Organic synthesis [[electronic resource] ] : state of the art 2007-2009 / / Douglass F. Taber

• Record Nr.: UNINA9910461356803321
• Autore: Taber D. F (Douglass F.), <1948->
• Pubbl/distr/stampa: Oxford ; ; New York, : Oxford University Press, 2011
• ISBN: 0-19-756309-0; 1-283-23231-6; 9786613232311; 0-19-984239-6
• Descrizione fisica: 1 online resource (253 p.)
• Collana: Oxford scholarship online
• Disciplina: 547/.2
• Soggetti: Organic compounds - Synthesis - Research; Electronic books.
• Lingua di pubblicazione: Inglese
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Note generali: Previously issued in print: 2011.
• Nota di bibliografia: Includes bibliographical references and indexes.
• Nota di contenuto: 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 Groups; 10. 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; 19. 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 Amines; 33. 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; 42. Practical Enantioselective Construction of Arrays of Stereogenic Centers: The Jørgensen Synthesis of the Autoregulator IM-2
• Sommario/riassunto: Organic 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.