图书简介

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 Martin and Martin 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: Sauropus hexoside (Xie/Wu), (+)-Ipomeamarone (Usuki), Decytospolide A (Fujioka), Cytospolide P (Goswami), (+)-Didemniserinolipid B (Tong), Gymnothelignan N (She); 50. C-O Ring Containing Natural Products: (+)-Isatisine A (Panek), Cephalasporolide E (Sartillo-Piscil), (+)-Xestodecalactone (Jennings), Colchilomycin B (Banwell), Lactimidomycin (Georg), 5,6-Dihydrocineromycin B (Furstner); Construction of C-N Rings; 51. C-N Ring Construction: The Waser Synthesis of Jerantinine E; 52. C-N Ring Construction: The Glorius Synthesis of ent-Monomorine; 53. C-N Ring Construction: The Weinreb Synthesis of Myrioneurinol; 54. C-N Ring Construction: The Hattori Synthesis of (+)-Spectaline; 55. Alkaloid Synthesis: (-)-L-Batzellaside A (Toyooka), Limazepine A (Zemribo), (+)-Febrifugine (Pansare), Amathaspiramide F (Tambar), Allomatrine (Brown), Lyconadine C (Waters), Tabersonine (Andrade); 56. Alkaloid Synthesis: Penaresidin A (Subba Reddy), Allokainic Acid (Saicic), Sedacryptine (Rutjes), Lepistine (Yokoshima/Fukuyama), Septicine (Hanessian), Lyconadin C (Dai); 57. Alkaloid Synthesis: Indolizidine 223AB (Cha), Lepadiformine (Kim), Kainic Acid (Fukuyama), Gephyrotoxin (Smith), Premarineosin A (Reynolds); 58. Alkaloid Synthesis: (-)-a-Kainic Acid (Ohshima), Serpentine (Scheidt), (-)-Galanthamine (Jia), (+)-Trigolutes B (Gong), Sarain A (Yokoshima/Fukuyama), DZ-2384 (Harran); Substituted Benzene Derivatives; 59. Preparation of Benzene Derivatives: The Yu/Baran Synthesis of (+)-Hongoquercin A; 60. Substituted Benzenes: The Garg Synthesis of Tubingensin A; 61. Substituted Benzenes: The Li Synthesis of Rubriflordilactone A; 62. Preparation of Substituted Benzenes: The Beaudry Synthesis of Arundamine; Heteroaromatic Derivatives; 63. Preparation of Heterocycles: The Boukouvalas Synthesis of (-)-Auxofuran; 64. Heteroaromatic Synthesis: The Tokuyama Synthesis of (-)-Rhazinilam; 65. Heteroaromatics: The Zhou/Li Synthesis of Goniomitine; 66. Heteroaromatic Construction: The Li Synthesis of Mycoleptodiscin A; Organocatalyzed C-C Ring Construction; 67. Organocatalyzed C-C Ring Construction: The Carreira Synthesis of (+)-Crotogoudin; 68. Organocatalyzed C-C Ring Construction: The Jorgenson Synthesis of (+)-Estrone; 69. Organocatalyzed C-C Ring Construction: The Bradshaw/Bonjoch Synthesis of (-)-Cermizine B; 70. Organocatalyzed C-C Ring Construction: The Mihovilovic Synthesis of Piperenol B; Metal-Mediated C-C Ring Construction; 71. Metal-mediated C-C Ring Construction: The Carreira Synthesis of (+)-Asperolide C; 72. Metal-Mediated C-C Ring Construction: The Sun/Lin Synthesis of Huperzine A; 73. Metal-Mediated C-C Ring Construction: The Ding Synthesis of (-)-Indoxamycin B; 74. Metal-Mediated C-C Ring Construction: The Lei Synthesis of (-)-Huperzine Q; Intermolecular and Intramolecular Diels-Alder Reactions; 75. Diels-Alder Cycloaddition: Pancratistatin (Cho), Reddy (Nootkatone), Zhang/Lee (Platensimycin), Nakada (Scabronine G), Isoglaziovianol (Trauner); 76. Diels-Alder Cycloaddition: Fawcettimine (Zhai), Sculponeatin N (Zhai), Elansolid B1 (Kirschning), Frondosin A (Wright), Kingianin H (Parker), Rufescenolide (Snyder); 77. Diels-Alder Cycloaddition: Nicolaioidesin B (Coster), Lycorine (Cho), Bucidarasin A (Nakada), Maoecrystal V (Thomson), Kuwanon J (Wulff/Lei), Vinigrol (Kaliappan); 78. Diels-Alder Cycloaddition: Sarcandralactone A (Snyder), Pseudopterosin (-)-G-J aglycone (Paddon-Row/Sherburn), IBIR-22 (Westwood), Muironolide A (Zakarian), Platencin (Banwell), Chatancin (Maimone); Stereocontrolled C-C Ring Construction; 79. Other Methods for C-C Ring Construction: Pinolinone (Bach), Agelastatin A (Batey), Panaginsene (Lee), Salvileucalin D, Salvileucalin C (Ding), ent-Codeine (Hudlicky), Walsucochin B (Xie/Shi); 80. Carbocyclic Ring Construction: The Nicolaou Synthesis of Myceliothermophin E; Classics in Total Synthesis; 81. The Inoue Synthesis of 19-Hydroxysarmentogenin; 82. The Nakada Synthesis of (+)-Ophiobolin A; 83. The Herzon Synthesis of (-)-Acutumine; 84. The Njardarson Synthesis of Vinigrol; 85. The Gin Synthesis of Neofinaconitine; 86. The Li Synthesis of Daphenylline; 87. The Baran Synthesis of Ingenol; 88. The Furstner Synthesis of Amphidinolide F; 89. The Deslongchamps Synthesis of (+)-Cassaine; 90. The Kan Synthesis of the Streptomyces Alkaloid SB-203207; 91. The Trost Synthesis of (-)-Lasonolide A; 92. The Fukuyama Synthesis of (-)-Lepenine; 93. The Smith Synthesis of (-)-Calyciphylline N; 94. The Paterson Synthesis of (-)-Leiodermatolide; 95. The Fuwa Synthesis of Didemnaketal B; 96. The Lee Synthesis of (-)-Crinipellin A; 97. The Snyder Synthesis of Psylloborine A; 98. The Morken Synthesis of (+)-Discodermolide; 99. The Trauner Synthesis of (-)-Nitidasin; 100. The Hoveyda Synthesis of Disorazole C1; 101. The Smith Synthesis of (-)-Nodulisporic Acid D; 102. The Sato/Chida Synthesis of Paclitaxel (TaxolRG); 103. The Johnson Synthesis of Paspaline; 104. The Ding Synthesis of Steenkrotin A

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