LEADER 00000cam  2200000 a 4500 
001    ocm57143283 
003    OCoLC 
005    20090109134356.0 
008    041126t20052005njua     b    001 0 eng   
010      2004028304 
020    0470010401|q(acid-free paper) 
020    9780470010402|q(acid-free paper) 
020    047001041X|q(pbk. : acid-free paper) 
020    9780470010419|q(pbk. : acid-free paper) 
035    (OCoLC)57143283 
040    DLC|beng|cDLC|dBAKER|dNBU|dNLGGC|dBTCTA|dLVB|dYDXCP|dOCLCG
       |dSTJ 
041 1  eng|hger 
049    STJR 
050 00 QD291|b.L3513 2005 
082 00 547/.2|222 
084    35.50|2bcl 
092    547.2|bL372N 
100 1  Laue, Thomas,|d1960- 
240 10 Namen- und Schlagwort-Reaktionen der organischen Chemie.
       |lEnglish 
245 10 Named organic reactions /|cThomas Laue and Andreas Plagens
       ; translated into English by Claus Vogel. 
250    Second edition. 
264  1 Hoboken, NJ :|bWiley,|c[2005] 
264  4 |c©2005 
300    x, 310 pages :|billustrations ;|c24 cm 
336    text|btxt|2rdacontent 
337    unmediated|bn|2rdamedia 
338    volume|bnc|2rdacarrier 
504    Includes bibliographical references and index. 
505 0  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. 
650  0 Chemical reactions. 
650  0 Chemistry, Organic. 
700 1  Plagens, Andreas,|d1965- 
856 41 |3Table of contents only|uhttp://www.loc.gov/catdir/toc/
       ecip054/2004028304.html 
856 42 |3Publisher description|uhttp://www.loc.gov/catdir/
       enhancements/fy0617/2004028304-d.html 
938    YBP Library Services|bYANK|n2168661 
938    Baker & Taylor|bBKTY|c140.00|d.00|i0470010401|n0006170994
       |sactive 
938    Baker & Taylor|bBKTY|c65.00|d.00|i047001041X|n0006170995
       |sactive 
994    01|bSTJ