Applied Organic Chemistry. Surya K. DeЧитать онлайн книгу.
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
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6 Pd‐Catalyzed C
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
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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