influencing the Application of Literature Methods Toward the Preparation of a Chiral trans-Cyclopropane Carboxylic Acid Intermediate During Development of a Melatonin Agonist /
|r Ambarish K. Singh, J. Siva Prasad and Edward J. Delaney --
|g 3.
|t Hetero Diels-Alder-Biocatalysis Approach for the Synthesis of (S)-3-[2-{(Methylsufonyl)oxy}ethoxy]-4-(triphenylmethoxy)-1-butanol Methanesulfonate: Successful Application of an Enzyme Resolution Process /
|r Jean-Claude Caille, Jim Lalonde, Yiming Yao and C. K. Govindan --
|g 4.
|t Multi-Kilo Resolution of XU305, a Key Intermediate to the Platelet Glycoprotein IIb/IIIa Receptor Antagonist Roxifiban via Kinetic and Dynamic Enzymatic Resolution /
|r Jaan A. Pesti and Luigi Anzalone --
|g 5.
|t Protease-Catalyzed Preparation of (S)-2-[(tert-Butylsulfonyl)methyl]-hydrocinnamic Acid for Renin Inhibitor RO0425892 /
|r Beat Wirz, Stephan Doswald, Ernst Kupfer, Wolfgang Wostl, Thomas Weisbrod and Heinrich Estermann --
|g 6.
|t Protease-Catalyzed Preparation of Chiral 2-Isobutyl Succinic Acid Derivatives for Collagenase Inhibitor RO0319790 /
|r Beat Wirz, Milan Soukup, Thomas Weisbrod, Florian Stabler and Rolf Birk --
|g 7.
|t An Innovative Asymmetric Sulfide Oxidation: The Process Development History Behind the New Antiulcer Agent Esomeprazole /
|r Hans-Jurgen Federsel and Magnus Larsson --
|g 8.
|t Development of a Biocatalytic Process for the Resolution of (R)- and (S)-Ethyl-3-amino-4-pentynoate Isomers Using Enzyme Penicillin G Amidohydrolase /
|r Ravindra S. Topgi.
|
| 650 |
|
0 |
|a Enantioselective catalysis.
|0 http://id.loc.gov/authorities/subjects/sh00009610
|
| 650 |
|
0 |
|a Enantioselective catalysis
|x Industrial applications
|v Case studies.
|
| 650 |
|
7 |
|a Enantioselective catalysis.
|2 fast
|0 http://id.worldcat.org/fast/fst00909493
|
| 655 |
|
7 |
|a Case studies.
|2 fast
|0 http://id.worldcat.org/fast/fst01423765
|
| 700 |
1 |
|
|a Blaser, H. U.
|0 http://id.loc.gov/authorities/names/n97030942
|1 http://viaf.org/viaf/32214159
|
| 700 |
1 |
|
|a Schmidt, Elke,
|d 1959-
|q (Elke),
|c Dr.
|0 http://id.loc.gov/authorities/names/nb2003113495
|
| 901 |
|
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|a ToCBNA
|
| 903 |
|
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|a HeVa
|
| 903 |
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|a Hathi
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| 035 |
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|a (OCoLC)52746672
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| 929 |
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|a cat
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f |
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|i 40b4b50d-d678-5396-970c-cf7f5b554623
|s 48f02c80-6558-5395-9d8c-edb9f818ed01
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| 928 |
|
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|t Library of Congress classification
|a TP156.C35A89 2004
|l JCL
|c JCL-Sci
|i 5004901
|
| 927 |
|
|
|t Library of Congress classification
|a TP156.C35A89 2004
|l JCL
|c JCL-Sci
|e MARO
|e CRERAR
|b 65341051
|i 7605247
|
