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Centre effects

Note that, in situations where a ring fusion produces chiral centres, we can find the number of configurational isomers possible is less than that predicted from the 2" guidelines. This may be the consequence of symmetry, in that an isomer is the same as its mirror image, as we have seen above. However, it can also be the result of restrictions caused by the ring fusion, so that one centre effectively defines the chirality of another, thus reducing the number of combinations. In epoxycyclohexanes, no rran -fused variants can exist. [Pg.112]

Figure 5.3 Displaying individual centre effects and the overall effect... Figure 5.3 Displaying individual centre effects and the overall effect...
Using several different statistical methods, for example, an unpaired t-test, an analysis adjusted for centre effects, ANCOVA adjusting for centre and including baseline risk as a covariate, etc., and choosing that method which produces the smallest p-value is another form of multiplicity and is inappropriate. [Pg.157]

In the next section we will discuss Kaplan-Meier curves, which are used both to display the data and also to enable the calculation of summary statistics. We will then cover the logrank and Gehan-Wilcoxon tests which are simple two group comparisons for censored survival data (akin to the unpaired t-test), and then extend these ideas to incorporate centre effects and also allow the inclusion of baseline covariates. [Pg.194]

Centre effects. None of the study centres should dominate the overall result, neither in terms of number of subjects nor in terms of magnitude of effect... [Pg.242]

Theoretical CDW-EIS models and computer simulations developed during the last decade have been very successful in reproducing experimental data of doubly differential cross sections as a function of ejected electron energy and angle. These studies have enabled us to understand the main characteristics of electron emission spectra and the nature of two centre effects which may be observed in the double differential cross section spectrum. [Pg.311]

CH3 carbon. The results indicate that ligand-centred effects are important and often dominant in controlling the relaxation of ligand nuclei. It is shown that spin density of 10 of an unpaired electron may be significant. This conclusion implies that calculations of geometries of paramagnetic complexes in solution based on T measurements should strictly allow for ligand-centred effects in addition to the metal-centred ones. [Pg.27]

What we must do in order to use both the potential from a given centre and the angular projector on that centre effectively is to ... [Pg.692]

The arguments made in favour of type III approaches are as follows. (I) If treatment effects vary from centre to centre then the only interpretable overall treatment effect would be a straightforward average of the centre effects. (2) (A related point) If we use the treatment estimate as the basis of a test of a hypothesis then the hypothesis we test concerns some average of the true treatment effects in each centre. It would be absurd if this hypothesized average itself depended on the numbers of patients we happened to have recruited to the trial. [Pg.218]

To complete the. off-centre effect, glue Horuontal V" walls (see page 70) across the valley creases. Note that the strap IS flat across the gutter crease. [Pg.82]

Polak, R. (1986). An investigation of the importance of many-centre effects in the diatomics-in-molecules approach. Chemical Physics, 103, 111. [Pg.236]


See other pages where Centre effects is mentioned: [Pg.427]    [Pg.248]    [Pg.322]    [Pg.19]    [Pg.131]    [Pg.15]    [Pg.425]    [Pg.99]    [Pg.222]    [Pg.54]    [Pg.349]    [Pg.441]    [Pg.189]    [Pg.82]   
See also in sourсe #XX -- [ Pg.157 , Pg.194 , Pg.204 , Pg.242 , Pg.248 ]




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Effective quadrupolar centres

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