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9780471704508

Comprehensive Organic Name Reactions and Reagents, 3 Volume Set

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  • ISBN13:

    9780471704508

  • ISBN10:

    0471704504

  • Edition: 1st
  • Format: Hardcover
  • Copyright: 2009-06-29
  • Publisher: Wiley-Interscience

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Summary

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.)

Author Biography

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.

Table of Contents

Preface
Acknowledgments
Autobiography
Chemical Abbreviations
Abnormal Claisen Rearrangement
Acetoacetic Ester Condensation
Acetoacetic Ester Synthesis
Acyloin Condensation
Acyloin Rearrangement
Adkins Catalyst
Ainley and King Synthesis
Akabori Amino Acid Reaction
Albright-Goldman Oxidation
Alder Ene Reaction
Alder-Rickert Reaction
Aldol Reaction and Aldol Condensation
Algar-Flynn-Oyamada (AFO) Reaction
Alkene Metathesis
Allan-Robinson Condensation
Allylic Rearrangement
Amadori Rearrangement
Andrussow Process
Angeli-Remini Reaction
ANRORC Rearrangement
Anschutz Anthracene Synthesis
Appel Reaction
Arens-Van Dorp Reaction
Arndt-Eistert Synthesis
Asinger Reaction
Aston-Greenburg Rearrangement
Atherton-Todd Reaction
Auwers-Skita Rule
Aza-Claisen Rearrangement
Baddeley Isomerization
Baeyer Diarylmethane Synthesis
Baeyer-Drewson Reaction
Baeyer Indole Synthesis
Baeyer Oxindole Synthesis
Baeyer Pyridine Synthesis
Baeyer-Villiger Oxidation
Bailey Peptide Synthesis
Bakelite Process
Baker-Ollis Sydnones Synthesis
Baker-Venkataraman Rearrangement
Ball-Goodwin-Morton Oxidation
Bally-Scholl Reaction
Balsohn Alkylation
Balz-Schiemann Reaction
Bamberger Rearrangement
Bamford-Stevens Reaction
Barbier Reaction
Barbier-Wieland Degradation
Bardhan Sengupta Synthesis
Bargellini Condensation
Bart Reaction
Bartoli Indole Synthesis
Barton Decarboxylation
Barton Deoxygenation
Barton Reaction
Barton-Kellogg Olefination
Barton-Zard Pyrrole Synthesis
Batcho-Leimgruber Indole Synthesis
Baudisch Reaction
Baumann-Fromm Thiophene Synthesis
Baumgarten ?-Amino Ketone Synthesis
Baylis-Hillman Reaction
B´echamp Reduction
Beckmann Rearrangement and Beckmann Fragmentation
Bedoukian Halogenation
B´ehal-Sommelet Rearrangement
Beirut Reaction
Bellus-Claisen Rearrangement
B´enary Reaction
Benkeser Reduction
Benzidine Rearrangement
Benzilic Acid Rearrangement
Benzoin Condensation
Bergius Process
Bergman Cyclization
Bergmann Degradation
Bergmann-Stern Azlactone Synthesis
Bergmann-Zervas Peptide Synthesis
Bernthsen Reaction
Berti Olefination
Bertram-Walbaum Reaction
Betti Reaction
Biginelli Reaction
Birch Reduction
Birckenbach-Goubeau Halogenation
Birnbaum-Simonini Reaction
Bischler Reaction
Bischler-Napieralski Isoquinoline Synthesis
Black Rearrangement
Blaise Ketone Synthesis
Blaise Reaction
Blanc Chloromethylation
Blanc Rule
Blomquist Cyclic Ketone Synthesis
Bobbitt Reaction
Bodroux Amide Synthesis
Bodroux-Chichibabin Reaction
B¿oeseken Oxidation
Bogert-Cook Synthesis
Bohn-Schmidt Reaction
Boord Olefin Synthesis
Borsche-Berkhout Reaction
Borsche-Drechsel Reaction
Borsche-Koelsch Cinnoline Synthesis
Bougault Reaction
Boulton-Katritzky Rearrangement
Bourgel Alkyne Synthesis
Bouveault Aldehyde Synthesis
Bouveault-Blanc Reduction
Boyland-Sims Oxidation
Bradsher Cyclization
Bradsher Cycloaddition
Bradsher Pyridinium Salt Synthesis
Brandi-Guarna Reaction
Breckpot ?-Lactam Synthesis
Bredt's Rule
Brook Rearrangement
Brown Hydroboration
Bruckner Isoquinoline Synthesis
Bucherer Carbazole Synthesis
Bucherer Reaction
Bucherer-Bergs Hydantoin Synthesis
B¿uchner Ring Expansion
B¿uchner-Curtius-Schlotterbeck Reaction
Buchwald Indoline Synthesis
Buchwald-Hartwig Amination
Burton Trifluoromethylation
Cadogan-Sundberg Indole Synthesis
Caglioti Reaction
Cahours-Hofmann Reaction
Camps Reaction
Cannizzaro Reaction
Carboni-Lindsey Reaction
Carroll Rearrangement
Castro Indole Synthesis
Castro-Stephens Coupling
Chan Rearrangement
Chapman Rearrangement
Chichibabin Amination
Chichibabin Pyridine Synthesis
Chretien-Longi Reaction
Chugaev Reaction
Ciamician-Dennstedt Reaction
Claisen Rearrangement
Claisen-Schmidt Condensation
Clauson-Kaas Reaction
Clay-Kinnear-Perren Condensation
Clayton-Jensen Chlorophosphonation
Clemmensen Reduction
Cohen Reductive Lithiation
Combes Quinoline Synthesis
Conrad-Limpach Quinoline Synthesis
Cope Elimination
Cope Rearrangement
Corey-Bakshi-Shibata Reduction
Corey-Chaykovsky Epoxidation
Corey-Fuchs Reaction
Corey-Gilman-Ganem Oxidation
Corey-Kim Oxidation
Corey-Kwiatkowski Reaction
Corey-Link Reaction
Corey-Schmidt Oxidation
Corey-Suggs Oxidation
Corey-Winter Olefination
Cornforth Rearrangement
Craig 2-Bromo-Pyridine Synthesis
Cram's Rule
Criegee Glycol Oxidation
Criegee Ozonolysis
Criegee Rearrangement
Crum-Brown-Gibson Substitution Rule
Curtius Rearrangement
[m+n(+. . . )] Cycloaddition
[2+2] Cycloaddition
Dakin Reaction
Dakin-West Reaction
Danheiser Annulation
Darzens Condensation
Darzens Halogenation
Darzens Olefin Acylation
Darzens-Nenitzescu Reaction
Davidson Oxazole Cyclization
de Mayo Reaction
Decker-Becker Secondary Amine Synthesis
Del´epine Reaction
Demjanov Rearrangement
Dess-Martin Periodinane Oxidation
D-Homo Rearrangement
Dieckmann Condensation
Diels-Alder Reaction
Diels-Reese Reaction
Dienol-Benzene Rearrangement
Dienone-Phenol Rearrangement
Dimroth Rearrangement
Di-¿-Methane Rearrangement
1,3-Dipolar Cycloaddition
Doebner Reaction
Doebner-Miller Reaction
Doering-Moore-Skattebøl Reaction
Dotz Benzannulation
Dowd-Beckwith Ring Expansion
Duff Reaction
Dutt-Wormall Reaction
Eastwood Olefination
Eder Reaction
Edman Degradation
Eglinton Coupling
Ehrlich-Sachs Reaction
Einhorn Acylation
Einhorn-Brunner Reaction
Eisleb Alkylation
Elbs Persulfate Oxidation
Elbs Reaction
Eltekoff Hydrolysis
Emde Degradation
Emmert Reaction
Erlenmeyer-plochl Azlactone Synthesis
Eschenmoser Coupling
Eschenmoser Fragmentation
Eschweiler-Clarke Methylation
Ester Pyrolysis
E´ tard Reaction
Evans Aldol Reaction
Favorskii Rearrangement
Favorskii-Babayan Reaction
Feist-Benary Reaction
Fenton Reaction
Ferrier Reaction
Ferrier-II Rearrangement
F´etizon Oxidation
Finkelstein Reaction
Fischer Carbene Complexes
Fischer Indole Synthesis
Fischer Oxazole Synthesis
Fischer Phenylhydrazine Synthesis
Fischer Phenylhydrazone and Osazone Synthesis
Fischer-Helferich Glycosylation
Fischer-Hepp Rearrangement
Fischer-Speier Esterification
Fischer-Tropsch Synthesis
Fleming-Tamao Oxidation
Flood Reaction
Forster Reaction
Franchimont Condensation
Frankland Reaction
Fr´ater-Seebach Alkylation
Freund Reaction
Friedel-Crafts Acylation
Friedel-Crafts Alkylation
Friedl¿ander Condensation
Fries Rearrangement
Fritsch-Buttenberg-Wiechell Rearrangement
Fujimoto-Belleau Reaction
Fukuyama Amine Synthesis
Fukuyama Indole Synthesis
F¿urstner Indole Synthesis
Gabriel Primary Amine Synthesis
Gabriel Reaction
Gabriel-Colman Rearrangement
Garner Aldehyde
Gassman Indole Synthesis
Gassman Oxindole Synthesis
Gassman Reaction
Gattermann Aldehyde Synthesis
Gattermann Reaction
Gattermann-Koch Formylation
Gewald Reaction
Ghosez Cyclization
Ghosez Keteniminium-Olefin Cyclization
Gibbs-Wohl Naphthalene Oxidation
Gilman-Cason Ketone Synthesis
Gilman-Speeter Reaction
Gomberg Free Radical Reaction
Gomberg-Bachmann Pinacol Synthesis
Gomberg-Bachmann Reaction
Gould-Jacobs Reaction
Graebe-Ullmann Synthesis
Gr¿anacher Synthesis
Gribble Reductive Amination
Griess Diazotization
Grignard Degradation
Grignard Reaction
Grob Fragmentation
Grosheintz-Fischer-Reissert Aldehyde Synthesis
Grundmann Aldehyde Synthesis
Gryszkiewicz-Trochimowski and Mccombie Fluorination
Guareschi Reaction
Guerbet Condensation
Gutknecht Condensation
Hajos-Parrish-Eder-Sauer-Wiechert Reaction
Haller-Bauer Cleavage
Hammick Reaction
Hansley-Prelog Acyloin Condensation
Hantzsch Dihydropyridine Synthesis
Hantzsch Pyrrole Synthesis
Hantzsch Thiazole Synthesis
Hass-Bender Oxidation
Haworth Methylation
Haworth Synthesis
Hayashi Rearrangement
Heck Reaction
Hegedus Indole Synthesis
Helferich Condensation
Helferich Glycosylation
Hell-Volhard-Zelinsky Reaction
Hemetsberger Indole Synthesis
Henkel Reaction
Henry Reaction
Herbst-Engel Transamination
Heron Rearrangement
Herz Reaction
Heumann Indigo Process
Heyns Rearrangement
Hilbert-Johnson Reaction
Hinsberg Oxindole Synthesis
Hinsberg Reaction
Hinsberg Sulfone Synthesis
Hinsberg Thiophene Synthesis
Hiyama Coupling
Hoch-Campbell Reaction
Hock Rearrangement
Hofer-Moest Reaction
Hofmann Degradation
Hofmann Elimination
Hofmann Isonitrile Synthesis
Hofmann Rule
Hofmann-Loffler-Freytag Reaction
Hofmann-Martius Rearrangement
Hofmann-Sand Reaction
Hooker Oxidation
Horenstein-P¿ahlicke Reaction
Horner-Wadsworth-Emmons Olefination
Hosomi-Sakurai Allylation
Houben-Hoesch Reaction
Houdry Cracking Process
Huisgen Pyrrole Synthesis
Hunsdiecker Condensation
Hunsdiecker Reaction
Hydroformylation
Iodolactonization
Irvine-Purdie Methylation
Jacobsen Rearrangement
Jacobsen-Katsuki Epoxidation
Janovsky Reaction
Japp-Klingemann Fischer Indole Synthesis
Japp-Klingemann Reaction
Japp-Maitland Condensation
Johnson Orthoester Claisen Rearrangement
Jones Oxidation
Jourdan-Ullmann Reaction
Julia Olefination
Juli´a-Colonna Asymmetric Epoxidation
Kabachnik-Fields Reaction
Kahne Glycosylation
Keck Allylation
Keck Macrolactonization
Kemp Elimination
Kennedy Oxidative Cyclization
Kiliani-Fischer Cyanohydrin Synthesis
Kishner Decomposition
Knoevenagel Condensation
Knoevenagel Diazotization Method
Knorr Pyrazole Synthesis
Knorr Pyrrole Synthesis
Knorr Quinoline Synthesis
Koch-Haaf Carboxylation
Kochi Reaction
Koenigs-Knorr Reaction
Kolbe Electrolysis
Kolbe Nitrile Synthesis
Kolbe-Schmidt Reaction
Kondrat'eva Pyridine Synthesis
Kornblum Oxidation
Kornblum-Delamare Rearrangement
Kostanecki-Robinson Reaction
Kowalski Ester Homologation
Krapcho Decarboxylation
Kriewitz Condensation
Kr¿ohnke Pyridine Synthesis
Kuhn-Roth Oxidation
Kuhn-Winterstein Reduction
Kulinkovich Cyclopropanation
Kutscheroff Acetylene Hydration
Lander Rearrangement
Larock Indole Synthesis
Lawesson's Reagent
Lebedev Process
Lehmstedt-Tanasescu Reaction
Lemieux-Johnson Oxidation
Leuckart Reaction
Leuckart Thiophenol Synthesis
Levinstein Process
Lieben Iodoform Reaction
Liebeskind-Srogl Cross-Coupling
Lindlar Hydrogenation
Lobry de Bruyn-Alberda van Ekenstein Transformation
Lombardo Methylenation
Lossen Rearrangement
Luche Reaction
Luche Reduction
MacDonald-Fischer Degradation
Madelung Indole Synthesis
Maillard Reaction
Maitland-Japp Reaction
Majetich Annulation
Malaprade Reaction
Malonic Ester Synthesis
Mandelic Acid Synthesis
Mannich Reaction
Marckwald Asymmetric Synthesis
Markownikoff Rule and Anti-Markownikoff Rule
Martinet Reaction
Martin's Sulfurane
Mattox-Kendall Reaction
McCormack Cycloaddition
McFadyen-Stevens Reaction
McLafferty Rearrangement
McMurry Coupling
Meerwein Arylation
Meerwein-Ponndorf-Verley Reduction
Meerwein's Salt
Meinwald Rearrangement
Meisenheimer Complexes
Meisenheimer Rearrangement
Menke Nitration
Menschutkin Reaction
Mentzer Pyrone Synthesis
Merrifield Solid-Phase Peptide Synthesis
Meyer-Hartmann Reaction
Meyers Aldehyde Synthesis
Meyer-Schuster Rearrangement
Michael Addition
Michaelis-Arbuzov Rearrangement
Michael-Stetter Reaction
Miescher Degradation
Mignonac Reaction
Milas Hydroxylation
Mislow-Evans Rearrangement
Mitsunobu Reaction
Moffatt-Swern Oxidation
Moore Cyclization
Morgan-Walls Cyclization
Mori-Ban Indole Synthesis
Morin Rearrangement
Mosher's Acid
Moureau-Mignonac Ketimine Synthesis
Mukaiyama Aldol Reaction
Mukaiyama-Michael Reaction
M¿ uller-Cunradi-Pieroh Process
Myers-Saito Cyclization
Nagata Reaction
Nazarov Cyclization
Neber Rearrangement
Neber-Bossel Synthesis
Nef Reaction
Negishi Cross-Coupling
Nencki Reaction
Nenitzescu Synthesis
Nenitzescu Indole Synthesis
Newman-Kwart Rearrangement
Nicholas Reaction
Niementowski Reaction
Nierenstein Reaction
Norrish Type I Reaction
Norrish Type II Reaction
Noyori Hydrogenation
Nozaki-Hiyama-Kishi Reaction
Nysted Reagent
Ohle Quinoxaline Synthesis
Oppenauer Oxidation
Orton Rearrangement
Ostromislensky Process
Overman Rearrangement
Paal-Knorr Furan Synthesis
Paal-Knorr Pyrrole Synthesis
Paneth Technique
Parham Cyclization
Parikh-Doering Oxidation
Passerini Reaction
Paterno-Buchi Reaction
Pauson-Khand Reaction
Payne Rearrangement
Pearlman's Catalyst
Pechmann Pyrazole Synthesis
Pechmann Reaction
Pellizzari Reaction
Perkin Reaction
Perkin Synthesis
Perkow Reaction
Petasis-Ferrier Rearrangement
Peterson Olefination
Petrenko-Kritschenko Piperidone Synthesis
Pfau-Plattner Azulene Synthesis
Pfitzinger Reaction
Pfitzner-Moffatt Oxidation
Phillips-Ladenburg Benzimidazole Synthesis
Photo-Fries Rearrangement
Pictet-Gams Synthesis
Pictet-Spengler Reaction
Piloty-Robinson Pyrrole Synthesis
Pinacol Coupling Reaction
Pinacol Rearrangement
Pinner Condensation
Pinner Reaction
Pinner S-Triazine Synthesis
Piria Reaction
Plancher Rearrangement
Polonovski Reaction
Pomeranz-Fritsch Reaction
Ponzio Reaction
Pr´evost Reaction
Prey Ether Cleavage
Prilezhaev Reaction
Prins Reaction
Pudovik Reaction
Pummerer Rearrangement
Quelet Reaction
Radziszewski Reaction
Ramberg-B¿acklund Reaction
Raney Nickel
Rauhut-Currier Reaction
Reed Reaction
Reformatsky Reaction
Regitz Diazo Transfer
Reilly-Rickinbottom Rearrangement
Reimer-Tiemann Reaction
Reissert Compound
Reissert Indole Synthesis
Reppe Alkyne Cyclotrimerization
Reppe Carbonylation
Reppe Cyclization
Reppe Vinylation
Retro-Diels-Alder Reaction
Retro-Ene Reaction
Retropinacol Rearrangement
Reverdin Rearrangement
Riehm Quinoline Synthesis
Rieke Metal
Riemenschneider Reaction
Riley Oxidation
Ritter Reaction
Robinson Annulation
Robinson-Gabriel Oxazole Synthesis
Robinson-Schopf Condensation
Rosenmund Reaction
Rosenmund Reduction
Rosenmund-von Braun Reaction
Rothemund Reaction
Roush Crotylboration
Rowe Rearrangement
Rubottom Oxidation
Ruff Degradation
Rupe Rearrangement
Sabatier-Senderens Reduction
Saegusa Cyclization
Saegusa Oxidation
Sandmeyer Isatin Synthesis
Sandmeyer Reaction
Sarett Oxidation
Saytzeff Rule
Schiff Base
Schlack-Kumpf Reaction
Schlotterbeck Reaction
Schmidlin Ketene Synthesis
Schmidt Glycosylation
Schmidt Reaction
Schmidt-Rutz Reaction
Schmittel Cyclization
Scholl Reaction
Sch¿ollkopf Bis-Lactim Ether Method
Sch¿ollkopf Oxazole Synthesis
Sch¿onberg Rearrangement
Schotten-Baumann Reaction
Schwartz Reagent
Screttas Lithiation
Selenoxide Elimination
Semmler-Wolff Aromatization
Serini Reaction
Seyferth-Gilbert Homologation
Shapiro Reaction
Sharpless Aminohydroxylation
Sharpless Dihydroxylation
Sharpless Epoxidation
Shechter-Kaplan Oxidative Nitration
Shi Epoxidation
Simmons-Smith Reaction
Simonini Reaction
Skraup Reaction
Smiles Rearrangement
Sommelet Reaction
Sommelet-Hauser Rearrangement
Sonn-Muller Reaction
Sonogashira Coupling
Staudinger [2+2] Cycloaddition
Staudinger Reaction
Stec Reaction
Steglich Catalyst
Steglich Rearrangement
Stephen Reaction
Stetter Reaction
Stevens Rearrangement
Stieglitz Rearrangement
Stille Coupling
Stobbe Condensation
Stolle-Becker Synthesis
Stork Reaction
Strecker Degradation
Strecker Reaction
Strecker Synthesis
Su´arez Cleavage
Sugasawa Indole Synthesis
Sugasawa Reaction
Sundberg Indole Synthesis
Suzuki Coupling
Swarts Reaction
Takai Olefination
Tebbe Olefination
ter Meer Reaction
Thiele-Winter Acetoxylation
Thorpe-Ziegler Cyclization
Tiemann Cyanohydrin Amination
Tiemann Rearrangement
Tiffeneau-Demjanov Ring Expansion
Tishchenko Reaction
Traube Purine Synthesis
Trofimov Reaction
Trost Desymmetrization
Truce-Smiles Rearrangement
Tscherniac-Einhorn Reaction
Tsuji-Trost Reaction
Twitchell Process
Tyrer Process
Ueno-Stork Cyclization
Ugi Reaction
Ullmann Acridine Synthesis
Ullmann Coupling
Ullmann Diaryl Ether Synthesis
Urech Cyanohydrin Method.Synthesis
van Slyke Method
Varrentrapp Reaction
Victor Meyer Reaction
Vilsmeier Formylation
Vinylcyclopropane Rearrangement
Voigt Reaction
von Auwers Rearrangement
von Braun Cyanogen Bromide Reaction
von Braun Degradation
von Braun-Rudolf Synthesis
von Richter Cinnoline Synthesis
von Richter Reaction
Vorbr¿uggen Glycosylation
Wacker Oxidation
Wagner-Jauregg Reaction
Wagner-Meerwein Rearrangement
Walden Inversion
Wallach Rearrangement
Weerman Reaction
Weidenhagen Synthesis
Weinreb Amide Formation
Weinreb Ketone Synthesis
Weiss-Cook Condensation
Weitz-Scheffer Epoxidation
Wender Indole Synthesis
Wessely-Moser Rearrangement
Westphalen Rearrangement
Wharton Rearrangement
Wibaut-Arens Alkylation
Wichterle Reaction
Widman-Stoermer Synthesis
Wilkinson's Catalyst
Willgerodt-Kindler Reaction
Williamson Ether Synthesis
Wittig Reaction
[1,2]-Wittig Rearrangement
[2,3]-Wittig Rearrangement
Wohl Degradation
Wohl-Aue Reaction
W¿ohler Synthesis
Wohl-Ziegler Bromination
Wolff Rearrangement
Wolffenstein-B¿oters Reaction
Wolff-Kishner Reduction
Woodward Cis-Hydroxylation
Wurtz Synthesis
Wurtz-Fittig Reaction
Yamada Coupling
Yamaguchi Esterification
Zeisel Determination
Zelinsky-Stadnikoff Reaction
Zempl´en Deacetylation
Zerewitinoff Determination
Ziegler Alcohol Synthesis
Ziegler-Hafner Azulene Synthesis
Ziegler-Natta Polymerization
Zimmermann Reaction
Zincke Disulfide Cleavage
Zincke Nitration
Zincke Reaction
Zincke-Suhl Reaction
Zinke Synthesis
Appendixes
Schematic Reaction Index
Reaction Type Summary
Summary of Initial Publications on Named Reactions
Journal Abbreviation
The Statistics of Reaction Published Years
Subject Index
Table of Contents provided by Publisher. All Rights Reserved.

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