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