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MARC Record from marc_columbia

Record ID marc_columbia/Columbia-extract-20221130-031.mrc:39269947:5584
Source marc_columbia
Download Link /show-records/marc_columbia/Columbia-extract-20221130-031.mrc:39269947:5584?format=raw

LEADER: 05584cam a2200637 a 4500
001 15069738
005 20220423231145.0
006 m o d
007 cr cnu---unuuu
008 070516s2006 flua obf 001 0 eng d
035 $a(OCoLC)ocn128110480
035 $a(NNC)15069738
040 $aN$T$beng$epn$cN$T$dOCLCQ$dCUSER$dIDEBK$dE7B$dOCLCQ$dTULIB$dOCLCQ$dOCLCF$dCRCPR$dOCLCQ$dYDXCP$dOCL$dMND$dOCLCQ$dEBLCP$dUAB$dOCLCQ$dNLC$dOCLCQ$dNLE$dCOO$dUKMGB$dWYU$dLEAUB$dUKAHL$dOCLCQ$dVT2$dOCLCQ$dOCLCO$dINARC$dOCLCA$dZCU$dOCLCO$dOCLCQ
015 $aGBB7C7419$2bnb
016 $a(AMICUS)000037826555
016 7 $a018428951$2Uk
019 $a154805162$a173514585$a327018084$a648165554$a779917527$a936818653$a1064922054$a1065700826$a1077293820$a1084437797$a1149371553
020 $a9781420027303$q(electronic bk.)
020 $a1420027301$q(electronic bk.)
020 $a9781574446647
020 $a1574446649
020 $z1574446649$q(acid-free paper)
035 $a(OCoLC)128110480$z(OCoLC)154805162$z(OCoLC)173514585$z(OCoLC)327018084$z(OCoLC)648165554$z(OCoLC)779917527$z(OCoLC)936818653$z(OCoLC)1064922054$z(OCoLC)1065700826$z(OCoLC)1077293820$z(OCoLC)1084437797$z(OCoLC)1149371553
037 $aTANDF_185987$bIngram Content Group
050 4 $aTP201$b.H26 2006eb
072 7 $aTEC$x009010$2bisacsh
082 04 $a661/.8$222
049 $aZCUA
245 00 $aHandbook of chiral chemicals /$cedited by David Ager.
250 $a2nd ed.
260 $aBoca Raton :$bTaylor & Francis,$c2006.
300 $a1 online resource (648 pages) :$billustrations
336 $atext$btxt$2rdacontent
337 $acomputer$bc$2rdamedia
338 $aonline resource$bcr$2rdacarrier
504 $aIncludes bibliographical references and index.
588 0 $aPrint version record.
505 0 $aFront cover; Contents; Preface; The Editor; Contributors; Chapter 1. Introduction; Chapter 2. Amino Acids; Chapter 3. Microbial Pathway Engineering for Amino Acid Manufacture; Chapter 4. Carbohydrates in Synthesis; Chapter 5. Terpenes: The Expansion of the Chiral Pool; Chapter 6. Resolutions at Large Scale: Case Studies; Chapter 7. New Developments in Crystallization-Induced Resolution; Chapter 8. The Role of cis-1-Amino-2-Indanol in Resolution Processes; Chapter 9. Asymmetric Oxidations; Chapter 10. Asymmetric Epoxidation of Olefins by Chiral Ketones.
505 8 $aChapter 11. Ozonolysis in the Production of Chiral Fine ChemicalsChapter 12. Transition Metal Catalyzed Hydrogenations, Isomerizations, and Other Reactions; Chapter 13. Modular, Chiral P-Heterocycles in Asymmetric Catalysis; Chapter 14. Asymmetric Olefin Hydrogenation Using Monodentate BINOL- and Bisphenol-Based Ligands: Phosphonites, Phosphites, and Phosphoramidites; Chapter 15. Asymmetric Catalytic Hydrogenation Reactions with Ferrocene-Based Diphosphine Ligands; Chapter 16. Asymmetric Reduction of Prochiral Ketones Catalyzed by Oxazaborolidines.
505 8 $aChapter 17.-1-Amino-2-Indanol- Derived Ligands in Asymmetric CatalysisChapter 18. Enantioselective Hydrogenation of Activated Ketones Using Heterogeneous Pt Catalysts Modified with Cinchona Alkaloids; Chapter 19. Biotransformations: "Green" Processes for the Synthesis of Chiral Fine Chemicals; Chapter 20. Combining Enzyme Discovery and Evolution to Develop Biocatalysts; Chapter 21. One-Pot Synthesis and the Integration of Chemical and Biocatalytic Conversions; Chapter 22. Substitution Reactions; Chapter 23. Industrial Applications of Chiral Auxiliaries.
505 8 $aChapter 24. The Role and Importance of cis-1-Amino-2-Indanol in Biological Systems and Asymmetric ProcessesChapter 25. Enantiopure Amines by Chirality Transfer Using (R)-Phenylglycine Amide; Chapter 26. Pericyclic Reactions; Chapter 27. Asymmetric Free-Radical Reductions Mediated by Chiral Stannanes, Germanes, and Silanes; Chapter 28. Metathesis Reactions; Chapter 29. Synthesis of Homochiral Compounds: A Small Company's Role*; Chapter 30. Commercial Synthesis of the Antiglaucoma Prostanoid Travoprost; Chapter 31. Synthesis of Large Volume Products; Back cover.
520 $aAs pharmaceutical companies look to develop single enantiomers as drug candidates, chemists are increasingly faced with the problems associated with this subclass of organic synthesis. ""The Handbook of Chiral Chemicals, Second Edition"" highlights the problems associated with the production of chiral compounds on a commercial scale. The handbook first elaborates upon starting materials obtained from a 'chiral pool', which can be derived from natural products. Then it explains methods and reactions that can introduce or influence stereogenic centers, particularly asymmetric hydrogenations, oxi.
650 0 $aChemicals$vHandbooks, manuals, etc.
650 0 $aEnantiomers$vHandbooks, manuals, etc.
650 6 $aProduits chimiques$vGuides, manuels, etc.
650 6 $aÉnantiomères$vGuides, manuels, etc.
650 7 $aTECHNOLOGY & ENGINEERING$xChemical & Biochemical.$2bisacsh
650 7 $aChemicals.$2fast$0(OCoLC)fst00853273
650 7 $aEnantiomers.$2fast$0(OCoLC)fst00909487
655 4 $aElectronic books.
655 7 $aHandbooks and manuals.$2fast$0(OCoLC)fst01423877
655 7 $aHandbooks and manuals.$2lcgft
700 1 $aAger, David J.
776 08 $iPrint version:$tHandbook of chiral chemicals.$b2nd ed.$dBoca Raton : Taylor & Francis, 2006$z1574446649$z9781574446647$w(DLC) 2005043716$w(OCoLC)58545988
856 40 $uhttp://www.columbia.edu/cgi-bin/cul/resolve?clio15069738$zTaylor & Francis eBooks
852 8 $blweb$hEBOOKS