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一.反应的类型 二.反应机理 1.E1机理 2.单分子共轭碱消除(E1CB机理 CB) 3.E2机理
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一、诱导效应 结构特征( 传递方式 传递强度 相对强度 二.共轭体系 1.共轭体系与共轭效应
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The Synthetic Applications of Carbonyl Ylides David M. Barnes Evans Group Seminars, March 16, 1993 Reviews - Ylides Padwa, A.; Hornbuckle, S. F. Chem. Rev. 1991, 91, 263-309. Padwa, A.; Krumpe, K. E. Tetrahedron. 1992, 48, 5385-5483
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Advanced Organic Chemistry Handout–10A Diastereoselective Attack of Electrophiles on Chiral Olefins Matthew D. Shair Wednesday
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Hoffmann, Angew. Chem. Int. Ed. 1979, 18, 563-572 (Stereochemistry of) Nakai, Chem. Rev. 1986, 86, 885-902 (Wittig Rearrangement) Evans, Accts. Chem. Res. 1974, 7, 147-55 (Sulfoxide Rearrangement)
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Enantioselective Carbonyl Addition Handout
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Carbonyl and Azomethine Electrophiles-1 Relevant Dunitz Articles Geometrical Reaction Coordinates. Il. Nucleophilic Addition to Reactivity Trends
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Other Useful References Polyketide Biosynthesis Historical Perspective on the Aldol Reaction Aldol Diastereoselectivity Enolate Diastereoface Selectivity Absolute Control in the Aldol Process
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An Organizational Format for the Classification of Functional Groups. Applications to the Construction of Difunctional Relationships
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D. A. Evans Enolate Acylation Acylation & Carboxylation Chem 206 The Reaction: Acylation + Carboalkoxylation + Situations where the reaction is employed:
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