LEADER 01154nam a22002651i 4500 001 991002444989707536 005 20030619132131.0 008 030925s1970 it |||||||||||||||||ita 035 $ab12289796-39ule_inst 035 $aARCHE-033736$9ExL 040 $aBiblioteca Interfacoltà$bita$cA.t.i. Arché s.c.r.l. Pandora Sicilia s.r.l. 082 04$a853 100 1 $aMorawski, Kalikst$0453448 245 13$aIl romanzo storico italiano nell'epoca del Risorgimento /$cKalikst Morawski 260 $aWroclaw [etc.] :$bZaklad Narodowy Imienia Ossolinskich Wydawnictwo Polskiej Akademii Nauk,$c1970 300 $a25 p. ;$c24 cm 440 0$aConferenze ;$v44 500 $aIn testa al front. : Accademia polacca delle scienze, biblioteca e centro di studi a Roma 650 4$aRomanzo storico$xItalia$xSec. 19. 907 $a.b12289796$b02-04-14$c08-10-03 912 $a991002444989707536 945 $aLE002 Ann. 420/044$g1$i2002000142856$lle002$o-$pE0.00$q-$rl$s- $t0$u2$v0$w2$x0$y.i12683371$z08-10-03 996 $aRomanzo storico italiano nell'epoca del Risorgimento$9164250 997 $aUNISALENTO 998 $ale002$b08-10-03$cm$da $e-$fita$git $h3$i1 LEADER 05415nam 2200721 a 450 001 9910790281503321 005 20230801222502.0 010 $a1-118-30786-0 010 $a1-280-59181-1 010 $a9786613621641 010 $a1-118-30785-2 010 $a1-119-94342-6 010 $a1-119-94341-8 035 $a(CKB)2670000000178690 035 $a(EBL)894816 035 $a(OCoLC)782128101 035 $a(SSID)ssj0000658083 035 $a(PQKBManifestationID)11395701 035 $a(PQKBTitleCode)TC0000658083 035 $a(PQKBWorkID)10680915 035 $a(PQKB)11339406 035 $a(DLC) 2012013150 035 $a(MiAaPQ)EBC894816 035 $a(Au-PeEL)EBL894816 035 $a(CaPaEBR)ebr10558692 035 $a(CaONFJC)MIL362164 035 $a(EXLCZ)992670000000178690 100 $a20120329d2012 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aPractical methods for biocatalysis and biotransformations 2$b[electronic resource] /$fedited by John Whittall, Peter W. Sutton 205 $a2 210 $aHoboken $cJohn Wiley & Sons Inc.$d2012 215 $a1 online resource (390 p.) 300 $aDescription based upon print version of record. 311 $a1-119-99139-0 320 $aIncludes bibliographical references and index. 327 $aPRACTICAL METHODS FOR BIOCATALYSIS AND BIOTRANSFORMATIONS 2; Contents; List of Contributors; Abbreviations; 1 Biocatalysis in the Fine Chemical and Pharmaceutical Industries; 1.1 Introduction; 1.2 Biotrans Outsourcing - AstraZeneca; 1.3 Biotrans Trends - Lonza; 1.4 Biocatalysis in the Pharma Environment; 1.5 Industrial Use of Hydrolases; 1.6 Industrial Biooxidation and Reduction; 1.7 Industrial Application of Transaminases - Cambrex; 1.8 Biocatalyst Discovery and Improvement; 1.9 From Pathway Engineering to Synthetic Biology 327 $a1.10 Prioritization of Future Biocatalysis and Synthetic Biology Needs1.11 Concluding Remarks; Acknowledgements; References; 2 Reductive Amination; 2.1 ?-Transaminases - Useful Biocatalysts for Chiral Amine Synthesis; 2.2 Preparative Scale Production of a Bulky-Bulky Chiral Amine Using an Engineered Transaminase; 2.3 Synthesis of Optically Pure Amines Employing ?-Transaminases; 2.4 A Fast, Sensitive Assay and Scale-Up of ?-Transaminase Catalysed Reactions; 2.5 Asymmetric Synthesis of L-3-Hydroxyadamantylglycine Using Branched Chain Aminotransferase 327 $a2.6 Asymmetric Reduction of Aryl Imines Using Candida parapsilosis ATCC 73303 Enoate Reductases for Reduction of Electron Deficient Alkenes; 3.1 Asymmetric Bioreduction of Activated Alkenes Using Ene-Reductases from the Old Yellow Enzyme Family; 3.2 Efficient Baker's Yeast Mediated Reduction with Substrate Feeding Product Removal (SFPR) Technology: Synthesis of (S)-2-Alkoxy-3-Aryl-1-Propanols; 3.3 Asymmetric Reduction of (4S)-(+)-Carvone Catalyzed by Enoate Reductases (ERs) Expressed by Non-Conventional Yeast (NCY) Whole Cells 327 $a3.4 Preparation of Enantiomerically Pure Citronellal Enantiomers Using Alkene Reductases3.5 Highly Enantiomeric Hydrogenation of C-C Double Bond of Methylated N-Phenyl and N-Phenylalkylmaleimides by Aspergillus fumigatus; 4 Industrial Carbonyl Reduction; 4.1 Bioreduction Using Immobilized Carbonyl Reductase Technology; 4.2 Preparative Ketoreductase-Catalyzed Kinetic Resolution of a Racemic Aldehyde; 4.3 Enzymatic Reduction of 2,6-dichloro-3-fluoro-acetophenone to Produce (S)-1-(2,6-dichloro-3-fluorophenyl)ethanol 327 $a4.4 Preparative Scale Production of Poorly Soluble Chiral Alcohol Intermediate for Montelukast5 Regio- and Stereoselective Hydroxylation; 5.1 Engineering of an Amycolatopsis orientalis P450 Compactin Hydroxylase into a Pravastatin Synthase by Changing the Stereospecificity of the Enzyme; 5.2 Recombinant Human Cytochrome P450 Enzymes Expressed in Escherichia coli as Whole Cell Biocatalysts: Preparative Synthesis of Oxidized Metabolites of an mGlu5 Receptor Antagonist; 5.3 Alpha-Keto Biooxidation Using Cunninghamella echinulata (DSM 63356) 327 $a5.4 Aromatic Hydroxylation: Preparation of 3,4-Dihydroxyphenylacetic Acid 330 $aBiocatalysts are increasingly used by chemists engaged in fine chemical synthesis within both industry and academia. Today, there exists a huge choice of high-tech enzymes and whole cell biocatalysts, which add enormously to the repertoire of synthetic possibilities. Practical Methods for Biocatalysis and Biotransformations 2 is a ""how-to"" guide that focuses on the practical applications of enzymes and strains of microorganisms that are readily obtained or derived from culture collections. The sources of starting materials and reagents, hints, tips and safety advice (where appropria 606 $aEnzymes$xBiotechnology 606 $aBiotransformation (Metabolism) 606 $aOrganic compounds$xSynthesis 615 0$aEnzymes$xBiotechnology. 615 0$aBiotransformation (Metabolism) 615 0$aOrganic compounds$xSynthesis. 676 $a572 701 $aWhittall$b John$0855536 701 $aSutton$b Peter$g(Peter W.)$0866821 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910790281503321 996 $aPractical methods for biocatalysis and biotransformations 2$93688899 997 $aUNINA