1. A carbanion is one of several reactive intermediates in organic chemistry. 2. Lysine 289 is thought to stabilize the negatively charged carbanion intermediate. 3. A carbanion are often reactive intermediates in organic chemistry. 4. This effect occurs when the substituents on the carbanion are unsaturated or electronegative. 5. For one, it'd be a carbanion . 6. PLP is employed as it binds to amino groups and stabilises carbanion intermediates. 7. The foundations of carbanion chemistry were laid during Wittig's time in Freiburg. 8. The carbanion then quickly recombines with the electrophile. 9. The newly formed C4 carbanion attacks O2, thus binding it to the substrate. 10. C6 carbanion formation would create dipole interactions with a cationic Lys from the active site.
