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HAWAII STATE PUBLIC LIBRARY SYSTEM
Item Information
Summary
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Laue, Thomas, 1960-
Subjects
Chemical reactions.
Chemistry, Organic.
Browse Catalog
by author:
Laue, Thomas, 1960-
by title:
Named organic reacti...
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Named organic reactions [electronic resource] / Thomas Laue and Andreas Plagens ; translated into English by Claus Vogel.
by
Laue, Thomas, 1960-
Hoboken, NJ : Wiley, c2005.
Subjects
Chemical reactions.
Chemistry, Organic.
Electronic Resource
http://hawaii.lib.overdrive.com/ContentDetails.htm?ID=FB143792-3A5F-46FF-ACC0-5FCB33F03F67
This title is available online; click here to access
ISBN:
0470026448 (electronic bk. : Adobe Reader)
Description:
x, 310 p. : ill. ; 24 cm.
Edition:
2nd ed.
Contents:
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 -- Delépine Reaction -- Diazo Coupling -- Diazotization -- Diels-Alder Reaction -- Di-[pi]-Methane Rearrangement -- Dötz Reaction -- Elbs Reaction -- Ene Reaction -- Ester Pyrolysis -- Favorskii Rearrangement -- Finkelstein Reaction -- Fischer Indole Synthesis -- Friedel-Crafts Acylation -- Friedel-Crafts Alkylation -- Friedländer 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-Büchi Reaction -- Pauson-Khand Reaction -- Perkin Reaction -- Peterson Olefination -- Pinacol Rearrangement -- Prilezhaev Reaction -- Prins Reaction -- Ramberg-Bäcklund 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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