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Produktbild: Organic Synthesis

Organic Synthesis State of the Art, 2013-2015

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Beschreibung

Produktdetails

Einband

Gebundene Ausgabe

Erscheinungsdatum

01.11.2017

Verlag

Oxford Academic

Seitenzahl

286

Maße (L/B/H)

24/16,1/2 cm

Gewicht

550 g

Sprache

Englisch

ISBN

978-0-19-064616-5

Beschreibung

Produktdetails

Einband

Gebundene Ausgabe

Erscheinungsdatum

01.11.2017

Verlag

Oxford Academic

Seitenzahl

286

Maße (L/B/H)

24/16,1/2 cm

Gewicht

550 g

Sprache

Englisch

ISBN

978-0-19-064616-5

Herstelleradresse

Libri GmbH
Europaallee 1
36244 Bad Hersfeld
DE

Email: gpsr@libri.de

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  • Produktbild: Organic Synthesis

    • 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: 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 (Fürstner)

    • 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 Jørgenson 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 Fürstner 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 (Taxol®)

    • 103. The Johnson Synthesis of Paspaline

    • 104. The Ding Synthesis of Steenkrotin A