deprotonated
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Acid dissociation constant — Acetic acid, a weak acid, donates a proton (hydrogen ion, high … Wikipedia
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Aldol reaction — The aldol reaction is a powerful means of forming carbon–carbon bonds in organic chemistry.[1][2][3] Discovered independently by … Wikipedia
Isocitrate dehydrogenase — (EC number|1.1.1.42) and (EC number|1.1.1.41), also known as IDH, is an enzyme which participates in the citric acid cycle. It catalyzes the third step of the cycle: the oxidative decarboxylation of isocitrate, producing alpha ketoglutarate (α… … Wikipedia
Metal acetylide — A metal acetylide is an alkyne for which the terminal proton (hydrogen) has been replaced by a metal such as sodium or an organolithium. So, for example, the alkyne CH3C≡CH could be deprotonated to form the acetylide ion CH3C≡C−. Once it has been … Wikipedia
Glycogen phosphorylase — Phosphorylase The crystal structure of the rabit muscle glycogen phosphorylase AMP complex. AMP allosteric site (yellow), phosporylated Ser14 (orange), glycogen binding site (blue), catalytic site (red).[1] … Wikipedia
Nitrile anion — Nitrile anions are nitriles lacking a proton at the position α to the nitrile group. They undergo nucleophilic addition and substitution reactions with various electrophiles.[1] Although nitrile anions are functionally similar to enolates, the… … Wikipedia
Ascorbic acid — This article is about the molecular aspects of ascorbic acid. For information about its role in nutrition, see Vitamin C. L Ascorbic acid … Wikipedia
Phenol — This article is about the molecule. For the class of chemicals containing a phenol group, see Phenols. Phenol … Wikipedia
Pyrrole — Chembox new Name = Pyrrole ImageFile = Pyrrole.png ImageSize = 300px ImageName = Chemical structure of pyrrole IUPACName = Pyrrole Pyrrol Section1 = Chembox Identifiers CASNo = 109 97 7 SMILES = C1=CC=CN1 InChI=1/C4H5N/c1 2 4 5 3 1/h1 5H Section2 … Wikipedia
