Amino group, inductive effect

The basic piSTa values, which have to be considered as equilibrium values, including those of anhydrous and hydrated species, reveal a destabilizing inductive effect of the 6- and 7-methyl group towards 3,4-hydrate formation, as do also the 2-methylamino and 2-dimethylamino groups for additional steric reasons. If the cation of 2-aminopteridine did not add water its value would be about 1.6, arrived at by substracting from the piSTa 2.6 of the essentially anhydrous 2-amino-4,7-dimethylpteridine cation 0.3 for the 7- and 0.7 for the 4-methyl group. The difference between the observed value of 4.29 and the... 

The assumed transition state for this reaction is shown in Scheme 5.5. The two bulky t-butoxy groups are expected to locate at the two apical positions. One of the 3,3 -phenyl groups would effectively shield one face of an imine, and consequently, a diene attacks from the opposite side. Judging from this model, similar selectivities were expected in the Mannich-type reactions of imines with silyl eno-lates. Actually, when ligand 10 was used in the reaction of imine la with S-ethyl-thio-l-trimethylsiloxyethene, the corresponding / -amino thioester was obtained in 84% ee (Scheme 5.6). As expected, the sense of the chiral induction in this case was the reverse of that observed when using catalyst 6 [12, 25]. 

A group with a more powerful (electron-withdrawing) inductive effect, e.g. NOa, is found to have rather more influence. Electron-withdrawal is intensified when the nitro group is in the o- or p-position, for the interaction of the unshared pair of the amino nitrogen with the delocalised it orbital system of the benzene nucleus is then enhanced. The neutral molecule is thus stabilised even further with respect to the cation, resulting in further weakening as a base. Thus the nitro-anilines are found to have related p a values ... 

B. Inductive Effect of the Amino Group and Related Groups. 517... 

Deprotonation provides the necessary electron push to kick out the electron pair joining C(6) with the nitrobenzene oxygen. If, however, N(l) is alkylated (as with the nucleosides and nucleotides), OH catalysis is much less efficient since it now proceeds by deprotonation from N(3) (with the uracils) or from the amino group at C(4) (with the cytosines). In these cases the area of deprotonation is separated from the reaction site by a (hydroxy)methylene group which means that the increase in electron density that results from deprotonation at N(3) is transferable to the reaction site only through the carbon skeleton (inductive effect), which is of course inefficient as compared to the electron-pair donation from N(l) (mesomeric effect) [26]. Reaction 15 is a 1 1 model for the catalytic effect of OH on the heterolysis of peroxyl radicals from pyrimidine-6-yl radicals (see Sect. 2.4). 

We can appreciate that ionization of the carboxylie acid is affected by the electron-withdrawing inductive effect of the ammonium residue hence the increased acidity when compared with an alkanoic acid. Similarly, loss of a proton from the ammonium cation of the zwitterion is influenced by the electron-donating inductive effect from the carboxylate anion, which should make the amino group more basic than a typical amine. That this is not the case is thought to be a solvation effect (compare simple amines). 

Groups that are particularly strong electron releasers do not achieve this by an inductive effect, but they have heteroatoms with lone pair electrons that are able to stabilize resonance structures by transferring the charge to the heteroatom, i.e. an electron-releasing resonance effect. An amino group is typical of this type of substituent. 

It can be seen that lone pair donation creates another favourable resonance form only when electrophilic attack is ortho or para to the amino group. There is a small electron-withdrawing inductive effect... 

The imidazole side-chain of histidine has a value of 6.0, making it a weaker base than the unsubstituted imidazole. This reflects the electron-withdrawing inductive effect of the amino group, or, more correctly the ammonium ion, since amino acids at pH values around neutrality exist as doubly charged zwitterionic forms (see Box 4.7). Using the Henderson-Hasselbalch equation, this translates to approximately 9% ionization of the heterocyclic side-chain of histidine at pH 7 (see Box 4.7). In proteins, plCa values for histidine side-chains are estimated to be in range 6-7, so that the level of ionization will, therefore, be somewhere between 9 and 50%, depending upon the protein. 

The rates depend on the thiol structure, and correlate well with inductive effects. Thus, the -NH2 and COO groups destabilize and stabilize the red adduct, respectively. When the groups are blocked by acetylation or esterification, their influence is suppressed, as shown by IV-acetylcysteine, which forms the most stable adduct in the series because of the unprotected COO and the acetylated amino group. 

In diamines such as 4,4 -diaminodiphenylmethane, 4,4 -diaminodiphenyl sulphone or 1,6-hexamethylenediamine, the substitution effect is practically absent641 although this may not be the case for di- and polyamines where the distance between the amino groups is not large allowing inductive and steric effects to be operative 59,68 ... 

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