This comprehensive text presents a critical discussion of the scopes and limitations of various organic synthetic methodologies that are available for performing asymmetric transformations. In addition to purely chemical methods, the book covers applications of new enzymes and other biological systems that are increasingly useful in asymmetric methodology.Introduction Nomenclature Why Asymmetric Synthesis? Methods to Achieve Asymmetric Synthesis Resolution A Question of Scale General Rules Carbonyl Additions Houk's Rule Allylic Strain Baldwin's Rules Pericyclic Transition States One-Carbon Transformations Inversions at a Single Carbon Center Chiral Organometallic Reagents Other Reactions Reactions With Carbonyl Compounds Reactions of Carbonyl Compounds With Nucleophiles Acetal Reactions Other Electrophiles Other Reactions Reductions Enolate Reactions of Carbonyl Compounds Enol Ethers and Enolate Formation Reactions of Enol Ethers and Enolates Use of Nitrogen Derivatives Asymmetric Deprotonations and Protonations Reactions of Functionalized Carbonyl Systems Alkylations of 1,2-Functionalized Carbonyl Compounds Reductions of 1,2-Functionalized Carbonyl Compounds Alkylations of 1,3-Functionalized Carbonyl Compounds Reductions of 1,3-Functionalized Carbonyl Compounds Other Systems Aldol and Related Reactions The Aldol Reaction: Methods of Control The Aldol Reaction: The Role of Enolate Geometry and Metal Counterion The Formose Reaction Preparation and Reactions of Alkenes Alkene Synthesis Reactions of Alkenes Reactions of Functionalized Alkenes Hydrogenations Other Transition Metal Catalyzed Reactions Hydride Delivery Agents Reactions of Some Functionalized Alkenes Conjugate Additions Allyl Alkylatiol£0