1;Science of Synthesis: Asymmetric Organocatalysis 2 - Brønsted Base and Acid Catalysts, and Additional Topics;11.1;Organizational Structure of Science of Synthesis;21.2;Science of Synthesis Reference Library;31.3;Title page;51.4;Imprint;71.5;Preface;81.6;Asymmetric Organocatalysis Volumes;101.7;Abstracts;121.8;Overview;241.9;Table of Contents;261.10;2.1 Brønsted Bases;481.10.1;2.1.1 Chiral Guanidine and Amidine Organocatalysts;481.10.1.1;2.1.1.1 Synthesis of 2-Aminoacetonitriles;491.10.1.1.1;2.1.1.1.1 Catalytic Asymmetric Strecker Reactions;491.10.1.2;2.1.1.2 Synthesis of Chiral Alcohols;501.10.1.2.1;2.1.1.2.1 Catalytic Nitroaldol (Henry) Reactions;501.10.1.2.1.1;2.1.1.2.1.1 Nitroaldol Reactions with a-Chiral Aldehydes;531.10.1.2.1.2;2.1.1.2.1.2 Nitroaldol Reactions with a-Keto Esters;541.10.1.2.2;2.1.1.2.2 Catalytic Asymmetric Aldol Reactions;551.10.1.2.2.1;2.1.1.2.2.1 Aldol Reactions with Dihalofuran-2(5H)-ones;571.10.1.3;2.1.1.3 Synthesis of Chiral Amines;591.10.1.3.1;2.1.1.3.1 Catalytic Asymmetric Nitro-Mannich-Type Reactions;591.10.1.3.1.1;2.1.1.3.1.1 Nitro-Mannich-Type Reactions with Nitroacetates;631.10.1.3.1.2;2.1.1.3.1.2 Nitro-Mannich-Type Reactions with a-Substituted Nitroacetates;641.10.1.3.2;2.1.1.3.2 Catalytic Asymmetric Mannich-Type Reactions;651.10.1.4;2.1.1.4 Synthesis of Chiral Nitroalkanes;671.10.1.4.1;2.1.1.4.1 Catalytic Asymmetric Michael Reactions;671.10.1.4.1.1;2.1.1.4.1.1 Michael Reactions with ß-Keto Esters;691.10.1.4.1.2;2.1.1.4.1.2 Michael Reactions with Phenols;711.10.1.4.1.3;2.1.1.4.1.3 Michael Reactions with Nitroalkanes;721.10.1.4.1.4;2.1.1.4.1.4 Michael Reactions with 4,7-Dihydroindoles;731.10.1.5;2.1.1.5 Synthesis of Chiral Epoxy Ketones;751.10.1.5.1;2.1.1.5.1 Catalytic Asymmetric Nucleophilic Epoxidation Reactions;751.10.1.6;2.1.1.6 Synthesis of Chiral Hydrazines;761.10.1.6.1;2.1.1.6.1 Catalytic Asymmetric Amination Reactions;761.10.1.7;2.1.1.7 Synthesis of Chiral Phosphonates and Phosphine Oxides;781.10.1.7.1;2.1.1.7.1 Catalytic Asymmetric 1,4-Addition Reactions;781.10.1.7.1.1;2.1.1.7.1.1 1,4-Addition Reactions with Phosphites;781.10.1.7.1.2;2.1.1.7.1.2 1,4-Addition Reactions with Phosphine Oxides;791.10.1.8;2.1.1.8 Synthesis of Chiral d-Lactones;801.10.1.8.1;2.1.1.8.1 Catalytic Asymmetric Inverse-Electron-Demand Hetero-Diels--Alder Reactions;801.10.1.9;2.1.1.9 Synthesis of Chiral Pyrrolidines;831.10.1.9.1;2.1.1.9.1 Catalytic Asymmetric [3 + 2]-Cycloaddition Reactions;831.10.1.10;2.1.1.10 Synthesis of Chiral a-Keto Esters;841.10.1.10.1;2.1.1.10.1 Catalytic Asymmetric Claisen Rearrangement Reactions;841.10.2;2.1.2 Cinchona Alkaloid Organocatalysts;881.10.2.1;2.1.2.1 Nucleophilic Catalysis;891.10.2.1.1;2.1.2.1.1 Asymmetric Reactions with Ketenes;901.10.2.1.1.1;2.1.2.1.1.1 Synthesis of ß-Lactones;901.10.2.1.1.2;2.1.2.1.1.2 Intramolecular Synthesis of ß-Lactones;911.10.2.1.1.3;2.1.2.1.1.3 Synthesis of ß-Lactams;921.10.2.1.1.4;2.1.2.1.1.4 Synthesis of ß-Oxo Amides;931.10.2.1.1.5;2.1.2.1.1.5 Asymmetric Synthesis of a-Halogenated Esters;941.10.2.1.1.6;2.1.2.1.1.6 Cycloaddition of Ketenes and N-Thioacylimines;951.10.2.1.2;2.1.2.1.2 Asymmetric Morita--Baylis--Hillman Reactions;961.10.2.1.2.1;2.1.2.1.2.1 Synthesis of Hydroxy Acrylates;971.10.2.1.2.2;2.1.2.1.2.2 Synthesis of Sulfonamido Enones;981.10.2.1.3;2.1.2.1.3 Enantioselective Protonation;991.10.2.1.3.1;2.1.2.1.3.1 Thiol Addition to Alkyl(silyl)ketenes;991.10.2.1.4;2.1.2.1.4 Asymmetric Cyanation of Simple Ketones;1001.10.2.1.4.1;2.1.2.1.4.1 Synthesis of Cyanohydrin Carbonates;1001.10.2.1.5;2.1.2.1.5 Asymmetric Conjugate Additions;1011.10.2.1.5.1;2.1.2.1.5.1 Synthesis of tert-Butyl Cyclopropanecarboxylates;1021.10.2.1.5.2;2.1.2.1.5.2 Reaction of Indole with Morita--Baylis--Hillman Adducts;1021.10.2.1.5.3;2.1.2.1.5.3 Reaction of Furan-2-ones with Morita--Baylis--Hillman Adducts;1031.10.2.1.6;2.1.2.1.6 Asymmetric Electrophilic Halo