Douglass F. Taber, Tristan Lambert

Organic Synthesis (eBook, PDF)

State of the Art, 2013-2015

• Format: PDF

Produktbeschreibung

Organic synthesis is a vibrant and rapidly evolving field; chemists can now cyclize alkenes directly onto enones. Like the first five books in this series, Organic Synthesis: State of the Art 2013-2015 will lead readers quickly to the most important recent developments in a research area. This series offers chemists a way to stay abreast of what's new and exciting in organic synthesis. The cumulative reaction/transformation index of 2013-2015 outlines all significant new organic transformations over the past twelve years. Future volumes will continue to come out every two years. The 2013-2015 volume features the best new methods in subspecialties such as C-O, C-N and C-C ring construction, catalytic asymmetric synthesis, selective C-H functionalization, and enantioselective epoxidation. This text consolidates two years of Douglass Taber's popular weekly online column, "Organic Chemistry Highlights" as featured on the organic-chemistry.org website and also features cumulative indices of all six volumes in this series, going back twelve years.

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Produktdetails

• Verlag: Oxford University Press
• Seitenzahl: 280
• Erscheinungstermin: 20. Oktober 2017
• Englisch
• ISBN-13: 9780190646172
• Artikelnr.: 54561282

Autorenporträt

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.

Inhaltsangabe

* 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