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Organic Synthesis
- 3. Retrosynthetic analysis Disconnection of T.M. Intermediate Starting material Synthesis tree
- 7. Major Ionic Reactions for Carbon
- 9. Rearrangements Useful in Synthesis
- 13. Organometallic and Ylide Methods of Carbon-Carbon Bond Formation
- 14. Stereochemistry of Grignard Addition
- 15. Orthometallation Cross Coupling (Suzuki Rxn 1,4-Addition
- 17. Wittig Reaction
- 18. Carbonyl Activation and Enolate Chemistry in Carbon-Carbon Bond Formation
- 20. Regiospecificity in Enol Ether Formation
- 22. Alkylation of Carbanion CH 3 -OSO 2 F methyl fluorosulfonate oxirane (epoxide) CH 3 -OSO 2 O-CH 3 dimethyl sulfate (R-OTs) toluene-p-sulfonates (or tosylates) R-OSO 2 CH 3 (R-OMs) methanesulfnates (or mesylates) R-X alkyl halide Structure Alkylating agent
- 26. Michael Addition
- 27. 4. Robinson annulation - a special class of Michael additions which lead to one six-membered ring fused to another
- 29. General Pattern of Reduction
- 30. Reductions with Hydride Reagents
- 35. Retrosynthesis
- 36. Synthesis