The extra-intensive summer course, Name Reactions, will be opened during this Summer from 24th July to 2nd September.
Join us? Mail me.
As for the last summer, we had happy time with many reactions, for example:
REACTION INDEX
OXIDATION
Corey-Kim Oxidation
Corey-Chaykovsky Reaction
Dess-Martin Oxidation
Jacobsen-Katsuki Epoxidation
Jones Oxidation
Oppenauer Oxidation
Pfitziner Moffatt Oxidation
Sharpless Epoxidation
Swern Oxidation
Wacker Oxidation
REDUCTION
Birch Reduction
Bouveault-Blanc Reduction
Clemmensen Reduction
Hydroboration Reaction
Meerwein-Ponndorf-Verley Reduction
Midland Reduction
Rosenmund Reduction
Stephen Reduction
Wolff-Kishner Reduction
REARRANGEMENT
Baeyer-Villiger Oxidation
Beckmann Rearrangement
Benzidine Rearrangement
Benzilic Acid Rearrangement
Brook Rearrangement
Curtius Rearrangement (Curtius Reaction)
Demjanov Rearrangement
Di-pi-methane Rearrangement
Favorskii Rearrangement
Fries Rearrangement
Fritsch (-Buttenberg-) Wischell Rearrangement
Hofmann Rearrangement
Lossen Rearrangement
Neber Rearrangement
Pinacol Rearrangement
Pummerer Reaction
Schmidt Reaction (Rearrangement)
Stevens Rearrangement
Wagner-Meerwein Rearrangement
Wolff Rearrangement
Wittig Rearrangement
Aldol Type Reaction (C-C)
Aldol Condensation (General, Directed)
Benzoin Condensation
Claisen Condensation
Claisen Schmidt Condensation
Dieckmann Reaction
Evans Aldol Reaction
Hell-Volhardt-Zelinsky Reaction
Michael Condensation
Mukaiyama Aldol Reaction
Reformatskii Reaction
CONDENSATION (C-C, C=C)
Acyloin Condensation
Benzoin Condensation
Cannizzaro Reaction
Claisen Schmidt Condensation
Darzens Condensation (Darzens-Claisen Reaction)
Dieckmann Reaction
Mannich Reaction
Mitsunobu Reaction
Prins Reaction
Simmons-Smith Reaction
Stobbe Condensation
Thorpe Reactions
CYCLIZATION, CYCLOADDITION
Baldwin's Rules (Ring-Closing Reactions)
Bergman Cyclization
Claisen Rearrangement
Cope Rearrangement
Diels-Alder Reaction
Danishefsky's Diene Cycloaddition
Ene Reaction
Nazarov Cyclization Reaction
Robinson Annelation Reaction
Stork Enamine Reaction
C-C COUPLING
Eglinton Coupling
Grignard Reaction
Heck Reaction
Miyaura Boration Reaction
Negishi Cross Couplig
Sonogashira Coupling
Stille Coupling
Suzuki Coupling
Tsuji-Trost Allyration
Wurtz Reaction
C=C FORMATION
Bamford-Stevans Reaction
Chugaev (Chugaeff) Reaction
Cope Elimination Reaction
Corey-Winter Olefination Reaction
Eschenmoser Fragmentation
Grob Fragmentation
Hofmann Degradation
Horner-Emmons (-Wordsworth) Reaction
Knoevenagel Condensation
McMurry Reaction
Perkin Reaction
Perterson Olefination Reaction
Wittig Reaction
C=O FORMATION
Barton Reaction
Criegee Reaction (Glycol Cleavage)
Meyer (Aldehyde) Synthesis
Nef Reaction
Ritter Reaction
Tiffeneau Reaction (Ring Enlargement)
Vilsmeier Reaction
ESTER, C-O SYNTHESES
Acetoacetic Ester Syntheses
Arndt-Eistert Synthesis
Barbier-Wieland Degradation
Koch-Haff Reaction
Malonic Ester Synthesis
Strecker Amino Acid Synthesis
Prevost Reaction
Williamson Ether Synthesis
BENZENOID
Bamberger Reaction
Friedel Crafts Reaction (Alkylation, Acylation)
Gattermann Aldehyde Synthesis (Formylation)
Gomberg-Bachmann(-Hey) Reaction
Kolbe-Schmitt Reaction
Meerwein Arylation
Meisenheimer Complex
Reimer-Tiemann Reaction
von Richter Reaction
Sandmeyer Reaction
Sommelet (-Hauser) Rearrangement
Ullmann Reaction
HETEROCYCLES
Bischler-Napieralski Reaction.
Fischer Indole Synthesis
Gabriel Synthesis
Hantzsch Pyridine Synthesis
Hofmann-Loffler (Loffler-Freytag) Reaction
Knorr Synthesis
Madelung (Indole) Synthesis
Paal-Knorr Pyrrole Synthesis
Pateruno-Büchi Reaction
Pechmann Condensation
Pictet-Spengler Isoquinoline Synthesis