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Hofmann Isonitrile synthesis, Carbylamine reaction; Hofmann product; Hofmann rearrangement; Hofmann–Löffler reaction, Löffler–Freytag reaction, Hofmann–Löffler–Freytag reaction; Hofmann–Martius rearrangement; Hofmann's rule; Hofmann–Sand reaction; Homo rearrangement of steroids; Hooker reaction; Horner–Wadsworth–Emmons ...
Books have been published devoted exclusively to name reactions; [2] [3] [4] the Merck Index, a chemical encyclopedia, also includes an appendix on name reactions. As organic chemistry developed during the 20th century, chemists started associating synthetically useful reactions with the names of their discoverers or developers.
Organic chemistry has a strong tradition of naming a specific reaction to its inventor or inventors and a long list of so-called named reactions exists, conservatively estimated at 1000. A very old named reaction is the Claisen rearrangement (1912) and a recent named reaction is the Bingel reaction (1993).
Download as PDF; Printable version; ... This category encompasses the organic reaction archetype, and includes organic name reactions. See also ... (chemistry) Crich ...
The IUPAC Nomenclature for Organic Chemical Transformations is a methodology for naming a chemical reaction.. Traditionally, most chemical reactions, especially in organic chemistry, are named after their inventors, the so-called name reactions, such as Knoevenagel condensation, Wittig reaction, Claisen–Schmidt condensation, Schotten–Baumann reaction, and Diels–Alder reaction.
Abramov reaction; Achmatowicz reaction; Adams decarboxylation; Adkins–Peterson reaction; Akabori amino-acid reaction; Albright–Goldman oxidation; Alder ene reaction; Aldol–Tishchenko reaction; Algar–Flynn–Oyamada reaction; Allan–Robinson reaction; Allen–Millar–Trippett rearrangement; Amadori rearrangement; Andrussow process ...
is an alkaline solution of potassium permanganate; used in organic chemistry as a qualitative test for the presence of unsaturation, such as double bonds; N-Bromosuccinimide: used in radical substitution and electrophilic addition reactions in organic chemistry. Also acts as a mild oxidizer to oxidize benzylic or allylic alcohols.
The Julia olefination (also known as the Julia–Lythgoe olefination) is the chemical reaction used in organic chemistry of phenyl sulfones (1) with aldehydes (or ketones) to give alkenes (olefins)(3) after alcohol functionalization and reductive elimination using sodium amalgam or SmI 2. The reaction is named after the French chemist Marc Julia.