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Organic synthesis [electronic resource]
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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.
| Title |
Organic synthesis [electronic resource] : state of the art 2007-2009 / Douglass F. Taber. |
|---|---|
| Edition |
1st ed. |
| Publisher |
Oxford New York : Oxford University Press |
| Creation Date |
2011 |
| Notes |
Previously issued in print: 2011. Includes bibliographical references and indexes. English |
| Content |
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 |
| Series |
Oxford scholarship online |
| Extent |
1 online resource (253 p.) |
| Language |
English |
| National Library system number |
997010717305405171 |
MARC RECORDS
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