Comprehensive Organic Name Reactions and Reagents
(Sprache: Englisch)
With its coverage of 701 organic name reactions and reagents, this three-volume set is the largest, most up-to-date major reference work of its kind. It offers students and professional chemists a valuable resource for conducting experiments and performing...
Leider schon ausverkauft
versandkostenfrei
Buch (Gebunden)
322.40 €
161 DeutschlandCard Punkte
sammeln
- Lastschrift, Kreditkarte, Paypal, Rechnung
- Kostenlose Rücksendung
- Ratenzahlung möglich
Produktdetails
Produktinformationen zu „Comprehensive Organic Name Reactions and Reagents “
Klappentext zu „Comprehensive Organic Name Reactions and Reagents “
With its coverage of 701 organic name reactions and reagents, this three-volume set is the largest, most up-to-date major reference work of its kind. It offers students and professional chemists a valuable resource for conducting experiments and performing a broad range of applications, from pharmaceuticals to plastics to pesticides. Each reaction listing is clearly organized into uniform sections that allow readers to quickly gather the information they need to conduct their own experimental proceduresComprehensive Organic Name Reactions and Reagents offers several features that help readers gather information quickly and conduct their experiments successfully:
* Chemical abbreviations list the abbreviation, the chemical's full name, its structure, and page references
* Schematic reaction index offers a quick overview of each reaction
* Reaction summaries provide basic information about each name reaction
* Reaction type summaries categorize and organize all related name reactions according to the type of transformation (e.g., oxidation, reduction, synthesis of alkenes, etc.)
- The most comprehensive resource available for students and bench chemists navigating the ever-growing group of named reactions and reagents
- Contains detailed reaction schemes and mechanism illustrations for each listing
- Includes information on the application of each named reaction, as well as details on experimental procedures and related reactions
- Offers biographical information on the person (or persons) for which the reaction is named
- Contains detailed reaction schemes and mechanism illustrations for each listing
- Includes information on the application of each named reaction, as well as details on experimental procedures and related reactions
- Offers biographical information on the person (or persons) for which the reaction is named
Inhaltsverzeichnis zu „Comprehensive Organic Name Reactions and Reagents “
Preface.Acknowledgments.
Autobiography.
Chemical Abbreviations.
PART ONE.
1. Abnormal Claisen Rearrangement.
2. Acetoacetic Ester Condensation.
3. Acetoacetic Ester Synthesis.
4. Acyloin Condensation.
5. Acyloin Rearrangement.
6. Adkins Catalyst.
7. Ainley and King Synthesis.
8. Akabori Amino Acid Reaction.
9. Albright-Goldman Oxidation.
10. Alder Ene Reaction.
11. Alder-Rickert Reaction.
12. Aldol Reaction and Aldol Condensation.
13. Algar-Flynn-Oyamada (AFO) Reaction.
14. Alkene Metathesis.
15. Allan-Robinson Condensation.
16. Allylic Rearrangement.
17. Amadori Rearrangement.
18. Andrussow Process.
19. Angeli-Remini Reaction.
20. ANRORC Rearrangement.
21. Anschutz Anthracene Synthesis.
22. Appel Reaction.
23. Arens-Van Dorp Reaction.
24. Arndt-Eistert Synthesis.
25. Asinger Reaction.
26. Aston-Greenburg Rearrangement.
27. Atherton-Todd Reaction.
28. Auwers-Skita Rule.
29. Aza-Claisen Rearrangement.
30. Baddeley Isomerization.
31. Baeyer Diarylmethane Synthesis.
32. Baeyer-Drewson Reaction.
33. Baeyer Indole Synthesis.
34. Baeyer Oxindole Synthesis.
35. Baeyer Pyridine Synthesis.
36. Baeyer-Villiger Oxidation.
37. Bailey Peptide Synthesis.
38. Bakelite Process.
39. Baker-Ollis Sydnones Synthesis.
40. Baker-Venkataraman Rearrangement.
41. Ball-Goodwin-Morton Oxidation.
42. Bally-Scholl Reaction.
43. Balsohn Alkylation.
44. Balz-Schiemann Reaction.
45. Bamberger Rearrangement.
46. Bamford-Stevens Reaction.
47. Barbier Reaction.
48. Barbier-Wieland Degradation.
49. Bardhan Sengupta Synthesis.
50. Bargellini Condensation.
51. Bart Reaction.
52. Bartoli Indole Synthesis.
53. Barton Decarboxylation.
54. Barton Deoxygenation.
55. Barton Reaction.
56. Barton-Kellogg Olefination.
57. Barton-Zard Pyrrole Synthesis.
58. Batcho-Leimgruber Indole Synthesis.
59. Baudisch Reaction.
60.
... mehr
Baumann-Fromm Thiophene Synthesis.
61. Baumgarten -Amino Ketone Synthesis.
62. Baylis-Hillman Reaction.
63. B'echamp Reduction.
64. Beckmann Rearrangement and Beckmann Fragmentation.
65. Bedoukian Halogenation.
66. B'ehal-Sommelet Rearrangement.
67. Beirut Reaction.
68. Bellus-Claisen Rearrangement.
69. B'enary Reaction.
70. Benkeser Reduction.
71. Benzidine Rearrangement.
72. Benzilic Acid Rearrangement.
73. Benzoin Condensation.
74. Bergius Process.
75. Bergman Cyclization.
76. Bergmann Degradation.
77. Bergmann-Stern Azlactone Synthesis.
78. Bergmann-Zervas Peptide Synthesis.
79. Bernthsen Reaction.
80. Berti Olefination.
81. Bertram-Walbaum Reaction.
82. Betti Reaction.
83. Biginelli Reaction.
84. Birch Reduction.
85. Birckenbach-Goubeau Halogenation.
86. Birnbaum-Simonini Reaction.
87. Bischler Reaction.
88. Bischler-Napieralski Isoquinoline Synthesis.
89. Black Rearrangement.
90. Blaise Ketone Synthesis.
91. Blaise Reaction.
92. Blanc Chloromethylation.
93. Blanc Rule.
94. Blomquist Cyclic Ketone Synthesis.
95. Bobbitt Reaction.
96. Bodroux Amide Synthesis.
97. Bodroux-Chichibabin Reaction.
98. B¨oeseken Oxidation.
99. Bogert-Cook Synthesis.
100. Bohn-Schmidt Reaction.
101. Boord Olefin Synthesis.
102. Borsche-Berkhout Reaction.
103. Borsche-Drechsel Reaction.
104. Borsche-Koelsch Cinnoline Synthesis.
105. Bougault Reaction.
106. Boulton-Katritzky Rearrangement.
107. Bourgel Alkyne Synthesis.
108. Bouveault Aldehyde Synthesis.
109. Bouveault-Blanc Reduction.
110. Boyland-Sims Oxidation.
111. Bradsher Cyclization.
112. Bradsher Cycloaddition.
113. Bradsher Pyridinium Salt Synthesis.
114. Brandi-Guarna Reaction.
115. Breckpot -Lactam Synthesis.
116. Bredt's Rule.
117. Brook Rearrangement.
118. Brown Hydroboration.
119. Bruckner Isoquinoline Synthesis.
120. Bucherer Carbazole Synthesis.
61. Baumgarten -Amino Ketone Synthesis.
62. Baylis-Hillman Reaction.
63. B'echamp Reduction.
64. Beckmann Rearrangement and Beckmann Fragmentation.
65. Bedoukian Halogenation.
66. B'ehal-Sommelet Rearrangement.
67. Beirut Reaction.
68. Bellus-Claisen Rearrangement.
69. B'enary Reaction.
70. Benkeser Reduction.
71. Benzidine Rearrangement.
72. Benzilic Acid Rearrangement.
73. Benzoin Condensation.
74. Bergius Process.
75. Bergman Cyclization.
76. Bergmann Degradation.
77. Bergmann-Stern Azlactone Synthesis.
78. Bergmann-Zervas Peptide Synthesis.
79. Bernthsen Reaction.
80. Berti Olefination.
81. Bertram-Walbaum Reaction.
82. Betti Reaction.
83. Biginelli Reaction.
84. Birch Reduction.
85. Birckenbach-Goubeau Halogenation.
86. Birnbaum-Simonini Reaction.
87. Bischler Reaction.
88. Bischler-Napieralski Isoquinoline Synthesis.
89. Black Rearrangement.
90. Blaise Ketone Synthesis.
91. Blaise Reaction.
92. Blanc Chloromethylation.
93. Blanc Rule.
94. Blomquist Cyclic Ketone Synthesis.
95. Bobbitt Reaction.
96. Bodroux Amide Synthesis.
97. Bodroux-Chichibabin Reaction.
98. B¨oeseken Oxidation.
99. Bogert-Cook Synthesis.
100. Bohn-Schmidt Reaction.
101. Boord Olefin Synthesis.
102. Borsche-Berkhout Reaction.
103. Borsche-Drechsel Reaction.
104. Borsche-Koelsch Cinnoline Synthesis.
105. Bougault Reaction.
106. Boulton-Katritzky Rearrangement.
107. Bourgel Alkyne Synthesis.
108. Bouveault Aldehyde Synthesis.
109. Bouveault-Blanc Reduction.
110. Boyland-Sims Oxidation.
111. Bradsher Cyclization.
112. Bradsher Cycloaddition.
113. Bradsher Pyridinium Salt Synthesis.
114. Brandi-Guarna Reaction.
115. Breckpot -Lactam Synthesis.
116. Bredt's Rule.
117. Brook Rearrangement.
118. Brown Hydroboration.
119. Bruckner Isoquinoline Synthesis.
120. Bucherer Carbazole Synthesis.
... weniger
Autoren-Porträt von Zerong Wang
Dr. Zerong Wang earned his Ph.D. at Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences. He went on to a postdoctoral at the University of California, Berkeley to study enolate chemistry followed by a second postdoctoral at York University to explore the synthesis of nucleoside analogues. Dr. Wang is currently an Associate Professor at the University of Houston-Clear Lake, with research interests in photochemistry, nucleosides, heterocycles, computational chemistry, and material science.
Bibliographische Angaben
- Autor: Zerong Wang
- 2009, 1. Auflage, Maße: 18,9 x 26,2 cm, Gebunden, Englisch
- Verlag: Wiley & Sons
- ISBN-10: 0471704504
- ISBN-13: 9780471704508
- Erscheinungsdatum: 24.07.2009
Sprache:
Englisch
Pressezitat
Kommentar zu "Comprehensive Organic Name Reactions and Reagents"
0 Gebrauchte Artikel zu „Comprehensive Organic Name Reactions and Reagents“
| Zustand | Preis | Porto | Zahlung | Verkäufer | Rating |
|---|
Schreiben Sie einen Kommentar zu "Comprehensive Organic Name Reactions and Reagents".
Kommentar verfassen