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1 Acetoacetic ester synthesis. 2 Aldol condensation. 3 Alkene metathesis. 4 Bayer-Villiger oxidation. 5 Birch reduction. 6 Claisen condensation.
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(Sources: Vollhardt/Schore, Textbook, and Lecture Notes) 1 Acetoacetic ester synthesis 2 Aldol condensation 3 Alkene metathesis 4 Bayer-Villiger oxidation 5 Birch reduction 6 Claisen condensation 7 Claisen rearrangement 8 Clemmensen reduction 9 Cope rearrangement 10 Dieckmann condensation 11 Diels-Alder reaction 12 Friedel-Crafts reaction 13 Gabriel synthesis 14 Grignard reaction 15 Heck coupling 16 Hydroboration reaction 17 Malonic ester synthesis 18 Mannich reaction 19 Michael addition 20 Ozonolysis 21 Sharpless Dihydroxylation 22 Sharpless Epoxidation 23 Simmons-Smith reaction 24 Sonogashira coupling 25 Stille coupling 26 Strecker synthesis of amino acids 27 Suzuki coupling 28 Wadsworth-Emmons reaction 29 Williamson ether synthesis 30 Wittig reaction Dr. P. Wipf Page 1 of 1 11/18/