The Claisen condensation is a carbon–carbon bond forming reaction that occurs between two esters or one ester and another carbonyl compound in the presence... 7 KB (627 words) - 23:49, 14 February 2024 |
In organic chemistry, the Claisen–Schmidt condensation is the reaction between an aldehyde or ketone having an α-hydrogen with an aromatic carbonyl compound... 3 KB (313 words) - 00:27, 23 May 2023 |
as the Claisen condensation and the Dieckman condensation (intramolecular Claisen condensation), which form alcohols as by-products. Condensation reactions... 4 KB (390 words) - 22:54, 4 January 2024 |
which can further react, e.g., the Claisen condensation and its intramolecular equivalent, the Dieckmann condensation. This conversion is exploited in the... 41 KB (4,351 words) - 00:19, 1 May 2024 |
δ-unsaturated carbonyl Claisen condensation, a reaction between esters and carbonyl compounds in the presence of a strong base Ireland–Claisen rearrangement,... 472 bytes (93 words) - 16:34, 11 January 2020 |
elimination Ciamician–Dennstedt rearrangement Claisen condensation Claisen rearrangement Claisen–Schmidt condensation Clemmensen reduction Collins reagent Combes... 38 KB (3,433 words) - 17:07, 5 January 2024 |
Crossed Claisen condensations, in which the enolate and nucleophile are different esters, are also possible. An intramolecular Claisen condensation is called... 25 KB (3,012 words) - 11:17, 17 April 2024 |
inhibiting the reaction. Benzoin condensation Bouveault–Blanc reduction Claisen condensation Dieckmann condensation Bouveault, L.; Locquin, R. (1905)... 8 KB (867 words) - 01:43, 7 May 2024 |
Claisen (German pronunciation: [ˈʁaɪnɐ ˈklaɪzn̩]; 14 January 1851 – 5 January 1930) was a German chemist best known for his work with condensations of... 7 KB (781 words) - 09:43, 7 April 2024 |
Darzens reaction (redirect from Darzens–Claisen reaction) The Darzens reaction (also known as the Darzens condensation or glycidic ester condensation) is the chemical reaction of a ketone or aldehyde with an... 7 KB (717 words) - 13:38, 27 December 2023 |
acceptors. Unlike 1,3-dicarbonyls, which are easily accessed through the Claisen condensation, or 1,5-dicarbonyls, which are commonly made using a Michael reaction... 19 KB (2,357 words) - 19:34, 9 March 2023 |
often performed in organic chemistry classes, and is called Claisen-Schmidt condensation. Prolonged exposure to sunlight initiates [2+2] cycloadditions... 10 KB (741 words) - 10:03, 7 November 2023 |
second carbon from the carboxylic acid. They generally form by the Claisen condensation. The presence of the keto group at the beta position allows them... 6 KB (648 words) - 16:38, 13 August 2023 |
atom. Enols are commonly used in condensation reactions, including the Claisen condensation and the aldol condensation reactions.[citation needed] Examples... 17 KB (2,150 words) - 17:01, 18 April 2024 |
the current AT domain. The ACP-bound elongation group reacts in a Claisen condensation with the KS-bound polyketide chain under CO2 evolution, leaving a... 18 KB (2,158 words) - 10:07, 7 March 2024 |
methoxy group): The key step in the assembly of quinotoxine is a Claisen condensation: 1944: Robert Burns Woodward and W. E. Doering report the synthesis... 18 KB (2,207 words) - 23:38, 11 April 2024 |
remain unknown. Sodium ethoxide is commonly used as a base in the Claisen condensation and malonic ester synthesis. Sodium ethoxide may either deprotonate... 8 KB (695 words) - 18:38, 7 November 2023 |
The fatty acids are synthesized by a series of decarboxylative Claisen condensation reactions from acetyl-CoA and malonyl-CoA. Following each round of... 35 KB (4,020 words) - 10:13, 27 March 2024 |
ethyl acetoacetate is a classic laboratory procedure. It involves Claisen condensation of ethyl acetate. Two moles of ethyl acetate condense to form one... 6 KB (506 words) - 18:45, 4 April 2024 |
diethyl oxalate and 3,3-dimethylpentanoic acid, which reacted by Claisen condensation to yield diketocamphoric acid. Methylation with methyl iodide and... 31 KB (2,898 words) - 00:13, 17 April 2024 |