Science of Synthesis: Houben-Weyl Methods of Molecular Transformations is the entirely new edition of the acclaimed reference series Houben-Weyl, the standard synthetic chemistry resource since 1909. This new edition is published in English and will comprise 48 volumes published between the years 2000 and 2008.

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1;Science of Synthesis - Volume 33: Ene--X Compounds (X = S, Se, Te, N, P);11.1;Title page;31.2;Imprint;51.3;Preface;61.4;Volume Editor's Preface;81.5;Overview;101.6;Table of Contents;141.7;Introduction;441.8;33.1 Product Class 1: Alk-1-enyl Sulfur Compounds;561.8.1;33.1.1 Product Subclass 1: Alk-1-enesulfonic Acids and Derivatives;561.8.1.1;33.1.1.1 Synthesis of Product Subclass 1;561.8.1.1.1;33.1.1.1.1 Method 1: Synthesis from 2-Chloroalkanesulfonic Acid Derivatives;561.8.1.1.2;33.1.1.1.2 Method 2: Condensations of the Carbanions of Sulfonic Acid Derivatives with Carbonyl Compounds;571.8.1.1.2.1;33.1.1.1.2.1 Variation 1: Aldol-Type Condensations and Related Processes;571.8.1.1.2.2;33.1.1.1.2.2 Variation 2: Wadsworth--Emmons Alkenation Reactions;581.8.1.1.3;33.1.1.1.3 Method 3: Cyclic Alk-1-enesulfonic Esters and Sulfonamides by Metathesis Reactions;591.8.1.1.4;33.1.1.1.4 Methods 4: Miscellaneous Syntheses of Alk-1-enesulfonic Acid Derivatives from Other Sulfur Compounds;601.8.2;33.1.2 Product Subclass 2: Alk-1-enyl Sulfones;621.8.2.1;33.1.2.1 Synthesis of Product Subclass 2;621.8.2.1.1;33.1.2.1.1 Method 1: Sulfonylation of Nucleophilic Alkenyl Reagents;621.8.2.1.2;33.1.2.1.2 Method 2: Condensation of Sulfonyl Carbanions with Carbonyl Compounds;631.8.2.1.2.1;33.1.2.1.2.1 Variation 1: Aldol-Type Condensation and Dehydration;631.8.2.1.2.2;33.1.2.1.2.2 Variation 2: Knoevenagel Condensation of Activated Sulfones;651.8.2.1.2.3;33.1.2.1.2.3 Variation 3: Condensation of Sulfinyl(sulfonyl)methanes with Aldehydes;661.8.2.1.2.4;33.1.2.1.2.4 Variation 4: Horner--Wadsworth--Emmons Alkenation of a-Sulfonyl Phosphonates;671.8.2.1.2.5;33.1.2.1.2.5 Variation 5: Peterson Alkenation of a-Silylalkyl Sulfones;691.8.2.1.3;33.1.2.1.3 Method 3: Sulfonylation of Alkenes Followed by Elimination;711.8.2.1.3.1;33.1.2.1.3.1 Variation 1: Chlorosulfenylation of Alkenes, Followed by Sulfur Oxidation and Elimination;711.8.2.1.3.2;33.1.2.1.3.2 Variation 2: Sulfonomercuration of Alkenes Followed by Demercuration;721.8.2.1.3.3;33.1.2.1.3.3 Variation 3: Selenosulfonylation of Alkenes Followed by Selenium Oxidation;731.8.2.1.3.4;33.1.2.1.3.4 Variation 4: Iodosulfonylation of Alkenes Followed by Dehydroiodination;741.8.2.1.4;33.1.2.1.4 Method 4: Sulfonylation of Alkynes;761.8.2.1.5;33.1.2.1.5 Method 5: Functionalization of Alk-1-ynyl Sulfones;771.8.2.1.5.1;33.1.2.1.5.1 Variation 1: Addition Reactions;781.8.2.1.5.2;33.1.2.1.5.2 Variation 2: Cycloaddition Reactions;801.8.2.1.6;33.1.2.1.6 Method 6: Oxidation of Alk-1-enyl Sulfides and Sulfoxides;801.8.2.1.7;33.1.2.1.7 Method 7: Functionalization of Allyl Sulfones and Derivatives;811.8.2.1.8;33.1.2.1.8 Method 8: Functionalization of Simple Alk-1-enyl Sulfones;831.8.2.1.8.1;33.1.2.1.8.1 Variation 1: a-Functionalization;831.8.2.1.8.2;33.1.2.1.8.2 Variation 2: Heck Reaction;851.8.2.1.8.3;33.1.2.1.8.3 Variation 3: Cross-Metathesis Reactions;861.8.2.1.8.4;33.1.2.1.8.4 Variation 4: Diels--Alder Reactions of Dienyl Sulfones;871.8.2.1.8.5;33.1.2.1.8.5 Variation 5: Substitution of ß-Functionalized Alk-1-enyl Sulfones;881.8.3;33.1.3 Product Subclass 3: S-Alk-1-enylsulfoximides;941.8.3.1;33.1.3.1 Synthesis of Product Subclass 3;941.8.3.1.1;33.1.3.1.1 Method 1: Condensation of Sulfonimidoyl Carbanions with Carbonyl Compounds;941.8.3.1.1.1;33.1.3.1.1.1 Variation 1: Aldol-Type Condensations of a-Sulfonimidoyl Carbanions and the Dehydration of the Intermediate ß-Hydroxylated Sulfoximides;951.8.3.1.1.2;33.1.3.1.1.2 Variation 2: Peterson and Wadsworth--Emmons Alkenation Reactions;971.8.3.1.2;33.1.3.1.2 Method 2: Imination of Alk-1-enyl Sulfoxides;981.8.3.1.3;33.1.3.1.3 Method 3: Functionalization of Simple S-Alk-1-enyl- and S-Alk-2-enylsulfoximides;991.8.4;33.1.4 Product Subclass 4: Alk-1-enesulfinic Acids and Derivatives;1021.8.4.1;33.1.4.1 Synthesis of Product Subclass 4;1021.8.4.1.1;33.1.4.1.1 Method 1: Reaction of Allenes and Alkynes