Publication

Three-Component Povarov Reaction–Heteroannulation with Arynes: Synthesis of 5,6-Dihydroindolo[1,2‑a]quinolines

Qian Wang, Jieping Zhu, Ala Bunescu
2014
Journal Articles

Résumé

A reaction of 2-acyl substituted tetrahydroquinolines, prepared by Lewis acid-catalyzed three-component reaction of α-oxo aldehydes, anilines, and dienophiles, with in situ generated arynes afforded 5,6-dihydroindolo[1,2-a]- quinolines in good to excellent yields.

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https://infoscience.epfl.ch/entities/publication/814d2d48-8255-4d29-964f-ed68fdedfed1

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Qian Wang, Jieping Zhu, Ala Bunescu
2014
Journal Articles

Résumé

Source officielle

https://infoscience.epfl.ch/entities/publication/814d2d48-8255-4d29-964f-ed68fdedfed1

À propos de ce résultat

Concepts associés (16)

Aldéhyde

alt=Structure atomique de l'aldéhyde.|vignette|Structure atomique de l'aldéhyde. Un aldéhyde est un composé organique, faisant partie de la famille des composés carbonylés, dont l'un des atomes de carbone primaire (relié au plus à 1 atome de carbone) de la chaîne carbonée porte un groupement carbonyle. Un aldéhyde contient donc la séquence : L'aldéhyde le plus simple (R réduit au seul atome H) est le formaldéhyde (ou méthanal), aussi appelé formol lorsqu'il est en solution aqueuse : 75px Un aldéhyde dérive formellement d'un alcool primaire (oxydation) dont le groupement hydroxyde -OH est en bout de chaîne et se forme à la suite de l'enlèvement de deux atomes H d'où le nom « alcool déshydrogéné » ou aldéhyde.

Alkyne trimerisation

An alkyne trimerisation is a [2+2+2] cycloaddition reaction in which three alkyne units () react to form a benzene ring. The reaction requires a metal catalyst. The process is of historic interest as well as being applicable to organic synthesis. Being a cycloaddition reaction, it has high atom economy. Many variations have been developed, including cyclisation of mixtures of alkynes and alkenes as well as alkynes and nitriles. Trimerisation of acetylene to benzene is highly exergonic, proceeding with a free energy change of 142 kcal/mol at room temperature.

Ene reaction

In organic chemistry, the ene reaction (also known as the Alder-ene reaction by its discoverer Kurt Alder in 1943) is a chemical reaction between an alkene with an allylic hydrogen (the ene) and a compound containing a multiple bond (the enophile), in order to form a new σ-bond with migration of the ene double bond and 1,5 hydrogen shift. The product is a substituted alkene with the double bond shifted to the allylic position. This transformation is a group transfer pericyclic reaction, and therefore, usually requires highly activated substrates and/or high temperatures.

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