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Difference derivative

R = UH3), and morphine (2, R = H), a different derivative of 77 (R = H), ie, (+)-/V-norprotosinomenine (86), serves as the pregenitor of erythraline (87), one of the bases found ia E thnna cristagalli (60). The alkaloids fouad ia all plant parts of E thnna have been iatensively studied because many of them produce smooth muscle paralysis, much like tubocurariae (9). [Pg.545]

The chemistry of benzenecarboxyUc acids generally is the same as that of other carboxyUc acids, which can be converted into esters, salts, acid chlorides, and anhydrides. Each carboxyl group can react separately, so that compounds in which carboxyl groups are converted into different derivatives can be prepared. Because there are aromatic hydrogens available in most of these acids, they also undergo reactions characteristic of the benzene nucleus. Some of the anhydrides have characteristic reactions. [Pg.480]

Cl Disperse Blue 60 is often used as a mixture with slightly different derivatives (116), that is, the methyl group of (40) may be replaced by ethyl (102), propyl (103), or CH2CH2OCH3 (104). [Pg.321]

The coefficient of xV in the three expressions indicates that there exist four different derivatives of cyclopropane of the form (disubstituted cyclopropane with two identical substituents). Two of the four derivatives are mirror images of each other, that is, they form a pair of optical antipodes. If the spatial arrangement is disregarded, only two distinct cyclopropanes with formula are... [Pg.63]

Different derivatives of the benzannulated azonine can also be prepared via the generation of an anion, generated from 8 with methyllithium.14 ... [Pg.572]

The trick is to find the precise way to use and apply the polymer in a particular market sector to add value to a process or to produce cost-effective benefits. Thus, any particular polymer chemistry may be made available to the market in several different derivative forms, in several strengths, and at various prices to suit the particular market conditions. [Pg.166]

Expressions (1) and (2) are called the right difference derivative and the left difference derivative and are denoted by and %, respectively. The difference expressions LjJ" and Ljj" are defined at two points. In other words, these are based on the two-point patterns x, x + h and x — h, X. Moreover, any linear combination of expressions (l)-(2) such as... [Pg.57]

Thus, the right and left difference derivatives generate approximations of order 1 to Lu = u, while the central difference derivative approximates to the second order the same. [Pg.58]

Observe that the right difference derivative at a point x is identical with the left difference derivative at the point x + h, that is, the relation v x) = v (x + h) occurs, permitting us to rewrite (6) as... [Pg.58]

Within these notations, the difference derivative with respect to t becomes... [Pg.63]

Furthermore, we replace the first derivative u (0) by the first difference derivative = (j/j — yo)/h and impose the boundary condition at the point X = 0 such as... [Pg.82]

Since the central difference derivative in t approximates to the second order in r and Au = -f 0 h ), scheme (53) approximates... [Pg.86]

In Section 1 we have already introduced two types of difference derivatives for grid functions the left and the right ones, which correspond to different formulae for difference differentiating of a product... [Pg.98]

The natural replacement of the central difference derivative u x) by the first derivative Uo leads to a scheme of second-order approximation. Such a scheme is monotone only for sufficiently small grid steps. Moreover, the elimination method can be applied only for sufficiently small h under the restriction h r x) < 2k x). If u is approximated by one-sided difference derivatives (the right one for r > 0 and the left one % for r < 0), we obtain a monotone scheme for which the maximum principle is certainly true for any step h, but it is of first-order approximation. This is unacceptable for us. [Pg.184]

It is worth mentioning here that the sign of r x) has had a significant impact on construction of monotone schemes. One way of providing a second-order approximation and taking care of this sign is connected with a monotone scheme with one-sided first difference derivatives for the equation with perturbed coefficients... [Pg.184]

We can calculate the left difference derivative of both sides of this equation with respect to whose use permits us to establish for w(x, ) =... [Pg.205]

In non-metric MDS the analysis takes into account the measurement level of the raw data (nominal, ordinal, interval or ratio scale see Section 2.1.2). This is most relevant for sensory testing where often the scale of scores is not well-defined and the differences derived may not represent Euclidean distances. For this reason one may rank-order the distances and analyze the rank numbers with, for example, the popular method and algorithm for non-metric MDS that is due to Kruskal [7]. Here one defines a non-linear loss function, called STRESS, which is to be minimized ... [Pg.429]

Bis and tris(pyrazolyl)hydroborato ligands are generally prepared as the potassium derivatives by the direct reaction of KBH4 with the appropriate pyrazole (RR pzH), as illustrated in Scheme 1 for the parent system (13). The reaction is extremely general and has been applied to a number of different derivatives, which have included the incorporation of chiral (14, 15) and tethered (16) substituents. However, if the alkyl substituents of the pyrazole are inequivalent (i.e., R + R ), a potential problem may be encountered with the formation of isomeric products, in which either of the R and R substituents may occupy the 3-position of the poly(pyrazolyl)borato ligand. Nevertheless, if the difference in steric demands of R and R is large, there is a strong... [Pg.297]

The dithioformato complex OsH(k2-S2CH)(CO)(P Pr3)2 reacts with HBF4-OEt2 to give two different derivatives depending upon the nature of the solvent used (Scheme 25). The addition of one equiv. of HBF4-OEt2 to a solution of the... [Pg.28]

Electrochemical studies indicate that the redox behaviours of the different derivatives are dominated by the nature of the chalcogen at position 2, with the selenium containing cations more readily reduced (by more than 0.1 V) than the sulfur analogues.82 The difference has been ascribed to the extent of delocalisation of the positive charge away from the heterocycle, onto the fused aromatic ring. [Pg.754]

A comparison with its different derivatives shows that 4 -OH is not a sole reactive group responsible for the antioxidant activity of resveratrol, while the trans-conformation is absolutely necessary for the inhibition of cell proliferation [187], However, similar to flavonoids resveratrol may exhibit prooxidant properties, for example to promote DNA fragmentation, although its prooxidant activity seems to be unimportant under physiological conditions [188],... [Pg.872]


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