{"product_id":"organic-synthesis-state-of-the-art-2003-2005-hardback-9780470053317","title":"Organic Synthesis; State of the Art 2003 - 2005 (Hardback) 9780470053317","description":"\u003cfont face=\"Georgia\"\u003e\r\n\u003cp\u003e\u003cfont size=\"6\"\u003eOrganic Synthesis\u003c\/font\u003e\u003cbr\u003e\r\n\u003cfont size=\"5\"\u003eState of the Art 2003 - 2005\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\r\n\r\n\u003cp\u003e\u003cfont size=\"4\"\u003eDouglass F. Taber (Author)\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e9780470053317, Wiley\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eHardback, published 10 October 2006\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e240 pages\u003cbr\u003e23.6 x 16 x 2 cm, 0.476 kg\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\r\n\u003cp align=\"justify\"\u003e\u003cem\u003e\u003cfont size=\"3\"\u003e\"…an excellent survey of modern synthetic transformations.\" (\u003ci\u003eJournal of Medicinal Chemistry\u003c\/i\u003e, December 28, 2006)  \u003cp\u003e\"...definitely a book to take on a long international flight to catch up on papers you may have missed.\" (\u003ci\u003eOrganic  Process Research and Development Journal,\u003c\/i\u003e July 2007)\u003c\/p\u003e\u003c\/font\u003e\u003c\/em\u003e\u003c\/p\u003e\r\n\r\n\u003cp align=\"justify\"\u003e\u003cstrong\u003e\u003cfont size=\"3\"\u003eThe first in a new series, this book provides chemists an effective, much-needed way to stay abreast of recent developments in organic synthesis. The 103 articles review the leading synthetic procedures developed from 2003 - 2005, discussing their significance and their applications. More than 100 reactions are covered, including Heterocycle Construction by Grubbs Metathesis, Enantioselective C-C Bond Construction, and Organic Reactions in Ionic Liquids.\u003c\/font\u003e\u003c\/strong\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003ePreface. \u003cp\u003e1. Transition metal-mediated reactions in organic synthesis.\u003c\/p\u003e \u003cp\u003e2. Biotransformations in organic synthesis.\u003c\/p\u003e \u003cp\u003e3. Catalytic Enantioselective Synthesis.\u003c\/p\u003e \u003cp\u003e4. Enantioselective Synthesis of Borrelidin.\u003c\/p\u003e \u003cp\u003e5. Enantioselective Ring Construction.\u003c\/p\u003e \u003cp\u003e6. New Routes to Heterocycles.\u003c\/p\u003e \u003cp\u003e7. Total Synthesis of the Galbulimima Alkaloid GB 13.\u003c\/p\u003e \u003cp\u003e8. Total Synthesis of Ingenol.\u003c\/p\u003e \u003cp\u003e9. Best Synthetic Methods: Functional Group Transformations.\u003c\/p\u003e \u003cp\u003e10. New Methods for Carbon-Carbon Bond Formation.\u003c\/p\u003e \u003cp\u003e11. Mini-Review: Organic Reactions in Ionic Liquids.\u003c\/p\u003e \u003cp\u003e12. Adventures in Polycyclic Ring Construction.\u003c\/p\u003e \u003cp\u003e13. Synthesis of the Mesotricyclic Diterpenoids Jatrophatrione and Citlalitrione.\u003c\/p\u003e \u003cp\u003e14. Best Synthetic Methods: Functional Group Transformations.\u003c\/p\u003e \u003cp\u003e15. The Grubbs Reaction in Organic Synthesis.\u003c\/p\u003e \u003cp\u003e16. C-N Ring-Forming Reactions by Transition Metal-Catalyzed Intramolecular Alkene Hydroamination.\u003c\/p\u003e \u003cp\u003e17. Synthesis of (+)-Phomactin A.\u003c\/p\u003e \u003cp\u003e18. Enzymes in Organic Synthesis.\u003c\/p\u003e \u003cp\u003e19. Adventures in Polycarbocyclic Construction.\u003c\/p\u003e \u003cp\u003e20. Construction of Enantiomerically-Pure Heterocycles.\u003c\/p\u003e \u003cp\u003e21. Best Synthetic Methods: Functional Group Transformations.\u003c\/p\u003e \u003cp\u003e22. Synthesis of (+)-4,5-Deoxyneodolabelline.\u003c\/p\u003e \u003cp\u003e23. New Methods for Carbon-Carbon Bond Formation.\u003c\/p\u003e \u003cp\u003e24. Strategies for Enantioselective Synthesis.\u003c\/p\u003e \u003cp\u003e25. Preparation of Cyclic Amines.\u003c\/p\u003e \u003cp\u003e26. Enantioselective Total Synthesis of (+)-Amphidinolide T1.\u003c\/p\u003e \u003cp\u003e27. Stereocontrolled Construction of Carbacycles.\u003c\/p\u003e \u003cp\u003e28. “Organometallic” Coupling without the Metal!\u003c\/p\u003e \u003cp\u003e29. Preparation ofEnantiomerically-PureBuilding Blocks.\u003c\/p\u003e \u003cp\u003e30. Synthesis of (-)-Strychnine.\u003c\/p\u003e \u003cp\u003e31. Pd-Mediated Coupling in Organic Synthesis: Recent Milestones.\u003c\/p\u003e \u003cp\u003e32. Enantioselective C-C Bond Construction: Part One of Three.\u003c\/p\u003e \u003cp\u003e33. Enantioselective C-C Bond Construction: Part Two of Three.\u003c\/p\u003e \u003cp\u003e34. Enantioselective C-C Bond Construction: Part Three of Three.\u003c\/p\u003e \u003cp\u003e35. Synthesis of (-)-Podophyllotoxin.\u003c\/p\u003e \u003cp\u003e36. The Grubbs Reaction in Organic Synthesis: Part One of Three.\u003c\/p\u003e \u003cp\u003e37. The Grubbs Reaction in Organic Synthesis: Part Two of Three.\u003c\/p\u003e \u003cp\u003e38. The Grubbs Reaction in Organic Synthesis: Part Three of Three.\u003c\/p\u003e \u003cp\u003e39. Synthesis of Deacetoxyalcyonin Acetate.\u003c\/p\u003e \u003cp\u003e40. Enantioselective Ring Construction: Part One of Two.\u003c\/p\u003e \u003cp\u003e41. Enantioselective Ring Construction: Part Two of Two.\u003c\/p\u003e \u003cp\u003e42. Alkyne Metathesis in Synthesis: Syntheses of (+)-Ferrugine and Anatoxin-α.\u003c\/p\u003e \u003cp\u003e43. Catalytic Asymmetric Synthesis of Quinine and Quinidine.\u003c\/p\u003e \u003cp\u003e44. Best Synthetic Methods: Oxidation and Reduction.\u003c\/p\u003e \u003cp\u003e45. Best Synthetic Methods: Enantioselective Oxidation and Reduction.\u003c\/p\u003e \u003cp\u003e46. Asymmetric Nucleophilic Epoxidation.\u003c\/p\u003e \u003cp\u003e47. Asymmetric Synthesis of Nitrogen Heterocycles.\u003c\/p\u003e \u003cp\u003e48. Synthesis of Amphidinolide T1.\u003c\/p\u003e \u003cp\u003e49. Enantioselective C-C Bond Construction: Part One of Two.\u003c\/p\u003e \u003cp\u003e50. Enantioselective C-C Bond Construction: Part Two of Two.\u003c\/p\u003e \u003cp\u003e51. Advances in Nitrogen Protection and Deprotection.\u003c\/p\u003e \u003cp\u003e52. Enantioselective Synthesis of (+)-Tricycloclavulone.\u003c\/p\u003e \u003cp\u003e53. Best Methods for C-C Bond Construction: Part One of Three.\u003c\/p\u003e \u003cp\u003e54. Best Methods for C-C Bond Construction: Part Two of Three.\u003c\/p\u003e \u003cp\u003e55. Best Methods for C-C Bond Construction: Part Three of Three.\u003c\/p\u003e \u003cp\u003e56. Formation of Aromatic-Amino and Aromatic-Carbon Bonds.\u003c\/p\u003e \u003cp\u003e57. Synthesis of the Dendrobatid Alkaloid 251F.\u003c\/p\u003e \u003cp\u003e58. Enantioselective Construction of Aldol Products: Part One of Two.\u003c\/p\u003e \u003cp\u003e59. Enantioselective Construction of Aldol Products: Part Two of Two.\u003c\/p\u003e \u003cp\u003e60. Enantioselective α-Functionalization of Carbonyl Compounds.\u003c\/p\u003e \u003cp\u003e61. Synthesis of (-)-Hamigeran B.\u003c\/p\u003e \u003cp\u003e62. Catalytic C-C Bond-Forming Reactions.\u003c\/p\u003e \u003cp\u003e63. Rare Sugars are now Readily Available Chiral Pool Starting Materials.\u003c\/p\u003e \u003cp\u003e64. Alkyne Metathesis in Organic Synthesis.\u003c\/p\u003e \u003cp\u003e65. Total Synthesis of (±)-Sordaricin.\u003c\/p\u003e \u003cp\u003e66. Ru-Mediated Intramolecular Alkene Metathesis: Improved Substrate and Catalyst Design.\u003c\/p\u003e \u003cp\u003e67. Heterocycle Construction by Grubbs Metathesis.\u003c\/p\u003e \u003cp\u003e68. Natural Product Synthesis using Grubbs Metathesis: Lasubine II, Ingenol, and Ophirin B.\u003c\/p\u003e \u003cp\u003e69. Synthesis of (-)-Tetrodotoxin.\u003c\/p\u003e \u003cp\u003e70. Diastereoselective and Enantioselective Construction of Aza- Heterocycles.\u003c\/p\u003e \u003cp\u003e71. Diastereoselective and Enantioselective Construction of Cyclic Ethers.\u003c\/p\u003e \u003cp\u003e72. Synthesis of Heterocyclic Natural Products: (-)-Ephedradine A, (-)-α-Tocopherol, (-)-Lepadin D and (-)-Phenserine.\u003c\/p\u003e \u003cp\u003e73. Protection of N- and O-Functional Groups.\u003c\/p\u003e \u003cp\u003e74. Synthesis of (-)-Norzoanthamine.\u003c\/p\u003e \u003cp\u003e75. Best Synthetic Methods: C-C Bond Formation.\u003c\/p\u003e \u003cp\u003e76. Enantioselective Construction of Single Stereogenic Centers.\u003c\/p\u003e \u003cp\u003e77. Enantioselective Construction of Arrays of Stereogenic Centers.\u003c\/p\u003e \u003cp\u003e78. Synthesis of (-)-Brasilenyne.\u003c\/p\u003e \u003cp\u003e79. Best Synthetic Methods: Functional Group Transformations.\u003c\/p\u003e \u003cp\u003e80. Enantioselective Construction of Oxygenated and Halogenated Secondary Centers.\u003c\/p\u003e \u003cp\u003e81. Enantioselective Construction of Aminated Secondary Centers.\u003c\/p\u003e \u003cp\u003e82. Enantioselective Synthesis of the Polyene Antibiotic Aglycone Rimocidinolide Methyl Ester.\u003c\/p\u003e \u003cp\u003e83. Enantioselective Transformations of Prochiral Rings.\u003c\/p\u003e \u003cp\u003e84. Michael Reactions for Enantioselective Ring Construction.\u003c\/p\u003e \u003cp\u003e85. Enantioselective Ring Construction by Intramolecular C-H Insertion and by Cycloaddition.\u003c\/p\u003e \u003cp\u003e86. Best Synthetic Methods: Construction of Aromatic and Heteroaromatic Rings.\u003c\/p\u003e \u003cp\u003e87. Enantioselective Synthesis of (+)-Epoxomycin.\u003c\/p\u003e \u003cp\u003e88. Best Synthetic Methods: Functionalization of Aromatic and Heteroaromatic Rings.\u003c\/p\u003e \u003cp\u003e89. Best Synthetic Methods: Oxidation.\u003c\/p\u003e \u003cp\u003e90. Enantioselective Allylic Carbon-Carbon Bond Construction.\u003c\/p\u003e \u003cp\u003e91. Synthesis of (+)-Cyanthawigin U.\u003c\/p\u003e \u003cp\u003e92. Catalysts and Strategies for Alkene Metathesis.\u003c\/p\u003e \u003cp\u003e93. N-Heterocycle Construction by Alkene Metathesis.\u003c\/p\u003e \u003cp\u003e94. O-Heterocyclic Construction by Alkene Metathesis.\u003c\/p\u003e \u003cp\u003e95. Alkene Metathesis in total synthesis: Valienamine, Agelastatin and Tonantzitlolone.\u003c\/p\u003e \u003cp\u003e96. Total Synthesis of the Tetracyclines.\u003c\/p\u003e \u003cp\u003e97. Enantioselective Construction of N-Heterocycles.\u003c\/p\u003e \u003cp\u003e98. Stereocontrolled Construction of Cyclic Ethers.\u003c\/p\u003e \u003cp\u003e99. Synthesis of the Proteosome Inhibitors Salinosporamide A, Omuralide and Lactacystin.\u003c\/p\u003e \u003cp\u003e100. Synthesis of (-)-Sordaricin.\u003c\/p\u003e \u003cp\u003e101. Recent Advances in Carbocyclic Ketone Construction.\u003c\/p\u003e \u003cp\u003e102. Stereoselective Construction of Carbocyclic Rings.\u003c\/p\u003e \u003cp\u003e103. Asymmetric Transformation of Prochiral Carbocyclic Rings.\u003c\/p\u003e\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eSubject Areas: Chemistry [\u003ca title=\"See our other books on Chemistry\" href=\"https:\/\/freshlyprintedbooks.co.uk\/search?q=%22Chemistry%20%5BPN%5D%22\"\u003ePN\u003c\/a\u003e]\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\u003c\/font\u003e","brand":"Wiley-Interscience","offers":[{"title":"Brand New","offer_id":52256842547480,"sku":"9780470053317","price":100.89,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0730\/2037\/5320\/files\/9780470053317.jpg?v=1781275204","url":"https:\/\/freshlyprintedbooks.co.uk\/products\/organic-synthesis-state-of-the-art-2003-2005-hardback-9780470053317","provider":"Freshly Printed Books","version":"1.0","type":"link"}