Main Title |
Named organic reactions |
Author |
Laue, Thomas
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Other Authors |
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Publisher |
Wiley, |
Year Published |
2005 |
OCLC Number |
57143283 |
ISBN |
0470010401 (acid-free paper) 047001041X (pbk. : acid-free paper) |
Subjects |
Chemical reactions ;
Chemistry, Organic
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Internet Access |
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Holdings |
Library |
Call Number |
Additional Info |
Location |
Last Modified |
Checkout Status |
EKBM |
QD291.L3513 2005 |
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Research Triangle Park Library/RTP, NC |
04/28/2006 |
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Edition |
2nd ed. |
Collation |
x, 310 p. : ill. ; 24 cm. |
Notes |
Includes bibliographical references and index. |
Contents Notes |
Acyloin Ester Condensation -- Aldol Reaction -- Alkene Metathesis -- Arbuzov Reaction -- Arndt-Eistert Synthesis -- Baeyer-Villiger Oxidation -- Bamford-Stevens Reaction -- Barton Reaction -- Baylis-Hillman Reaction -- Beckmann Rearrangement -- Benzidine Rearrangement -- Benzilic Acid Rearrangement -- Benzoin Condensation -- Bergman Cyclization -- Birch Reduction -- Blanc Reaction -- Bucherer Reaction -- Cannizzaro Reaction -- Chugaev Reaction -- Claisen Ester Condensation -- Claisen Rearrangement -- Clemmensen Reduction -- Cope Elimination Reaction -- Cope Rearrangement -- Corey-Winter Fragmentation -- Curtius Reaction -- 1,3-Dipolar Cycloaddition -- {2+2 } Cycloaddition -- Darzens Glycidic Ester Condensation -- Delepine Reaction -- Diazo Coupling -- Diazotization -- Diels-Alder Reaction -- Di-{pi}-Methane Rearrangement -- D otz Reaction -- Elbs Reaction -- Ene Reaction -- Ester Pyrolysis -- Favorskii Rearrangement -- Finkelstein Reaction -- Fischer Indole Synthesis -- Friedel-Crafts Acylation -- Friedel-Crafts Alkylation -- Friedl ander Quinoline Synthesis -- Fries Rearrangement -- Gabriel Synthesis -- Gattermann Synthesis -- Glaser Coupling Reaction -- Glycol Cleavage -- Gomberg-Bachmann Reaction -- Grignard Reaction -- Haloform Reaction -- Hantzsch Pyridine Synthesis -- Heck Reaction -- Hell-Volhard-Zelinskii Reaction -- Hofmann Elimination Reaction -- Hofmann Rearrangement -- Hunsdiecker Reaction -- Hydroboration -- Japp-Klingemann Reaction -- Knoevenagel Reaction -- Knorr Pyrrole Synthesis -- Kolbe Electrolytic Synthesis -- Kolbe Synthesis of Nitriles -- Kolbe-Schmitt Reaction -- Leuckart-Wallach Reaction -- Lossen Reaction -- Malonic Ester Synthesis -- Mannich Reaction -- McMurry Reaction -- Meerwein-Ponndorf-Verley Reduction -- Michael Reaction -- Mitsunobu Reaction -- Nazarov Cyclization -- Neber Rearrangement -- Nef Reaction -- Norrish Type I Reaction -- Norrish Type II Reaction -- Ozonolysis -- Paterno-B uchi Reaction -- Pauson-Khand Reaction -- Perkin
Reaction -- Peterson Olefination -- Pinacol Rearrangement -- Prilezhaev Reaction -- Prins Reaction -- Ramberg-B acklund Reaction -- Reformatsky Reaction -- Reimer-Tiemann Reaction -- Robinson Annulation -- Rosenmund Reduction -- Sakurai Reaction -- Sandmeyer Reaction -- Schiemann Reaction -- Schmidt Reaction -- Sharpless Epoxidation -- Simmons-Smith Reaction -- Skraup Quinoline Synthesis -- Stevens Rearrangement -- Stille Coupling Reaction -- Stork Enamine Reaction -- Strecker Synthesis -- Suzuki Reaction -- Swern Oxidation -- Tiffeneau-Demjanov Reaction -- Vilsmeier Reaction -- Vinylcyclopropane Rearrangement -- Wagner-Meerwein Rearrangement -- Weiss Reaction -- Willgerodt Reaction -- Williamson Ether Synthesis -- Wittig Reaction -- Wittig Rearrangement -- Wohl-Ziegler Bromination -- Wolff Rearrangement -- Wolff-Kishner Reduction -- Wurtz Reaction.
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