Results, list

One or more interesting hits can be selected by clicking the small white box next to the structure. The resulting list of literature can be analyzed or refined (Figure 5-14). 

On pages 3 and 4, the calculations for Chapter 5.3 Range Finding Experiments are calculated for the example. The results listed on page 4 in line 38 are listed again in Table 5.3.1 and shown on Figures 5.3.2 and 5.3.3. 

If you have used brainstorming to identify some existing management systems, the resulting list may be lengthy. One way to consider these systems is to subject them to further definition, drawing distinctions such as the following ... 

Auto Search This button initiates from a structure query two or three automated series of search exact and substructure searches in local desktop versions exact, substructure and similarity searches in network version (under ISIS/Host). All the result lists are saved in CHIRBASE using exact-auto , SSS-auto and SIMXX %-auto names. XX is the highest similarity search value (from 80 % to 40 %) allowing to retrieve hits in CHIRBASE. The records in all the lists are unique. The SSS-auto list does not include records that are in the exact-auto list. The SIMXX %-auto list does not include records that are in exact and SSS-auto lists. 

From these preliminary results, we can assume that such enantiophore queries could be used to search in a database of compounds with unknown enantioselectiv-ities. With respect to the percentage of resolved samples that are retrieved in CHIRBASE, the resulting list should contain a similar yield of compounds providing favorable specific interactions with the CSP receptor binding sites. 

The stereochemistry of the carboxylation of 4-substituted ( + )-(/ S)-fra ,v-1-(4-mcthylphcnyl-sulfinylmethyl)cyclohexane after metalation with methyllithium and quenching with carbon dioxide was reported64. The results listed in Table 1 show that the d.r. of around 75 25 under kinetic control changes to 25 75 under thermodynamic control. This is the result of the equilibration of the two diastereomeric metalated species. As shown by the experiment in hexamethylphosphoric Iriamide (IIMI A) (d.r. = 57 43 under kinetic control) an electrophilic assistance of the lithium cation to the electrophilic approach is probably involved. 

The first step was to correlate the annulus data, which, fortunately, are mostly for a pressure of 1000 psia, the same as is the case for rod bundles. A compilation of the 1000 psia data is included in Barnett s report (B6), most of the experimental work being due to Janssen and Kervinen (J3), a summary of the range of system parameters involved in the total of 744 experimental results listed is given below (in all cases, the central rod is uniformly heated, and there is liquid water inlet with vertical upflow) ... 

In the presence of manganese(II) ions the rate of oxidation of H2R by chromic acid decreases . Under favourable experimental conditions (high concentration of alcohol and low concentration of chromate) the diminution of rate is about 50 % which is in accordance with results listed in Table 6, according to which ci = 0.5. The inhibiting effect of manganese(II) on the oxidation of H2R can be explained by reaction (23) followed by step (24). Therefore the induced oxidation of manganese(II) can be described by reactions (26), (23) and (24). 

These steps are summarized in Tables 41.5 and 41.6. The concentration estimates should be compared with the true values 0.1 and 0.2 respectively. For design B the results listed in Table 41.7 are obtained. From both designs a number of interesting conclusions follow. 

The transformation is global. The schemes P and P are strongly computationally equivalent in the restricted sense - if we omit from the test added computational histories of (P,I, a) and (P, I, a) all values of the new variables and all tests involving these variables (i.e. test Z ) for an interpretation I extending I to all of P and P, then the resulting lists are equal. However the loop structure of P has been drastically changed and there is no simple relationship between the graphs of P and P. ... 

Table 33-1 Summary of results obtained from synthetic linearity data using one PCA or PLS factor. We present only those performance results listed by the data analyst as Correlation Coefficient and Standard Error of Estimate...

Common laboratory tests are used to classify the cause of ARF. Functional ARF, which is not included in this table, would have laboratory values similar to those seen in prerenal azotemia. However, the urine osmolality-to-plasma osmolality ratios may not exceed 1.5, depending on the circulating levels of antidiuretic hormone. The laboratory results listed under acute intrinsic renal failure are those seen in acute tubular necrosis, the most common cause of acute intrinsic renal failure. 

Similar calculations were carried out for the remaining ring compounds. The results listed in Table 2 depend somewhat on the particular pair of open-chain reference compounds chosen, but the trends are nevertheless significant. 

The authors (Das, 2005) present the experimental results listed in Table 1, for three different 512 x 512 images. The result is agreeing with our testing well under the assumption that the attacker has accessed the information of image block size. The attack process is presented as follows. We insert a 64 bit watermark considering two cases ... 

The calculation results listed in Table 1.1 are also able to account for the influence of the bridge on the isospecificity. In fact, in agreement with the experimental results,58 the calculated stereoselectivities for a given jt-ligand are generally smaller for the case of the -C(CH3)2- (2-6) than for the -Si(CH3)2- bridge (10-14), while for the case of the -CH2-CH2- bridge the stereoselectivities are often intermediates (compare, e.g., 5, 13, and 23). 

We have examined the rate constants for disproportionation and isomerization for a variety of zeolites, using a commercial-type feed containing 70% m-xylene and 30% o-xylene in a fixed-bed flow reactor. The results, listed in Table I, show the exceptionally low disproportionation/isomerization selectivity of ZSM-5 relative to synthetic faujasite. Synthetic mordenite and ZSM-4 have intermediate selectivities. 

The dehydration of the title alcohols was made over alumina in the presence of piperidine (84). The experimental results listed in Table VII give the primary products. In all experiments the cis-olefins predominate over the trans-. 

After subjecting these starting data to the above described algorithm, and optimizing the values of B and dBjdt, one obtains the results listed in Table III. 

In order to make the calculation, the shift of the parent hydrocarbon must be known or estimated. This process has been applied to a series of compounds with the results listed in Table 8. 

A number of methods have been used for determining Kg values cation selective electrodes, pH-metric methods, conductimetry, calorimetry, temperature-jump relaxation measurements, membrane conductance measurements, nuclear magnetic resonance, optical rotatory dispersion. The results listed in Tables 7—10 have been obtained by various methods and at different ionic strengths so they may not always be strictly comparable. However, the corrections are probably small and the experimental accuracy is generally the same or very similar within a certain ligand type. 

When we use the other predictors to perform all the one-parameter linear correlations, we found the correlation results listed in table 5.6. All these predictors are highly correlated with each other. The parameter with the best theoretical justification... 

Tables 5.1 and 5.2 hst the main physicochemical properties of the modified zeolite characterized by a series of analyzing methods. XRF, XRD, and Al NMR results listed in Table 5.1 showed that with the increasing intensity of CP treatment, nonframework aluminum was ranoved gradually with httle influence on zeohte framework (unit cell size (UCS) changed little), thus the relative crystallinity increased. The removal of nonframework aluminum can also be verified by the FT-IR results shown in Figure 5.1, in which it can be seen that after CP treatment the intensity of the small peak at wave number 3660-3690 cm characterizing nonframework hydroxyl groups decreased step by step.

The N2 adsorption (with BFT and BJH methods) results listed in Table 5.2 showed that the zeolite surface area and pore volume were apparently increased after CP treatment. For example, compared with DASY(0.0) the specific surface area of SOYO-S3 increased by 53 m /g from 618 to 671 m /g, and the pore volume increased from 0.352 to 0.393 mL/g. In addition, DTA analysis data listed in Table 5.2 showed that the thermal stability of the zeolite was further improved. 

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