Record Display for the EPA National Library Catalog

RECORD NUMBER: 413 OF 670

Main Title Named organic reactions
Author Laue, Thomas
Other Authors
Author Title of a Work
Plagens, Andreas
Publisher Wiley,
Year Published 2005
OCLC Number 57143283
ISBN 0470010401 (acid-free paper) 047001041X (pbk. : acid-free paper)
Subjects Chemical reactions ; Chemistry, Organic
Internet Access
Description Access URL
http://www.loc.gov/catdir/enhancements/fy0617/2004028304-d.html
Holdings
Library Call Number Additional Info Location Last
Modified
Checkout
Status
EKBM  QD291.L3513 2005 Research Triangle Park Library/RTP, NC 04/28/2006
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.