Correlation steric

The careful and extensive stereochemical investigations of the tropane bases rendered a reconsideration of their pharmacological effects possible in correlating steric structure with physiological activity in a more precise mtmner than heretofore. 

There are now a few hundred practical applications of CoMFA in drug design. Most applications are in the field of ligand-protein interactions, describing affinity or inhibition constants. In addition, CoMFA has been used to correlate steric and electronic parameters.Less appropriate seems the application of CoMFA to in vivo data, even if lipophilicity is considered as an additional parameter. As most CoMFA applications in drug design have been comprehensively reviewed in three books and in some reviews, " Table 1 gives only an overview of some typical applications that have been reported in the last few years. 

Hydroformylation reactions can be carried out with a variety of precatalysts and also with or without a spectator ligand such as PPhj. The choice of ligand has a significant influence on the regioselectivity of a hydroformylation reaction. Many studies have been made to correlate steric, electronic, and other structural properties of both monodentate and bidentate phosphines with their overall catalytic performances. 

The solubility of a compound is thus affected by many factors the state of the solute, the relative aromatic and aliphatic degree of the molecules, the size and shape of the molecules, the polarity of the molecule, steric effects, and the ability of some groups to participate in hydrogen bonding. In order to predict solubility accurately, all these factors correlated with solubility should be represented numerically by descriptors derived from the structure of the molecule or from experimental observations. 

The value of d obtained by linear regression is 0.96 with a correlation coefficient of 0.9985. For 2 alkylpyridines 8 is 2.030 (256), which leads to the conclusion that 2-alkylpyridines are twice as sensitive to steric effects as their thiazole analogs. 

Quantitative Structure—Activity Relationships. Many quantitative stmcture—activity relationship (QSAR) studies of progestins have appeared in the Hterature and an extensive review of this work is available (174). QSAR studies attempt to correlate electronic, steric, and/or hydrophobic properties to progestational activity or receptor binding affinity. A review focusing on the problems associated with QSAR of steroids has been pubUshed (175). 

The alkyl and alkoxy substituents of phosphate or phosphonate esters also affect the phosphorylating abiUty of the compound through steric and inductive effects. A satisfactory correlation has been developed between the quantitative measure of these effects, Tafts s O, and anticholinesterase activity as well as toxicity (33). Thus long-chain and highly branched alkyl and alkoxy groups attached to phosphoms promote high stabiUty and low biological activity. 

Satisfactory Brpnsted correlations for a-substituted azoles offer further evidence of the lesser importance of steric effects in the azole series (78AHC(22)7l). 

An example of the application of molecular mechanics in the investigation of chemical reactions is a study of the correlation between steric strain in a molecule and the ease of rupture of carbon-carbon bonds. For a series of hexasubstituted ethanes, it was found that there is a good correlation between the strain calculated by the molecular mechanics method and the rate of thermolysis. Some of the data are shown in Table 3.3. 

Finally, we assume that the fields 4>, p, and u vary slowly on the length scale of the lattice constant (the size of the molecules) and introduce continuous approximation for the thermodynamical-potential density. In the lattice model the only interactions between the amphiphiles are the steric repulsions provided by the lattice structure. The lattice structure does not allow for changes of the orientation of surfactant for distances smaller than the lattice constant. To assure similar property within the mesoscopic description, we add to the grand-thermodynamical potential a term propor-tional to (V u) - -(V x u) [15], so that the correlation length for the orientational order is equal to the size of the molecules. 

The ortho effect may consist of several components. The normal electronic effect may receive contributions from inductive and resonance factors, just as with tneta and para substituents. There may also be a proximity or field electronic effect that operates directly between the substituent and the reaction site. In addition there may exist a true steric effect, as a result of the space-filling nature of the substituent (itself ultimately an electronic effect). Finally it is possible that non-covalent interactions, such as hydrogen bonding or charge transfer, may take place. The role of the solvent in both the initial state and the transition state may be different in the presence of ortho substitution. Many attempts have been made to separate these several effects. For example. Farthing and Nam defined an ortho substituent constant in the usual way by = log (K/K ) for the ionization of benzoic acids, postulating that includes both electronic and steric components. They assumed that the electronic portion of the ortho effect is identical to the para effect, writing CTe = o-p, and that the steric component is equal to the difference between the total effect and the electronic effect, or cts = cr — cte- They then used a multiple LFER to correlate data for orrAo-substituted reactants. 

Because 5 is not well correlated with Ei, these two steric constants contain different information. Berg et al. conclude that S is a measure of the pure steric effect. 

Correlations with o in carboxylic acid derivative reactions have been most successful for variations in the acyl portion, R in RCOX. Variation in the alkyl portion of esters, R in RCOOR, has not led to many good correlations, although use of relative rates of alkaline and acidic reactions, as in the defining relation, can generate linear correlations. The failure to achieve satisfactory correlations with cr for such substrates may be a consequence of the different steric effects of substituents in the acyl and alkyl locations. It has been shown that solvolysis rates of some acetates are related to the pA", of the leaving group, that is, of the parent alcohol. The pK of alcohols has been correlated with but this relationship... 

Some authors use O] instead of cr as the substituent constant in such correlations.) An example is provided by the aminolysis of phenyl esters in dioxane the substrates RCOOPh were reacted with -butylamine, and the observed first-order rate constants were related to amine concentration by = k2 [amine] kj [amine]. The rate constants kz and k could be correlated by means of Eq. (7-54), the reaction constants being p = +2.14, b = + 1.03 (for A 2) and p = -1-3.03,8 = -1-1.08 (for ks). Thus, the two reactions are about equally sensitive to steric effects, whereas the amine-catalyzed reaction is more susceptible to electronic effects than is the uncatalyzed reaction. 

The quasi racemate method proved very useful for the steric correlation of these compounds with the corresponding benzene deriva-... 

The good correlation found between the reactivities of 2-chloro-3-cyano-5-nitropyridine and the polar effects of the substituents on the aniline reagent has enabled Chapman and his co-workers to illustrate the steric requirements of the reagent by including in their studies... 

---