OXFORD UNIVERSITY PRESS

Organic Synthesis: State of the Art 2011-2013

ISBN : 9780190200794

参考価格(税込): 
¥20,020
著者: 
Douglass F. Taber; Tristan Lambert
ページ
280 ページ
フォーマット
Hardcover
サイズ
162 x 238 mm
刊行日
2015年01月
メール送信
印刷

Organic Synthesis: State of the Art 2011-2013 is a convenient, concise reference that summarizes the most important current developments in organic synthesis, from functional group transformations to complex natural product synthesis. The fifth volume in the esteemed State of the Art series, the book compiles two years' worth of Douglass Taber's popular weekly column Organic Chemistry Highlights. The series is an invaluable resource, leading chemists quickly and easily to the most significant developments in the field. The book is logically divided into two sections: the first section focuses on specific topics in organic synthesis, such as C-N Ring Construction and Carbon-Carbon Bond Formation. Each topic is presented using the most significant publications within those areas of research. The journal references are included in the text. The second section focuses on benchmark total syntheses, with an analysis of the strategy for each, and discussions of pivotal transformations. Synthetic organic chemistry is a complex and rapidly growing field, with additional new journals appearing almost every year. Staying abreast of recent research is a daunting undertaking. This book is an ideal tool for both practicing chemists and students, offering a rich source of information and suggesting fruitful pathways for future investigation.

目次: 

Contents
Preface
Organic Functional Group Interconversion and Protection
1. Functional Group Transformations May 14, 2012
2. Functional Group Interconversion October 22, 2012
3. Functional Group Interconversion May 13, 2013
4. Functional Group Interconversion October 28, 2013
5. Reduction and Oxidation May 21, 2012
6. Functional Group Oxidation and Reduction November 12, 2012
7. Functional Group Oxidation May 20, 2013
8. Functional Group Reduction May 27, 2013
9. Functional Group Protection May 28, 2012
10. Functional Group Protection October 29, 2012
11. Functional Group Protection June 12, 2013
12. Functional Group Protection November 11, 2013
Flow Methods
13. Develop of Flow Reactions September 24, 2012
14. Flow Chemistry March 25, 2013
15. Flow Chemistry September 30, 2013
C-H Functionalization
16. C-H Functionalization: The Ono/Kato/Dairi Synthesis of Fusiocca-1,10(14)-diene-3,8?,16-triol March 19, 2012
17. C-H Functionalization September 17, 2012
18. C-H Functionalization: The Hatakeyama Synthesis of (-)-Kaitocephalin January 28, 2013
19. C-H Functionalization September 16, 2013
20. Natural Product Synthesis by C-H Functionalization: (+-)-Allokainic Acid (Wee), (-)-Cameroonan-7?-ol (Taber), (+)-Lithospermic Acid (Yu), (-)-Manabacanine (Kroutil), Streptorubin B and Metacycloprodigiosin (Challis) January 30, 2012
21. Natural Product Synthesis by C-H Functionalization: (-)-Zampanolide (Ghosh), Muraymycin D2 (Ichikawa), (+)-Sundiversifolide (Iwabuchi), (+)-Przewalskin B (Zhang/Tu), Artemisinin (Wu) June 11, 2012
Carbon-Carbon Bond Construction
22. Carbon-Carbon Bond Formation: The Bergman Synthesis of (+)-Fuligocandin B March 12, 2012
23. C-C Bond Formation: The Petrov Synthesis of Combretastatin A-4 June 18, 2012
24. Carbon-Carbon Bond Construction: The Baran Synthesis of (+)-Chromazonarol March 11, 2013
25. Carbon-Carbon Bond Construction July 29, 2013
26. Reactions Involving C-C Bond Cleavage September 23, 2013
Reactions of Alkenes
27. Reactions of Alkenes: The RajanBabu Synthesis of Pseudopterosin G-J Aglycone Dimethyl Ether March 26, 2012
28. Reactions of Alkenes September 10, 2012
29. Reactions of Alkenes March 18, 2013
30. Synthesis and Reactions of Alkenes September 9, 2013
31. Advances in Alkene Metathesis: The Kobayashi Synthesis of (+)-TMC-151C January 23, 2012
Enantioselective Construction of Acyclic Stereogenic Centers
32. Enantioselective Synthesis of Alcohols and Amines: The Ichikawa Synthesis of (+)-Geranyllinaloisocyanide February 13, 2012
33. Enantioselective Synthesis of Alcohols and Amines: The Fujii/Ohno Synthesis of (+)-Lysergic Acid July 16, 2012
34. Asymmetric C-Heteroatom Bond Formation February 11, 2013
35. Construction of Single Stereocenters July 15, 2013
36. Enantioselective Construction of Alkylated Centers: The Shishido Synthesis of (+)-Helianane February 20, 2012
37. Enantioselective Synthesis of Alkylated Centers: The Fukuyama Synthesis of (-)-Histrionicotoxin July 23, 2012
38. Asymmetric C-C Bond Formation February 18, 2013
39. Arrays of Stereogenic Centers: The Davies Synthesis of Acosamine February 27, 2012
40. Construction of Alkylated Stereocenters: The Deng Synthesis of (-)-Isoacanthodoral July 8, 2013
41. Arrays of Stereogenic Centers: The Barker Synthesis of (+)-Galbelgin July 30, 2012
42. Arrays of Stereogenic Centers: The Carbery Synthesis of Mycestericin G February 25, 2013
43. Construction of Stereochemical Arrays July 22, 2013
Construction of C-O Rings
44. Stereoselective C-O Ring Construction: The Keck Synthesis of Bryostatin 1 January 9, 2012
45. C-O Ring Construction: The Georg Synthesis of Oximidine II April 9, 2012
46. C-O Ring Construction: The Reisman Synthesis of (-)-Acetylaranotin January 14, 2013
47. C-O Ring Formation April 8, 2013
48. C-O Ring Construction: (+)-Varitriol (Liu), (+)-Isatisine A (Panek), (+)-Herboxidiene / GEX1A (Ghosh), (-)-Englerin A (Chain), Platensimycin (Lear/Wright) January 16, 2012
49. C-O Natural Products: (-)-Hybridalactone (Furstner), (+)- Anthecotulide (Hodgson), (-)-Kumausallene (Tang), (+-)-Communiol E (Kobayashi), (-)-Exiguolide (Scheidt), Cyanolide A (Rychnovsky) April 16, 2012
50. C-O Ring Containing Natural Products January 21, 2013
51. Total Synthesis of C-O Ring-Containing Natural Products April 15, 2013
Construction of C-N Rings
52. C-N Ring Construction: The Harrity Synthesis of Quinolizidine (-)-217A April 23, 2012
53. New Methods for C-N Ring Construction November 19, 2012
54. C-N Ring Construction: The Fujii/Ohno Synthesis of (-)-Quinocarcin April 22, 2013
55. C-N Ring Construction: The Hoye Synthesis of (+-)-Leuconolactam November 18, 2013
56. Alkaloid Synthesis: (-)-?-Kainic Acid (Cohen), Hyacinthacine A2 (Fox), (-)-Agelastatin A (Hamada), (+)-Luciduline (Barbe), (+)-Lunarine (Fan), (-)-Runanine (Herzon) April 30, 2012
57. Alkaloid Synthesis: Indolizidine 207A (Shenvi), (-)-Acetylaranotin (Reisman), Flinderole A (May), Isohaouamine B (Trauner), (-)-Strychnine (MacMillan) November 26, 2012
58. Alkaloid Synthesis: (+)-Deoxoprosopinine (Krishna), Alkaloid (-)-205B (Micalizio), FR901483 (Huang), (+)-Ibophyllidine (Kwon), (-)-Lycoposerramine-S (Fukuyama), (+-)-Crinine (Lautens) April 29, 2013
59. Alkaloid Synthesis: Lycoposerramine Z (Bonjoch), Esermethole (Shishido), Goniomitine (Zhu), Grandisine (Taylor), Reserpine (Jacobsen) November 25, 2013
Substituted Benzene Derivatives
60. Substituted Benzenes: The Reddy Synthesis of Isofregenedadiol June 25, 2012
61. Substituted Benzenes: The Alvarez-Manzaneda Synthesis of (-)-Akaol A October 8, 2012
62. Substituted Benzenes: The Subba Reddy Synthesis of 7-Desmethoxyfusarentin June 17, 2013
63. Substituted Benzenes: The Gu Synthesis of Rhazinal October 14, 2013
Heteroaromatic Derivatives
64. Heteroaromatic Construction: The Sperry Synthesis of (+)-Terreusinone July 9, 2012
65. Heteroaromatic Construction: The Sato Synthesis of (-)-Herbindole October 15, 2012
66. Advances in Heterocyclic Aromatic Construction June 24, 2013
67. Synthesis of Heteroaromatics October 21, 2013
Organocatalyzed C-C Ring Construction
68. Organocatalytic Carbocyclic Construction: The You Synthesis of (-)-Mesembrine August 20, 2012
69. Organocatalyzed Carbocyclic Construction: (+)-Roseophilin (Flynn) and (+)-Galbulin (Hong) December 10, 2012
70. Organocatalytic C-C Ring Construction: Prostaglandin F2? (Aggarwal) August 12, 2013
71. Organocatalyzed C-C Ring Construction: The Hayashi Synthesis of PGE1 Me Ester December 16, 2013
Metal-Mediated C-C Ring Construction
72. Metal-Mediated Carbocyclic Construction: The Chen Synthesis of Ageliferin August 13, 2012
73. Metal-Mediated Carbocyclic Construction: The Whitby Synthesis of (+)-Mucosin December 17, 2012
74. Metal-Mediated C-C Ring Construction: (+)-Shiromool (Baran) August 19, 2013
75. Metal-Mediated Ring Construction: The Hoveyda Synthesis of (-)-Nakadomarin A December 9, 2013
Intermolecular and Intramolecular Diels-Alder Reactions
76. Intramolecular Diels-Alder Cycloaddition: 7-Isocyanoamphilecta-11(20),15-diene (Miyaoka), (-)-Scabronine G (Kanoh), Basiliolide B (Stoltz), Hirsutellone B (Uchiro), Echinopine A (Chen) August 27, 2012
77. Diels-Alder Cycloaddition: Fawcettimine (Williams), Apiosporic Acid (Helmchen), Marginatone (Abad-Somovilla), Okilactomycin (Hoye), Vinigrol (Barriault), Plakotenin (Bihlmeier/Klopper) December 24, 2012
78. Diels-Alder Cycloaddition: Defucogilvocarcin V (Bodwell), (+)-Carrisone (Danishefsky), (+)-Fusarisetin A (Theodorakis), 9?-Presilphiperfolan-1?-ol (Stoltz), 7-Isocyano-11(20), 14-epiamphilectadiene (Shenvi) August 26, 2013
79. Diels-Alder Cycloaddition: (+)-Armillarivin (Banwell), Gelsemiol (Gademann), (+)-Frullanolide (Liao), Myceliothermophin A (Uchiro), Peribysin E (Reddy), Caribenol A (Li/Yang) December 23, 2013
Stereocontrolled C-C Ring Construction
80. Chloranthalactone (Liu), Rumphellaone A (Kuwahara), Lactiflorin (Bach), Echinosporin (Hale), Harveynone (Taylor), (6,7-deoxy)-Yuanhuapin (Wender) December 31, 2012
81. Other Methods for C-C Ring Construction: The Liang Synthesis of Echinopine B December 30, 2013
Classics in Total Synthesis
82. The Reisman Synthesis of (+)-Salvileucalin B January 2, 2012
83. The Theodorakis Synthesis of (-)-Jiadifenolide February 6, 2012
84. The Yamashita/Hirama Synthesis of Cortistatin A March 5, 2012
85. The Reisman Synthesis of (-)-Maoecrystal Z April 2, 2012
86. The Tan/Chen/Yang Synthesis of Schindilactone A May 7, 2012
87. The Garg Synthesis of (-)-N-Methylwelwitindolinone C June 4, 2012
88. The Krische Synthesis of Bryostatin 7 July 2, 2012
89. The Fukuyama Synthesis of Gelsemoxonine August 6, 2012
90. The Carreira Synthesis of (+)-Daphmanidin E September 3, 2012
91. The Qin Synthesis of (+)-Gelsemine October 1, 2012
92. The Carreira Synthesis of Indoxamycin B November 5, 2012
93. The Nicolaou/Li Synthesis of Tubingensin A December 3, 2012
94. The Thomson Synthesis of (-)-GB17 January 7, 2013
95. The Li Synthesis of (-)-Fusarisetin A February 4, 2013
96. The Carreira Synthesis of (-)-Dendrobine March 4, 2013
97. The Vanderwal Synthesis of Echinopine B April 1, 2013
98. The Dixon Synthesis of Manzamine A May 6, 2013
99. The Williams Synthesis of (-)-Khayasin June 3, 2013
100. The Kuwahara Synthesis of Paspalinine July 1, 2013
101. The Ma Synthesis of Gracilamine August 5, 2013
102. The Carreira Synthesis of (+-)-Gelsemoxonine September 2, 2013
103. The Evans Synthesis of (-)-Nakadomarin A October 7, 2013
104. The Procter Synthesis of (+)-Pleuromutilin November 4, 2013
105. The Harran Synthesis of (+)-Roseophilin December 2, 2013

著者について: 

Douglass F. Taber, who currently lives in Philadelphia, is Professor Emeritus at the University of Delaware. Professor Taber published more than 200 articles in the field of organic chemistry, and authored eight chapters and several books. His research interests include the stereoselective synthesis of natural products, new methods in synthetic organic chemistry, and computational organometallic chemistry in organic synthesis.; Tristan Lambert is a Professor of Chemistry at Columbia University, where he heads a lab with the goal of advancing the field of organic synthesis by inventing transformative new reaction tools that will increase the speed, efficiency, and selectivity with which complex molecules may be constructed.

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