Applied Organic Chemistry. Surya K. De

target="_blank" rel="nofollow" href="#ulink_321e7d05-8bfd-5679-a6cb-f12312aeece0">Houben–Hoesch Reaction Kolbe–Schmitt Reaction Reimer–Tiemann Reaction Vilsmeier–Haack Reaction References Bogert–Cook Reaction or Synthesis of Phenanthrene Friedel–Crafts Reaction Gattermann Aldehyde Synthesis Gattermann–Koch Aldehyde Synthesis Haworth Reaction Houben–Hoesch Reaction Kolbe–Schmitt Reaction Reimer–Tiemann Reaction Vilsmeier–Haack Reaction

      14  6 Pd‐Catalyzed CC Bond‐Forming Reactions Suzuki Coupling Reaction Heck Coupling Reaction (Mizoroki–Heck Reaction) Negishi Coupling Reaction Stille Coupling Reaction (Migita–Kosugi–Stille Coupling Reaction) Sonogashira Coupling Reaction Kumada Cross‐Coupling Hiyama Coupling Reaction Liebeskind–Srogl Coupling Reaction Fukuyama Coupling Reaction Buchwald–Hartwig Coupling Reaction (Buchwald–Hartwig Amination) Tsuji–Trost Allylation References Heck Coupling Reaction (Mizoroki–Heck Reaction) Negishi Coupling Reaction Stille Coupling Reaction (Migita–Kosugi–Stille Coupling Reaction) Sonogashira Coupling Reaction Kumada Cross‐Coupling Hiyama Coupling Reaction Liebeskind–Srogl Coupling Reaction Fukuyama Coupling Reaction Buchwald–Hartwig Coupling Reaction (Buchwald–Hartwig Amination) Tsuji–Trost Allylation

      15  7 Multicomponent Reaction Biginelli Reaction (3‐Component Reaction [3‐CR]) Gewald Reaction (3‐Component Reaction [3‐CR]) Hantzsch Pyridine Synthesis Mannich Reaction Passerini Reaction (3‐Component Reaction [3‐CR]) Strecker Amino Acid Synthesis Ugi Reaction (4‐Component Reaction [4‐CR]) Asinger Reaction (4‐Component Reaction [A‐4CR]) References Gewald Reaction Hantzsch Pyridine Synthesis Mannich Reaction Passerini Reaction Strecker Amino Acid Synthesis Ugi Reaction Asinger Reaction

      16  8 Oxidations and Reductions Oxidation Reactions Dess–Martin Oxidation Jones Oxidation Swern Oxidation Pfitzner–Moffatt Oxidation Tamao–Fleming Oxidation Tamao–Kumada Oxidation Oppenauer Oxidation Riley Oxidation Ley–Griffith Oxidation Criegee Oxidation (Criegee Glycol Cleavage) Criegee Ozonolysis Reduction Reactions Bouveault–Blanc Reduction Clemmensen Reduction Corey–Bakshi–Shibata Reduction (also known as Itsuno–Corey reduction) Noyori Asymmetric Hydrogenation Luche Reduction Meerwein–Ponndorf–Verley Reduction Mozingo Reduction Rosenmund

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