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Informationen zum Autor Doug Taber is a Professor of Chemistry and Biochemistry at University of Delaware. He is an OUP author of three books in the Organic Synthesis series.Tristan Lambert is an Associate Professor of Chemistry at Columbia University. Klappentext A collection of Douglass Taber's columns originally published between 2013 - 2015 at www.organicchemistry.org Zusammenfassung A collection of Douglass Taber's columns originally published between 2013 - 2015 at www.organicchemistry.org Inhaltsverzeichnis Preface Organic Functional Group Interconversion and Protection 1. Organic Functional Group Interconversion 2. Organic Functional Group Interconversion 3. Organic Functional Group Interconversion 4. Oxidation 5. Functional Group Oxidation and Reduction 6. Oxidation of Organic Functional Groups 7. New Methods for Reduction and for Oxidation 8. Reductions 9. Reduction of Organic Functional Groups 10. Organic Functional Group Protection 11. Organic Functional Group Protection and Deprotection 12. Organic Functional Group Protection 13. Functional Group Protection: The Pohl Synthesis of b-1,4-Mannuronate Oligomers Flow Methods 14. Flow Chemistry: The Direct Production of Drug Metabolites 15. Developments in Flow Chemistry 16. Flow Chemistry C-H Functionalization 17. Selective Functionalization of C-H Bonds 18. C-H Functionalization: The Snyder Synthesis of (+)-Scholarisine A 19. C-H Functionalization: The Maimone Synthesis of Podophyllotoxin 20. C-H Functionalization: The Shaw Synthesis of E-d-Viniferin Carbon-Carbon Bond Construction 21. C-C Bond Construction: The Zhu Synthesis of Goniomitine 22. C-C Bond Construction: The Kingsbury Synthesis of (-)-Dihydrocuscohygrine 23. C-C Bond Construction: The Galano Synthesis of 8-F3t-Isoprostane 24. C-C Bond Construction: The Hou Synthesis of (-)-Brevipolide H Reactions of Alkenes 25. Alkenes 26. Alkene Reactions: The Xu/Loh Synthesis of Vitamin A1 27. Reactions of Alkenes 28. Reactions of Alkenes: The Usami Synthesis of (-)-Pericosine E Enantioselective Construction of Acyclic Stereogenic Centers 29. Construction of Single Stereocenters 30. Enantioselective Synthesis of Alcohols and Amines: The Zhu Synthesis of (+)-Trigonoliimine A 31. Enantioselective Synthesis of Alcohols and Amines: The Kim Synthesis of (+)-Frontalin 32. Enantioselective Synthesis of Alcohols and Amines: The Doi Synthesis of Apratoxin C 33. Construction of Alkylated Stereocenters 34. Enantioselective Construction of Alkylated Centers: The Rawal Synthesis of (+)-Fornicin C 35. Alkylated Stereogenic Centers: The Jia Synthesis of (-)-Goniomitine 36. Construction of Alkylated Stereogenic Centers: The Zhu Synthesis of (-)-Rhazinilam 37. Construction of Multiple Stereocenters 38. Arrays of Stereogenic Centers: The Yadav Synthesis of Nhatrangin A 39. Arrays of Stereogenic Centers: The Thomson Synthesis of (-)-Galcatin 40. Arrays of Stereogenic Centers: The Shin/Chandrasekhar Synthesis of (+)-Lactacystin Construction of C-O Rings 41. C-O Ring Construction. The Martín and Martín Synthesis of Teurilene 42. C-O Ring Formation 43. C-O Ring Construction: The Tong Synthesis of (-)-Aculeatin A 44. C-O Ring Construction: The Smith Synthesis of (+)-18-epi-Latrunculol A 45. C-O Ring Construction: The Oger/Lee/Galano Synthesis of 7(RS)-ST-D8-11-dihomo-Isofuran 46. C-O Ring-Containing Natural Products: Cyanolide A (Krische), Bisabosqual A (Parker), Iso-Eriobrucinol A (Hsung), Trichodermolide A (Hiroya), Batrachotoxin Core (Du Bois) 47. Total Synthesis of C-O Natural Products 48. C-O Natural Products: DihomoIsoF (Lee/Galano), Pyrenolide D (Gracza), Clavilactone A (Li), Psoracorylifol A (Tong), Bermudenynol (Kim), Aspercyclide C (Hirama) 49. C-O Ring Construction: Saur...
