An ylide (/ˈɪlaɪd/) or ylid (/ˈɪlɪd/) is a neutral dipolar molecule containing a formally negatively charged atom (usually a carbanion) directly attached...

chemical reaction of an aldehyde or ketone with a triphenyl phosphonium ylide called a Wittig reagent. Wittig reactions are most commonly used to convert...

Nitrile ylides also known as nitrilium ylides or nitrilium methylides, are generally reactive intermediates formally consisting of a carbanion of an alkyl...

Azomethine ylides are nitrogen-based 1,3-dipoles, consisting of an iminium ion next to a carbanion. They are used in 1,3-dipolar cycloaddition reactions...

dipole or a nucleophilic dipole, which includes azomethine ylide, carbonyl ylide, nitrile ylide, azomethine imine, carbonyl imine and diazoalkane. These...

Corey and Michael Chaykovsky. The reaction involves addition of a sulfur ylide to a ketone, aldehyde, imine, or enone to produce the corresponding 3-membered...

15596-07-3) contains the C2O functionality. Sometimes called Bestmann's Ylide, it is a yellow solid. Frenking, Gernot; Tonner, Ralf "Divalent carbon(0)...

charges on adjacent atoms is called an ylide, so sometimes the carbanion form of TPP is referred to as the "ylide form". In several reactions, including...

The Peterson olefination (also called the Peterson reaction) is the chemical reaction of α-silyl carbanions (1 in diagram below) with ketones (or aldehydes)...

analogous to nitrile oxide) Carbonyl imines Some ylides Azomethine ylide Nitrile ylide (RCNCR'2) Carbonyl ylide Thiosulfines (R2CSS) Francis A. Carey, Richard...