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Convex addition

Convex additive terms remain unmodified in these functions. [Pg.66]

Exercise. For a certain system let px and p2 be two different density matrices (describing two different ensembles). Convex addition of them (involving two positive numbers /L1 A2) is defined by... [Pg.425]

Unique chemistry is associated with the cyclopentenone all five carbon atoms can be functionalized, and the endo-methyl groups of the acetonide assure clean stereoselective addition of the alkenylcopper reagent from the convex side. The use of the acetonide group to control enolate regioselectivity and to mask alcohols should be generally applicable. [Pg.277]

The relationship between 20 and reserpine (1) is close like reserpine, intermediate 20 possesses the linear chain of all five rings and all six stereocenters. With the exception of the 3,4,5-tri-methoxybenzoate grouping, 20 differs from reserpine (1) in one very important respect the orientation of the ring C methine hydrogen at C-3 in 20 with respect to the molecular plane is opposite to that found in reserpine. Intermediate 20 is a reserpate stereoisomer, epimeric at position 3, and its identity was secured by comparison of its infrared spectrum with that of a sample of (-)-methyl-O-acetyl-isoreserpate, a derivative of reserpine itself.9 Intermediate 20 is produced by the addition of hydride to the more accessible convex face of 19, and it rests comfortably in a conformation that allows all of the large groups attached to the D/E ring skeleton to be equatorially disposed. [Pg.61]

Because it is concave and elliptical, the secondary mirror of a Gregorian telescope allows for simpler fabrication test set-ups, as a point-like source placed at one of the foci of the ellipse should be re-imaged aberration-free at the other focus. Convex hyperbolic mirrors require more complex set-ups. This disadvantage is usually more than balanced by the more compact arrangement, the savings implied by the shorter telescope structure and more compact enclosure offsetting the additional cost and complexity of the secondary mirror test set-up. This trade-off, however, applies in the context of current technology-... [Pg.27]

The lower symmetry of nanorods (in comparison to nanoshells) allows additional flexibility in terms of the tunability of their optical extinction properties. Not only can the properties be tuned by control of aspect ratio (Figure 7.4a) but there is also an effect of particle volume (Figure 7.4b), end cap profile (Figure 7.4c), convexity of waist (Figure 7.4d), convexity of ends (Figure 7.4e) and loss of rotational symmetry (Figure 7.4f). [Pg.327]

Some examples of conjugate addition reactions of allylic silanes are given in Scheme 9.5. Entries 1 to 3 illustrate the synthesis of several (3-allyl ketones. Note that Entry 2 involves the creation of a quaternary carbon. Entry 4 was used in the synthesis of a terpenoid ketone, (+)-nootkatone. Entry 5 illustrates fluoride-mediated addition using tetrabutylammonium fluoride. These conditions were found to be especially effective for unsaturated esters. In Entry 6, the addition is from the convex face of the ring system. Entry 7 illustrates a ring closure by intramolecular conjugate addition. [Pg.833]

The addition of inequality constraints complicates the optimization. These inequality constraints can form convex or nonconvex regions. If the region is nonconvex, then this means that the search can be attracted to a local optimum, even if the objective function is convex in the case of a minimization problem or concave in the case of a maximization problem. In the case that a set of inequality constraints is linear, the resulting region is always convex. [Pg.54]

Strictly speaking, additionally the particles must be convex (i.e., without indentations or holes) and homogeneous (i.e., without density oscillations)... [Pg.111]

For simplicity, consider the problem Min f(x) subject to g(x) < 0 where each function can be defined by additive terms. Convex relaxations for/(x) and g(x) can be derived in the following ways ... [Pg.66]

Schreiber and his coworkers have published extensively over the past decade on the use of this photocycloaddition for the synthesis of complex molecules730 81. Schreiber was the first to recognize that the bicyclic adducts formed in these reactions could be unmasked under acidic conditions to afford threo aldol products of 1,4-dicarbonyl compounds (175 to 176) (Scheme 40). The c -bicyclic system also offers excellent stereocontrol in the addition of various electrophilic reagents (E—X) to the enol ether of these photoadducts on its convex face (175 to 177). This strategy has been exploited in the synthesis of a variety of architecturally novel natural products. [Pg.299]

Figure 2 shows FFEM images of Mal3 (Phyt)2/SQDG (9 1 mol/mol) vesicle membranes in the presence (Fig. 2A, B) or in the absence (Fig. 2C, D) of BR. Small particles were observed in Figure 2A, B, whereas no such particles were observed for pure Mai (Phyt)2/SQDG vesicles. In addition, two fracture faces of the bilayer membranes, a convex surface (a hydrophobic face of an inner leaflet, Fig. 2A) and a concave surface (a hydrophobic face of an outer leaflet, Fig. 2B) exhibited intramembraneous particles, suggesting BR was incorporated into vesicles transmembraneously. Figure 2 shows FFEM images of Mal3 (Phyt)2/SQDG (9 1 mol/mol) vesicle membranes in the presence (Fig. 2A, B) or in the absence (Fig. 2C, D) of BR. Small particles were observed in Figure 2A, B, whereas no such particles were observed for pure Mai (Phyt)2/SQDG vesicles. In addition, two fracture faces of the bilayer membranes, a convex surface (a hydrophobic face of an inner leaflet, Fig. 2A) and a concave surface (a hydrophobic face of an outer leaflet, Fig. 2B) exhibited intramembraneous particles, suggesting BR was incorporated into vesicles transmembraneously.
Although convexity is desirable, many real-world problems turn out to be non-convex. In addition, there is no simple way to demonstrate that a nonlinear problem is a convex problem for all feasible points. Why, then is convex programming studied The main reasons are... [Pg.126]

In most cases a clear maximum gap is revealed (here the gap between the second and the third bar). The atomic environment is then constructed with the atoms to the left of this gap (8 + 6 in the example of CsCl). To avoid in particular cases bad or ambiguous descriptions, however, a few additional rules have been considered. When for instance two (or more) nearly equal maximum gaps were observed, a selection was made in order to keep, in a given structure type, the number of different AET as small as possible. A convexity criterion for the environment polyhedron was also considered. The coordination polyhedron has to be defined as the maximum convex volume around only one central atom enclosed by convex faces with all coordinating faces lying at the intersections of at least three faces. This rule was especially used where no clear maximum gap was detectable. [Pg.132]

As stated, the Archimedean solids constitute a family of 13 convex uniform polyhe-dra made up of two or more regular polygons and, like the Platonic solids, possess either 32, 432, or 532 symmetry. As a result, the three coordinate directions within each solid are equivalent, making these polyhedra, in addition to the Platonic solids, models for spheroid design. [Pg.143]

B, inhibitory Draw an upwardly convex curve labelled B which begins and terminates at the same points as line A. This represents inhibition because now, at any given dose of drug A, more of drug B needs to be given to maintain a constant effect compared with an additive relationship. [Pg.88]

C, synergistic Finally draw a downwardly convex curve labelled C. This represents synergy in that less of drug B is required at any point compared with what would be seen with an additive relationship. [Pg.88]


See other pages where Convex addition is mentioned: [Pg.64]    [Pg.64]    [Pg.351]    [Pg.28]    [Pg.200]    [Pg.22]    [Pg.38]    [Pg.59]    [Pg.321]    [Pg.321]    [Pg.337]    [Pg.388]    [Pg.110]    [Pg.115]    [Pg.101]    [Pg.158]    [Pg.109]    [Pg.821]    [Pg.548]    [Pg.522]    [Pg.599]    [Pg.66]    [Pg.68]    [Pg.69]    [Pg.69]    [Pg.137]    [Pg.204]    [Pg.135]    [Pg.74]    [Pg.389]    [Pg.986]    [Pg.138]   
See also in sourсe #XX -- [ Pg.64 , Pg.425 ]




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