中国科学院大学-高等有机化学-第五章-碳-碳多重键，羰基和其他官能团的还原-Reduction of Carbon-Carbon Multiple Bonds, Carbonyl Groups, and Other Functional Groups.ppt

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中国科学院大学-高等有机化学-第五章-碳-碳多重键，羰基和其他官能团的还原-Reduction of Carbon-Carbon Multiple Bonds, Carbonyl Groups, and Other Functional Groups.ppt

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5.5. Reduction Reactions Involving Hydrogen Atom Donors 5.6. Dissolving-Metal Reductions 5.6.1. Addition of Hydrogen 5.6.1.1. Reduction of Ketones and Enones 5.6.1.2. Dissolving-Metal Reduction of Aromatic Compounds and Alkynes. Birch Reduction 5.6.2. Reductive Removal of Functional Groups 1 2 5.6.2. Reductive Removal of Functional Groups 3 5.6.2. Reductive Removal of Functional Groups 5.6.2. Reductive Removal of Functional Groups 5.6.2. Reductive Removal of Functional Groups 5.7.1. Reductive Deoxygenation of Carbonyl Groups to Methylene 5.7.2. Reduction of Carbonyl Compounds to Alkenes 5.8. Reductive Elimination and Fragmentation Chapter 6. Concerted Cycloadditions, Unimolecular Rearrangements, and Thermal Eliminations Nov. 20th, 2008 6.1. Diels-Alder Reactions 6.1.1. The Diels-Alder Reaction: General Features 6.1.2. Substituent Effects on the Diels-Alder Reaction 6.1.2. Substituent Effects on the Diels-Alder Reaction 6.1.2. Substituent Effects on the Diels-Alder Reaction 6.1.2. Substituent Effects on the Diels-Alder Reaction 6.1.2. Substituent Effects on the Diels-Alder Reaction 6.1.3. Lewis Acid Catalysis of the Diels-Alder Reaction 6.1.3. Lewis Acid Catalysis of the Diels-Alder Reaction 6.1.3. Lewis Acid Catalysis of the Diels-Alder Reaction-Catalyst 5.3.2.3. Chelation Control. 5.3.2.3. Chelation Control. 5.3.2.3. Chelation Control. 5.3.2.3. Chelation Control. 5.3.3. Enantioselective Reduction of Carbonyl Compounds 5.3.3.1. Reduction with Chiral Boranes 5.3.2.3. Chelation Control. 5.2. Catalytic Hydrogenation of Carbonyl and Other Functional Groups 5.2. Catalytic Hydrogenation of Carbonyl and Other Functional Groups 5.2. Catalytic Hydrogenation of Carbonyl and Other Functional Groups 5.3. Group III Hydride-Donor Reagents 5.3.1. Comparative Reactivity of Common Hydride Donor Reagents 5.3.1. Comparative Reactivity of Common Hydride Donor Reagents 5.3.1. Comparative Reactivity of Common Hydride Donor Reagents 5.3.1.1. Partial Reduction of Carboxylic Acid Derivati