Organic synthesis : state of the art 2009-2011 / Douglass F. Taber.

Format:

Book

Author/Creator:

Taber, D. F. (Douglass F.), 1948-

Series:

Oxford scholarship online.

Oxford scholarship online

Language:

English

Subjects (All):

Organic compounds--Synthesis--Research.

Organic compounds.

Carbon compounds--Research.

Carbon compounds.

Physical Description:

1 online resource (xi, 250 pages ) illustrations (black and white)

Edition:

1st ed.

Place of Publication:

Oxford : Oxford University Press, 2013.

Language Note:

English

Summary:

This go-to reference focuses on the most important recent developments in organic synthesis, and includes a succinct analysis of the significance and applicability of each new synthetic method.

Contents:

Cover

Contents

Preface

Organic Functional Group Interconversion and Protection

1. Best Synthetic Methods: Functional Group Transformations

2. Functional Group Transformation: The Castle Synthesis of Celogentin C

3. Organic Functional Group Conversion

4. Advances in Organic Functional Group Transformation

5. Organic Functional Group Transformation

6. Best Synthetic Methods: Reduction

7. Best Synthetic Methods: Oxidation

8. Best Synthetic Methods: Oxidation and Reduction

9. Oxidation and Reduction

10. Organic Functional Group Protection

11. Functional Group Protection: The Kraus Synthesis of Bauhinoxepin J

12. Functional Group Protection

13. Organic Functional Group Protection

14. Organic Functional Group Protection and Deprotection

Flow Methods

15. Flow Methods for Organic Synthesis

C-H Functionalization

16. C-H Functionalization: The White Synthesis of 6-Deoxyerythronolide B

17. C-H Functionalization: The Chen Synthesis of Celogentin C

18. Functionalization and Homologation of C-H Bonds

Carbon-Carbon Bond Construction

19. New Methods for Carbon-Carbon Bond Construction

20. Best Synthetic Methods: C-C Bond Construction

21. New Methods for C-C Bond Construction

22. New Methods for C-C Bond Construction: The Burke Synthesis of (-)-Peridinin

23. Carbon-Carbon Bond Formation

Reactions of Alkenes

24. Best Synthetic Methods: Reactions of Alkenes

25. Alkene Reactions: The Dabdoub/Baroni Synthesis of ( ± )-Dihydroactinidiolide

26. Reactions of Alkenes

27. Functionalization and Homologation of Alkenes

Alkene and Alkyne Metathesis

28. Advances in Alkene Metathesis: The Hoveyda Synthesis of (+)-Quebrachamine.

29. Alkene and Alkyne Metathesis: Navenone B (Cossy), (+)-Asperpentyn (Daesung Lee), (-)-Amphidinolide K (Eun Lee), Norhalichondrin B (Phillips)

30. Progress in Alkene and Alkyne Metathesis: (+)-5-epi-Citreoviral (Funk) and ( ± )-Poitediol (Vanderwal)

31. Alkene and Alkyne Metathesis: Grandisol (Goess), 8-Epihalosilane (Kouklovsky/Vincent), (+)-Chinensiolide B (Hall)

32. Alkene and Alkyne Metathesis: (+)-Anamarine (Sabitha), (±)-Pseudotabersonine (Martin), Lactimidomycin (Fürstner)

Enantioselective Construction of Acyclic Stereogenic Centers

33. Enantioselective Preparation of Alcohols and Amines: The Suh Synthesis of (-)-Macrosphelide J

34. Enantioselective Preparation of Alcohols and Amines

35. Construction of Oxygenated and Aminated Stereogenic Centers

36. Enantioselective Preparation of Alcohols and Amines: The Lam Synthesis of (+)-Tanikolide

37. Enantioselective Construction of Alkylated Centers: The Maier Synthesis of Platencin

38. Enantioselective Construction of Alkylated Stereogenic Centers

39. Construction of Alkylated Stereogenic Centers

40. Enantioselective Preparation of Alkylated Stereogenic Centers

41. Construction of Arrays of Stereogenic Centers: The Zhang Synthesis of (+)-Podophyllotoxin

42. Enantioselective Construction of Arrays of Stereogenic Centers: The Breit Synthesis of (+)-Bourgeanic Acid

43. Stereocontrolled Construction of Arrays of Stereogenic Centers: The Mullins Synthesis of (-)-Lasiol

44. Establishing Arrays of Stereogenic Centers: The Sato/Chida Synthesis of (-)-Kainic Acid

Construction of C-O Rings

45. Stereoselective C-O Ring Construction: The Jamison Synthesis of (-)-Gloeosporone

46. Stereocontrolled Construction of C-O Rings: The Seeberger/Hilvert Synthesis of KDN

47. C-O Ring Construction: The Theodorakis Synthesis of (-)-Englerin A.

48. Synthesis of Naturally Occurring Cyclic Ethers: Boivivianin B (Murakami), SC-&amp

#916

[sup(13)]-9-IsoF (Taber), Brevisamide (Panek, Lindsley, Ghosh), Gambierol (Mori)

49. Stereoselective C-O Ring Construction: (+)-Pachastrissamine (Fujii/Ohno), Aspalathin (Minehan), (+)-Varitriol (Ghosh), Aspercyclide A (Spivey), Etnangien (Menche)

50. C-O Ring Construction: (-)-Sclerophytin A (Morken), (+)-Dictyosphaeric Acid (Taylor), Goniothalesdiol A (Xie/She), (-)-7-Deoxyloganin (Lupton), (-)-Apicularen A (Uenishi), L-783, 277 (Banwell)

Construction of C-N Rings

51. Stereocontrolled C-N Ring Construction: The Takayama Synthesis of Lycoposerramine-C

52. Stereocontrolled C-N Ring Construction: The Pyne Synthesis of Hyacinthacine B[sub(3)]

53. C-N Ring Construction: The Zakarian Synthesis of (-)-Rhazinilam

54. C-N Ring Construction: The Synthesis of Decursivine by Mascal and by Jia

55. Alkaloid Synthesis: (S)-Nicotine (Helmchen), (+)-CP-99,994 (Shi), (-)-Adaline (Yu), (-)-Securinine (Bayón/Figueredo), Alkaloid 223A (Aubé), (-)-Huperzine A (Fukuyama)

56. Synthesis of C-N Natural Products: (-)-&amp

#945

-Kainic Acid (Helmchen), (+)-Tylophorine (Opatz), (-)-Lycoperine A (Rychnovsky), Fluvirucidine A[sub(2)] (Suh), Complanidine A (Sarpong)

57. Alkaloid Synthesis: (+)-Preussin (Britton), (±)-Xenovenine (Livinghouse), (+)-Subincanadine F (Li), (±)-Strychnine (Reissig), (-)-Virginiamycin M[sub(2)] (Panek)

58. Alkaloid Synthesis: Mearsine (Taylor), Cephalotaxine (Li), Cocaine (Shing), Quinine (Hatakeyama), Cleavamine (Bennasar), Strychnine (Vanderwal)

Substituted Benzene Derivatives

59. Benzene Derivatives: The Tanino-Miyashita Synthesis of Zoanthenol

60. Substituted Benzenes: The Saikawa/Nakata Synthesis of Kendomycin

61. Substituted Benzenes: The Kirsch Synthesis of Cybrodol.

62. Substituted Benzenes: The Piers/Lau Synthesis of Hamigeran B

Heteroaromatic Derivatives

63. Heteroaromatic Construction: The Jia Synthesis of (-)-cis-Clavicipitic Acid

64. Heteroaromatics: The Mal Synthesis of Clausevatine D

65. Heteroaromatic Construction: The Fukuyama Synthesis of Tryprostatin A

66. Heteroaromatic Construction: The Wipf Synthesis of Cycloclavine

Organocatalyzed C-C Ring Construction

67. Organocatalytic Carbocyclic Construction: The Christmann Synthesis of (+)-Rotundial

68. Enantioselective Organocatalytic C-C Ring Construction

69. Organocatalysis of Carbocyclic Construction: The MacMillan Synthesis of (+)-Frondosin B

70. Organocatalyzed C-C Ring Construction: The Thomson Synthesis of Streptorubin B

Transition Metal Catalyzed C-C Ring Construction

71. Metal-Mediated Carbocyclic Construction: The Kobayashi Synthesis of (+)-Fomitellic Acid B

72. Transition-Metal Catalyzed Ring Construction: The Yu Synthesis of &amp

-Agorafuran

73. Metal-Mediated Carbocyclic Construction: The Simpkins Synthesis of Ialibinones A and B

74. Metal Mediated C-C Ring Construction: The Nevado Route to (-)-Frondosin A

Intermolecular and Intramolecular Diels-Alder Reactions

75. Tethered Diels-Alder Cycloaddition: (±)-Neovibsanin B (Imagawa, Nishizawa), Valerenic Acid (Mulzer), (-)-Himandrine (Movassaghi), (±)-Pallavicinolide A (Wong), (+)-Phomopsidin (Nakada)

76. Intramolecular Diels-Alder Cycloaddition: Brombyin II (Lygo), Ptilocaulin (Livinghouse), Bistellettadine A (Snider), (-)-Pycnanthuquinone C (Trauner), (+)-Caribenol A (Li/Yang)

Stereocontrolled C-C Ring Construction

77. Carbocyclic Construction: The Deng Synthesis of (-)-Plicatic Acid

78. New Methods for Carbocyclic Construction: The Kim Synthesis of Pentalenene.

79. Other Methods for Carbocyclic Construction: The Porco Synthesis of (-)-Hyperibone K

80. Stereoselective Carbocyclic Construction: The Metz Synthesis of (±)-Codeine

Classics in Total Synthesis

81. The Williams Synthesis of (-)-4-Hydroxydictyolactone

82. The Nakada Synthesis of (-)-FR182877

83. The Trost Synthesis of (-)-Pseudolaric Acid B

84. The Corey Synthesis of (+)-Lupeol

85. The Dixon Synthesis of (-)-Nakadomarin A

86. The Magnus Synthesis of (±)-Codeine

87. The Nicolaou Synthesis of (+)-Hirsutellone B

88. The Nicolaou Synthesis of (+)-Vannusal

89. The Baran Synthesis of Vinigrol

90. The Overman Synthesis of Briarellin F

91. The Shair Synthesis of Cephalostatin 1

92. The Chen Synthesis of (-)-Nakiterpiosin

93. The Tanino Synthesis of (-)-Glycinoeclepin A

94. The Boger Synthesis of (-)-Vindoline

95. The Bradshaw/Bonjoch Synthesis of (-)-Anominine

96. The Ma Synthesis of (-)-GB 13

97. The Trost Synthesis of Bryostatin 16

98. The Li/Yang Synthesis of (±)-Maoecrystal V

99. The Funk Synthesis of (-)-Nakadomarin A

100. The Boger Synthesis of (+)-Complestatin

101. The Overman Synthesis of (-)-Actinophyllic Acid

102. The Tanino/Miyashita Synthesis of Solanoeclepin A

103. The Rawal Synthesis of N-Methylwelwitindolinone D Isonitrile

104. The Garg Synthesis of (±)-Aspidophylline A

Author Index

A

B

C

D

E

F

G

H

I

J

K

L

M

N

O

P

Q

R

S

T

U

V

W

X

Y

Z

Reaction Index

W.

Notes:

Includes index.

Description based on metadata supplied by the publisher and other sources.

ISBN:

0-19-756332-5

0-19-996573-0

OCLC:

848902288