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Tautomerism in C=O and C=NR Systems C=O Enolization with Metal Amide Bases C=O Enolization: Kinetic Acidities Mild Methods for Enolate Generation Enolate Structure: A Survey of X-ray Structures
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Reading Assignment for week Olefin Addition Reactions: Part–3 Chemistry 206 Advanced Organic Chemistry
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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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Woodward-Hoffmann Theory R. B. Woodward and R. Hoffmann, The Conservation of Orbital Symmetry, Verlag Chemie, Weinheim, 1970. Frontier Molecular Orbital Theory I. Fleming, Frontier Orbitals and Organic Chemical Reactions
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Advanced Organic Chemistry Handout–10A Diastereoselective Attack of Electrophiles on Chiral Olefins Matthew D. Shair Wednesday
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Carey & Sundberg: Part A; Chapter 7 Carbanions & Other Nucleophilic Carbon Species
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1. Type II Diels-Alder II. Radical Reactions A. 5-Exo- and 6-Endo- Ring Formations
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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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Carbenes are Accessible via Sigmatropic Rearrangement
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Intramolecular Enone-Olefin Photocycloadditions Directed Toward Natural Product Synthesis Travis Dunn DAE Group Friday Afternoon Seminar
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