Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Carbonyl compounds, anionic cyclisation

The first cyclisations to be put to synthetic use were those of aryl lithiums onto carbonyl compounds, imines and epoxides. These are known as Parham cyclisations , and the method for transforming an aryl bromide to an aryllithium the Parham protocol , after W. E. Parham, who developed the reaction. We will survey the use of Parham cyclisations in synthesis, before assessing intramolecular attack of other electrophiles. The most important of these are the alkenes, and the usefulness of anionic cyclisations onto unactivated double bonds compares very favourably with radical cyclisations, particularly with regard to stereochemical control. [Pg.282]

Anionic cyclisations onto carbonyl compounds and derivatives... [Pg.282]

Michael addition of phthalide anions with a,P-unsaturated carbonyl compounds, followed by cyclisation provide substituted naphthols. [Pg.81]


See other pages where Carbonyl compounds, anionic cyclisation is mentioned: [Pg.282]    [Pg.70]    [Pg.47]    [Pg.33]    [Pg.160]    [Pg.302]    [Pg.213]    [Pg.282]    [Pg.302]   


SEARCH



Anionic carbonyls

Anionic cyclisation

Carbonyl anions

Carbonylate anions

Compounds anionic

© 2024 chempedia.info