LEADER 05060nam 2200661 a 450 001 9910461356803321 005 20200520144314.0 010 $a0-19-756309-0 010 $a1-283-23231-6 010 $a9786613232311 010 $a0-19-984239-6 035 $a(CKB)2670000000113197 035 $a(EBL)760039 035 $a(OCoLC)747410632 035 $a(SSID)ssj0000539777 035 $a(PQKBManifestationID)12211357 035 $a(PQKBTitleCode)TC0000539777 035 $a(PQKBWorkID)10580992 035 $a(PQKB)11657683 035 $a(MiAaPQ)EBC760039 035 $a(StDuBDS)EDZ0002351212 035 $a(Au-PeEL)EBL760039 035 $a(CaPaEBR)ebr10493952 035 $a(CaONFJC)MIL323231 035 $a(EXLCZ)992670000000113197 100 $a20100520d2011 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aOrganic synthesis$b[electronic resource] $estate of the art 2007-2009 /$fDouglass F. Taber 210 $aOxford ;$aNew York $cOxford University Press$d2011 215 $a1 online resource (253 p.) 225 1 $aOxford scholarship online 300 $aPreviously issued in print: 2011. 311 $a0-19-976454-9 320 $aIncludes bibliographical references and indexes. 327 $aCover; Contents; Preface; Organic Functional Group Interconversion and Protection; 1. Best Synthetic Methods: Oxidation and Reduction; 2. Functional Group Transformations; 3. Best Synthetic Methods: Oxidation; 4. Best Synthetic Methods: Reduction; 5. Best Synthetic Methods: Functional Group Transformation; 6. New Methods for Functional Group Conversion; 7. Organic Functional Group Interconversion: (-)-?-Conhydrine (Barua) and (+)-6'-Hydroxyarenarol (Anderson); 8. New Methods for Functional Group Conversion; 9. Protection of Organic Functional Groups 327 $a10. Best Synthetic Methods: Functional Group Protection11. Functional Group Protection; C-H Functionalization; 12. Intermolecular and Intramolecular C-H Functionalization; 13. C-H Functionalization to Form C-O, C-N, and C-C Bonds; 14. Functionalization of C-H Bonds: The Baran Synthesis of Dihydroxyeudesmane; Carbon-Carbon Bond Construction; 15. New Methods for Carbon-Carbon Bond Construction; 16. Best Synthetic Methods: Carbon-Carbon Bond Construction; 17. C-C Single Bond Construction; 18. Construction of Alkenes, Alkynes and Allenes; Reactions of Alkenes 327 $a19. Reduction, Oxidation and Homologation of Alkenes20. Reactions of Alkenes; 21. Selective Reactions of Alkenes; Alkene and Alkyne Metathesis; 22. Developments in Alkene Metathesis; 23. Developments in Alkene and Alkyne Metathesis; 24. Advances in Alkene and Alkyne Metathesis; 25. Developments in Alkene Metathesis; 26. Alkene Metathesis: Synthesis of Kainic Acid, Pladienolide B and Amphidinolide Y; 27. Alkene and Alkyne Metathesis: Phaseolinic Acid (Selvakumar), Methyl 7-Dihydro-trioxacarcinoside B (Koert), Arglabin (Reiser) and Amphidinolide V (Fu?rstner) 327 $a28. Alkene Metathesis: Synthesis of Panaxytriol (Lee), Isofagomine (Imahori and Takahata), Elatol (Stoltz), 5-F[Sub(2t)]-Isoprostane (Snapper), and Ottelione B (Clive)29. Total Synthesis by Alkene Metathesis: Amphidinolide X (Urpi?/Vilarrasa), Dactylolide (Jennings), Cytotrienin A (Hayashi), Lepadin B (Charette), Blumiolide C (Altmann); Enantioselective Construction of Acyclic Stereogenic Centers; 30. Enantioselective Assembly of Oxygenated Stereogenic Centers; 31. Enantioselective Assembly of Aminated Stereogenic Centers; 32. Enantioselective Preparation of Secondary Alcohols and Amines 327 $a33. Enantioselective Preparation of Alcohols and Amines34. Enantioselective Synthesis of Alcohols and Amines; 35. Enantioselective Assembly of Alkylated Stereogenic Centers; 36. Enantioselective Construction of Alkylated Stereogenic Centers; 37. Enantioselective Construction of Alkylated Centers; 38. Enantioselective Construction of Alkylated Stereogenic Centers; 39. Stereocontrolled Construction of Arrays of Stereogenic Centers; 40. Enantioselective Construction of Arrays of Stereogenic Centers; 41. Stereocontrolled Construction of Arrays of Stereogenic Centers 327 $a42. Practical Enantioselective Construction of Arrays of Stereogenic Centers: The Jørgensen Synthesis of the Autoregulator IM-2 330 8 $aOrganic synthesis is a vibrant and rapidly evolving field; we can now cyclize amines directly onto alkenes. Like the first two books in this series, this reference leads readers quickly to the most important recent developments. 410 0$aOxford scholarship online. 606 $aOrganic compounds$xSynthesis$xResearch 608 $aElectronic books. 615 0$aOrganic compounds$xSynthesis$xResearch. 676 $a547/.2 700 $aTaber$b D. F$g(Douglass F.),$f1948-$092850 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910461356803321 996 $aOrganic synthesis$91929231 997 $aUNINA