MARC Record from marc_columbia

LEADER: 05219cam a2200745 i 4500
001 13725811
005 20220430230502.0
006 m o d
007 cr |||||||||||
008 151203s2016 nju ob 001 0 eng
010 $a 2015047720
035 $a(OCoLC)ocn931227028
035 $a(NNC)13725811
040 $aDLC$beng$erda$epn$cDLC$dOCLCF$dN$T$dDG1$dYDXCP$dIDEBK$dOCLCO$dRECBK$dEBLCP$dCOO$dDG1$dUPM$dDG1$dOCLCQ$dDEBSZ$dDKU$dOCLCQ$dKNOVL$dKSU$dCEF$dERL$dUKMGB$dOCLCQ$dLVT$dU3W$dOCLCQ$dERF$dGZM$dOCLCQ$dUWW$dUKAHL$dUKBTH$dOCLCQ$dOCLCO
066 $c(S
015 $aGBB6I2624$2bnb
016 7 $a017945523$2Uk
019 $a950465980$a1036282521$a1086992898
020 $a9781523114740$q(electronic bk.)
020 $a1523114746$q(electronic bk.)
020 $z9781118822357
020 $z1118822358
020 $z9781118822364
020 $z1118822366
020 $z9781118828083
020 $z1118828089
020 $z1118822293
020 $z9781118822296
035 $a(OCoLC)931227028$z(OCoLC)950465980$z(OCoLC)1036282521$z(OCoLC)1086992898
037 $a9781118822364$bWiley
042 $apcc
050 00 $aTP248.65.E59
072 7 $aSCI$x013060$2bisacsh
072 7 $aTEC$x009010$2bisacsh
082 00 $a660$223
084 $aTEC009010$2bisacsh
049 $aZCUA
245 00 $aGreen biocatalysis /$cedited by Ramesh N. Patel.
264 1 $aHoboken, NJ :$bJohn Wiley & Sons,$c2016.
300 $a1 online resource
336 $atext$btxt$2rdacontent
337 $acomputer$bn$2rdamedia
338 $aonline resource$bnc$2rdacarrier
520 $a"This book describes the enzyme-driven syntheses of industrially important compounds and chiral intermediates for chemicals and pharmaceuticals. The chapters describe recent technological advances in enzymatic and microbial transformations and are written by internationally renowned scientists and professors. The synthesis of industrially important molecules is described from the starting substrate to the final product and includes detailed mechanisms. This book addresses the use of various types of reactions catalyzed by microbial cells or enzymes derived from microbes in the production of industrially useful compounds and a variety of drugs. The production of chiral alcohols, amines, unnatural amino acids, esters, carboxylic acids, epoxides, hydroxylated compounds and drug metabolites as well as recent advances in enzyme catalyzed acylation, dehalogenation, esterification, oxidation-reduction, transamination, deamination, C-N, C-C, C-O bond formation, Baeyer-Villegar reaction and aldol as well as acyloin condensation reactions are covered. Cutting-edge topics such as directed evolution by gene shuffling and enzyme engineering to improve biocatalysts will be presented. Enzyme immobilization and reusability studies and enzymatic protection and deprotection are addressed as well"--$cProvided by publisher.
504 $aIncludes bibliographical references and index.
588 0 $aPrint version record and CIP data provided by publisher.
505 0 $6880-01$aTitle Page; Copyright Page; Contents; Preface; About the Editor; Contributors ; Chapter 1 Biocatalysis and Green Chemistry ; 1.1 INTRODUCTION TO SUSTAINABLE DEVELOPMENT AND GREEN CHEMISTRY; 1.2 GREEN CHEMISTRY METRICS; 1.3 ENVIRONMENTAL IMPACT AND SUSTAINABILITY METRICS; 1.4 SOLVENTS; 1.5 THE ROLE OF CATALYSIS; 1.6 BIOCATALYSIS AND GREEN CHEMISTRY; 1.7 EXAMPLES OF GREEN BIOCATALYTIC PROCESSES; 1.7.1 A Chemoenzymatic Process for Pregabalin; 1.7.2 A Three-Enzyme Process for Atorvastatin Intermediate ; 1.7.3 Enzymatic Synthesis of Sitagliptin.
650 0 $aEnzymes$xBiotechnology.
650 0 $aBiocatalysis.
650 0 $aGreen chemistry.
650 2 $aBiocatalysis
650 6 $aEnzymes$xBiotechnologie.
650 6 $aBiocatalyse.
650 6 $aChimie verte.
650 7 $aTECHNOLOGY & ENGINEERING$xChemical & Biochemical.$2bisacsh
650 7 $aBiocatalysis.$2fast$0(OCoLC)fst01896571
650 7 $aEnzymes$xBiotechnology.$2fast$0(OCoLC)fst00913608
650 7 $aGreen chemistry.$2fast$0(OCoLC)fst00912867
655 4 $aElectronic books.
700 1 $aPatel, Ramesh N.,$d1942-
776 08 $iPrint version:$tGreen biocatalysis.$dHoboken, New Jersey : John Wiley & Sons, 2016$z9781118822296$w(DLC) 2015047535
856 40 $uhttp://www.columbia.edu/cgi-bin/cul/resolve?clio13725811.001$zACADEMIC - Biochemistry, Biology & Biotechnology
856 40 $uhttp://www.columbia.edu/cgi-bin/cul/resolve?clio13725811.002$zACADEMIC - Chemistry & Chemical Engineering
880 8 $6505-01/(S$a3.7 INVERSION OF ENANTIOSELECTIVITY DRAMATICALLY IMPROVES CATALYTIC ACTIVITY3.8 FUTURE PROSPECTS; REFERENCES; Chapter 4 Green Processes for the Synthesis of Chiral Intermediates for the Development of Drugs ; 4.1 INTRODUCTION; 4.2 SAXAGLIPTIN: ENZYMATIC SYNTHESIS OF (S)-N-BOC-3-HYDROXYADAMANTYLGLYCINE; 4.3 SITAGLIPTIN: ENZYMATIC SYNTHESIS OF CHIRAL AMINE; 4.4 VANLEV: ENZYMATIC SYNTHESIS OF (S)-6-HYDROXYNORLEUCINE ; 4.5 VANLEV: ENZYMATIC SYNTHESIS OF ALLYSINE ETHYLENE ACETAL; 4.6 VANLEV: ENZYMATIC SYNTHESIS OF THIAZEPINE; 4.7 TIGEMONAM: ENZYMATIC SYNTHESIS OF (S)-β-HYDROXYVALINE.
852 8 $blweb$hEBOOKS