05060nam 2200661 a 450 991046135680332120200520144314.00-19-756309-01-283-23231-697866132323110-19-984239-6(CKB)2670000000113197(EBL)760039(OCoLC)747410632(SSID)ssj0000539777(PQKBManifestationID)12211357(PQKBTitleCode)TC0000539777(PQKBWorkID)10580992(PQKB)11657683(MiAaPQ)EBC760039(StDuBDS)EDZ0002351212(Au-PeEL)EBL760039(CaPaEBR)ebr10493952(CaONFJC)MIL323231(EXLCZ)99267000000011319720100520d2011 uy 0engur|n|---|||||txtccrOrganic synthesis[electronic resource] state of the art 2007-2009 /Douglass F. TaberOxford ;New York Oxford University Press20111 online resource (253 p.)Oxford scholarship onlinePreviously issued in print: 2011.0-19-976454-9 Includes bibliographical references and indexes.Cover; 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: (-)-β-Conhydrine (Barua) and (+)-6'-Hydroxyarenarol (Anderson); 8. New Methods for Functional Group Conversion; 9. Protection of Organic Functional Groups10. 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 Alkenes19. 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 (Fürstner)28. 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 (Urpí/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 Amines33. 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 Centers42. Practical Enantioselective Construction of Arrays of Stereogenic Centers: The Jørgensen Synthesis of the Autoregulator IM-2Organic 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.Oxford scholarship online.Organic compoundsSynthesisResearchElectronic books.Organic compoundsSynthesisResearch.547/.2Taber D. F(Douglass F.),1948-92850MiAaPQMiAaPQMiAaPQBOOK9910461356803321Organic synthesis1929231UNINA