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List of organic reactions. ... Download as PDF; ... Well-known reactions and reagents in organic chemistry include 0-9. 1,2-Wittig rearrangement; 1,3-Dipolar ...
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).
Organic chemistry is a subdiscipline within chemistry involving the scientific study of the structure, properties, and reactions of organic compounds and organic materials, i.e., matter in its various forms that contain carbon atoms. [1] Study of structure determines their structural formula.
Carbonyl α-substitution reaction; Carboxylation; Carbylamine reaction; Coarctate reaction; Concerted reaction; Conia-ene reaction; Copper-free click chemistry; Cracking (chemistry) Crich beta-mannosylation; Cycloisomerization
Organic Reactions is a peer-reviewed book series that was established in 1942. It publishes detailed descriptions of useful organic reactions.Each article (called a chapter) is an invited review of the primary source material for the given reaction, and is written under tight editorial control, making it a secondary to tertiary‑level source.
The Oxford Chemistry Primers are a series of short texts providing accounts of a range of essential topics in chemistry and chemical engineering written for undergraduate study. The first primer Organic Synthesis: The Roles of Boron and Silicon was published by Oxford University Press in 1991. [ 1 ]
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.
In organic chemistry, the Mannich reaction is a three-component organic reaction that involves the amino alkylation of an acidic proton next to a carbonyl (C=O) functional group by formaldehyde (H−CHO) and a primary or secondary amine (−NH 2) or ammonia (NH 3). [1] The final product is a β-amino-carbonyl compound also known as a Mannich base.