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1;Thieme: Science of Synthesis Knowledge Updates 2017/1;12;Title Page;63;Copyright;84;Preface;95;Abstracts;116;Science of Synthesis Knowledge Updates 2017/1;217;Table of Contents;238;3.6.16 Gold-Catalyzed Cycloaddition Reactions;378.1;3.6.16.1 Cycloadditions via Gold-Containing 1,n-Dipolar Intermediates;378.1.1;3.6.16.1.1 Method 1: Gold-Containing Benzopyrylium Intermediates;388.1.1.1;3.6.16.1.1.1 Variation 1: Gold-Containing Benzopyrylium Azomethine Ylides;448.1.1.2;3.6.16.1.1.2 Variation 2: Gold-Containing 2-Oxoalkyl Oxonium Species;478.1.2;3.6.16.1.2 Method 2: Furyl-Gold 1,n-Dipole Intermediates;488.1.2.1;3.6.16.1.2.1 Variation 1: Furyl-Gold 1,3-Dipole Intermediates;488.1.2.2;3.6.16.1.2.2 Variation 2: Furyl-Gold 1,4-Dipole Intermediates;518.1.2.3;3.6.16.1.2.3 Variation 3: Furan-Based ortho-Quinodimethane Intermediates;548.1.3;3.6.16.1.3 Method 3: Gold-Containing All-Carbon 1,3-Dipoles;558.2;3.6.16.2 Cycloadditions via Gold-Coordinated Allene Intermediates;578.2.1;3.6.16.2.1 Method 1: Cycloadditions Initiated by Gold Activation of Allenes;578.2.2;3.6.16.2.2 Method 2: Cycloadditions Initiated by Gold Activation of Propargylic Carboxylates;698.3;3.6.16.3 Cycloadditions via trans-Alkenylgold Intermediates;718.3.1;3.6.16.3.1 Method 1: trans-Alkenylgold Intermediates Generated by Alkyne Activation;718.3.1.1;3.6.16.3.1.1 Variation 1: Alkynes as Latent Alkenes in Gold-Catalyzed Cycloadditions;748.4;3.6.16.4 Cycloadditions via Gold Carbene Intermediates;768.4.1;3.6.16.4.1 Method 1: Gold Carbenes Generated by Cycloisomerization of Alkynes and Alkenes;768.4.2;3.6.16.4.2 Method 2: Gold Carbenes Generated by 1,2-Acyloxy Migration of Propargyl Carboxylates;818.4.3;3.6.16.4.3 Method 3: Gold Carbenes Generated by Alkyne Oxidation;848.4.3.1;3.6.16.4.3.1 Variation 1: Gold-Catalyzed Cycloaddition Reactions by Nitrene Transfer;878.4.3.2;3.6.16.4.3.2 Variation 2: Gold-Catalyzed Cycloaddition Reactions by Carbene Transfer;888.4.4;3.6.16.4.4 Method 4: Gold Carbenes Generated by Diazo Decomposition;898.5;3.6.16.5 Cycloadditions via Gold-Coordinated Heteroatom Intermediates;919;4.4.7 Product Subclass 7: Silylboron Reagents;1019.1;4.4.7.1 Synthesis of Product Subclass 7;1049.1.1;4.4.7.1.1 Preparation by Si-B Bond Formation;1049.1.1.1;4.4.7.1.1.1 Method 1: Nucleophilic Substitution at Boron with Silyllithium Reagents;1049.1.1.1.1;4.4.7.1.1.1.1 Variation 1: Substitution of Amino-Substituted Chloroboranes;1049.1.1.1.2;4.4.7.1.1.1.2 Variation 2: Substitution of a Diaryl-Substituted Fluoroborane;1059.1.1.1.3;4.4.7.1.1.1.3 Variation 3: Nucleophilic Substitution of Diol-Substituted Hydro- or Alkoxyboranes;1069.1.1.2;4.4.7.1.1.2 Method 2: Iridium-Catalyzed Borylation of Trialkylsilanes;1079.1.1.3;4.4.7.1.1.3 Method 3: Reductive Coupling of Chlorosilanes and Chloroboranes;1089.1.2;4.4.7.1.2 Modification of Si-B Substitution Pattern;1099.1.2.1;4.4.7.1.2.1 Method 1: Ligand Exchange at the Boron Atom;1099.1.2.2;4.4.7.1.2.2 Method 2: Manipulation at the Silicon Atom;1119.2;4.4.7.2 Applications of Product Subclass 7 in Organic Synthesis;1139.2.1;4.4.7.2.1 Method 1: Reactions with Alkynes;1139.2.1.1;4.4.7.2.1.1 Variation 1: Transition-Metal-Catalyzed Silaboration;1139.2.1.2;4.4.7.2.1.2 Variation 2: Palladium-Catalyzed Silaborative Cyclization;1199.2.1.3;4.4.7.2.1.3 Variation 3: Nickel-Catalyzed Silaborative Dimerization;1209.2.1.4;4.4.7.2.1.4 Variation 4: Palladium-Catalyzed (2 + 2 + 1) Cycloaddition with Silylenes;1219.2.1.5;4.4.7.2.1.5 Variation 5: Copper-Catalyzed Silylation;1229.2.2;4.4.7.2.2 Method 2: Reactions with Alkenes;1279.2.2.1;4.4.7.2.2.1 Variation 1: Platinum-Catalyzed Silaboration;1279.2.2.2;4.4.7.2.2.2 Variation 2: Base-Catalyzed Silaboration;1319.2.2.3;4.4.7.2.2.3 Variation 3: Photochemical Radical Silylation;1329.2.3;4.4.7.2.3 Method 3: Reactions with Conjugated Dienes and Enynes;1339.2.3.1;4.4.7.2.3.1 Variation 1: Transition-Metal-Catalyzed 1,4-Silaboration;1339.2.3.2;4.4.7.2.3.2 Variation