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Transformation function

Tran orm-based or long-range strategies The retrosynthetic analysis is directed toward the application of powerful synthesis transforms. Functional groups are introduced into the target compound in order to establish the retion of a certain goal transform (e.g., the transform for the Diels-Alder reaction, Robinson annulation, Birch reduction, halolactonization, etc.). [Pg.575]

The most general method i.s a form of parametric mapping in which the transformation functions, and in Equation (2.26), are polynomials... [Pg.35]

Isoparametric transformation functions between a global coordinate system and local coordinates are, in general, written as... [Pg.35]

In order to establish an isoparametric mapping between the master element shown in Figure 2.23 and the elements in the global domain (Figure 2.20) we use the elemental shape funetions to formulate a transformation function as... [Pg.52]

Actuate. To make possible or enable transform function on a target in a manner analogous to that in which a structural subunit can activate a molecule for chemical reaction. The verb actuate is the retrosynthetic equivalent of activate in the synthetic direction. [Pg.96]

We are effectively transforming functional identity into topological information i.e. different choices of rules correspond to different topologies and all rules are taken to be simple functions of local sums. [Pg.261]

These theorems give explicit forms to the transformation functions relating configuration space to occupation number space. [Pg.453]

The basic component of the neural network is the neuron, a simple mathematical processing unit that takes one or more inputs and produces an output. For each neuron, every input has an associated weight that defines its relative importance, and the neuron simply computes the weighted sum of all the outputs and calculates an output. This is then modified by means of a transformation function (sometimes called a transfer or activation function) before being forwarded to another neuron. This simple processing unit is known as a perceptron, a feed-forward system in which the transfer of data is in the forward direction, from inputs to outputs, only. [Pg.688]

The weighting functions used to improve line shapes for such absolute-value-mode spectra are sine-bell, sine bell squared, phase-shifted sine-bell, phase-shifted sine-bell squared, and a Lorentz-Gauss transformation function. The effects of various window functions on COSY data (absolute-value mode) are presented in Fig. 3.10. One advantage of multiplying the time domain S(f ) or S(tf) by such functions is to enhance the intensities of the cross-peaks relative to the noncorrelation peaks lying on the diagonal. [Pg.168]

Dynamic models expressed in terms of transform functions can be solved by digital simulation by transposing the transfer function into an equivalent set of differential equations, as shown by Ord-Smith and Stephenson (1975) and by Matko et al. (1992). Also some languages include special transfer function subroutines. [Pg.86]

This is based on the example of Matko, Korba and Zupancic (1), who describe methods of simulating process transform functions, based on partitioned and nested forms of solution. Here the process transfer function is given by... [Pg.524]

The third alternative to generate the diagonalized form is to use the state space to state space transformation function. The transformation is based on the modal matrix that we obtained earlier. [Pg.236]

Fig. 5. The / ,-< < iirection (i.e. the density-to-flux transformation) function for the current experimental setup. Fig. 5. The / ,-< < iirection (i.e. the density-to-flux transformation) function for the current experimental setup.
The integral breadth of a ID, even and Fourier-transformable function h (r) is defined by... [Pg.42]

Then it follows from the slice theorem Eq. (2.38) for the integral breadth of the Fourier transformed function H (5)... [Pg.42]

There are also forms of nonlinear PCR and PLS where the linear PCR or PLS factors are subjected to a nonlinear transformation during singular value decomposition the nonlinear transformation function can be varied with the nonlinearity expected within the data. These forms of PCR/PLS utilize a polynomial inner relation as spline fit functions or neural networks. References for these methods are found in [7], A mathematical description of the nonlinear decomposition steps in PLS is found in [8],... [Pg.165]

The localized molecular orbitals (LMOs) can be defined as the unitary transformation of CMOs that (roughly speaking) makes the transformed functions as much like the localized NBOs as possible,24... [Pg.115]

Modify the form of the transform function, convert this into differential equation format and study the resulting response characteristics. [Pg.436]

One of the reasons for using these transformation functions is the ease of evaluating the derivatives that is required for minimization of the error function. [Pg.252]

The neural network model for the two binary systems viz. tert-butanol+2-ethyl-l-hexanol and n-butanol+2-ethyl-l-hexanol is based on the experimental data reported by Ghanadzadeh et al. [23], The summary of the data is shown in tables 1 and 2. All neural networks take numeric input and produce numeric output. The transformation function of a neuron is typically chosen so that it can accept input in any range, and produce output in a strictly limited range. Although the input can be in any range, there is a saturation effect so that the unit is only sensitive to inputs within a fairly limited range. Numeric values have to be scaled into a range that is appropriate for the network. [Pg.252]

This problem was solved approximately in 1947 (B2, K9, Jl), wherein it was suggested that the transformed function of y be expanded in a linear Taylor series to provide... [Pg.114]

Defining in this way permits us to use transfer functions in the z domain [Eq. (18.57)] just as we use transfer functions in the Laplace domain. G,, is the z transform of the impulse-sampled response of the process to a unit impulse function <5( . In z-transforming functions, we used the notation =... [Pg.638]

At any rate the practitioner must follow a two-step process in setting up a calibration graph 1. Stabilize the response variance across the range needed and 2. choose an appropriate calculation function model. The response data is stabilized currently in two ways, either by weighting on a level-by-level basis or by applying some transformation function in the same manner to all the response values. The model chosen must approximate the data. It can be that a simple linear (as shown by a statistical test) function can serve this purpose adequately. The use of Mitchell s multiple linear function has been successfully... [Pg.185]

Clearly, the quantity = Xj/j) maps the region 0 < S < < into the interval 0 < S 2. The value of % = 2 is the maximum value of the Hill coefficient for the case m-l. One should be careful, however, to note that these particular methods are valid only for the case of two sites. When m > 2 there are various types of cooperativities and, in general, there is no single parameter that describes the cooperativity in the system. Even for the case m = 2 one could be misled in estimating the cooperativity of the system if one were to rely only on the/orm or the shape of the BI or any of its transformed functions, as will be demonstrated in Section 4.6 and again in Section 4.8 and Appendix F. [Pg.77]

To conclude, we emphasize that the form or the shape of the BI (or any of its transformed functions) is a manifestation of the type of cooperativity in the system. In the particular case (m = 2) discussed in this section, either Eq. (4.3.9) or Eq. (4.3.11) may be used to characterize the cooperativity of the system. In the general case (m > 2), one cannot use the form of the BI (or of any of its transformed functions) either to characterize or to define cooperativity. Unfortunately, the characterization of cooperativity by the form (especially of the Hill plot) is still very common in the biochemical literature. [Pg.77]

The palladium-catalyzed coupling of boronic acids with aryl and alkenyl halides, the Suzuki reaction, is one of the most efficient C-C cross-coupling processes used in reactions on polymeric supports. These coupling reactions requires only gentle heating to 60-80 °C and the boronic acids used are nontoxic and stable towards air and water. The mild reaction conditions have made this reaction a powerful and widely used tool in the organic synthesis. When the Suzuki reaction is transferred to a solid support, the boronic add can be immobilized or used as a liquid reactant Carboni and Carreaux recently reported the preparation of the macroporous support that can be employed to efficiently immobilize and transform functionalized arylboronic adds (Scheme 3.12) [107, 246, 247]. [Pg.166]


See other pages where Transformation function is mentioned: [Pg.526]    [Pg.109]    [Pg.127]    [Pg.2083]    [Pg.6]    [Pg.23]    [Pg.718]    [Pg.164]    [Pg.16]    [Pg.51]    [Pg.245]    [Pg.58]    [Pg.10]    [Pg.14]    [Pg.53]    [Pg.204]    [Pg.451]    [Pg.16]    [Pg.33]    [Pg.251]    [Pg.33]   
See also in sourсe #XX -- [ Pg.62 ]

See also in sourсe #XX -- [ Pg.62 ]




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Allyl rearrangement functional group transformation

Aminosilanes functional group transformation

Apodizing functions Fourier transforms

Autocorrelation function Fourier transform

Autocorrelation function Laplace transform

Barton functionalization transform

Best Synthetic Methods Functional Group Transformations

Beyond Functional Croup Transformation

Biotransformations functional group transformation

Canonical transformation theory reference function

Carbonyl compounds functional group transformations

Carbonyl functions, transformation

Causal function Hilbert transform

Cell-containing functional group transformations

Chiral metal complexes functional group transformation

Chlorosilanes functional group transformation

Correlation function transform

Correlation functions Laplace transform

Cosine function Fourier transform

Defect Functionalization - Transformation of Carboxylic Functions

Delta function Fourier transform

Density functional theory Fourier transform

Density functional theory local-scaling transformation

Dirac delta function transformations

Dirac delta function — Fourier transform

Disconnection Using Tactical Sets of Functional Group-Keyed Transforms

Elimination reactions functional group transformations with

Energy transformation function

Example of transformation to HLSP functions

Explicit Transformation Functions

Exponential decay function Fourier transform

Exponential function transform

Exponential function, Laplace transform

Field correlation function Laplace transform

Fourier Transform and Discrete Function Continuation

Fourier transform correlation function

Fourier transform function

Fourier transform function, definition

Fourier transform general EXAFS function

Fourier transform infrared functional groups detection

Fourier transform infrared functions used

Fourier transform infrared spectroscopy functional groups detection

Fourier transform of the -function

Fourier transform of the density correlation function

Fourier transform response function

Fourier transform sine function

Fourier transform wave function properties

Fourier transform, velocity autocorrelation function

Fourier transform-infrared spectroscopy functional group analysis

Fourier transforms of the function

Fourier-Laplace transform, response function

Fourier-transforms (Patterson functions)

Functional Group Transformation by Nucleophilic Substitution Reactions

Functional Group Transformation of Aminosilanes

Functional Group Transformation of Chlorosilanes

Functional Group Transformation of Hydrosilanes

Functional Group Transformations Index

Functional Group Transformations Oxidation and reduction

Functional Group Transformations that Generate Amines

Functional Groups and Appendages as Keys for Connective Transforms

Functional based transforms

Functional group transformation, chiral metal

Functional group transformations

Functional group transformations alkyl halides

Functional group transformations groups

Functional group transformations palladium complexes

Functional group transformations peroxides

Functional groups transformation, by nucleophilic

Functional groups transformation, by nucleophilic substitution

Functions, scaling transformations

Gauge transformation wave functions

Gaussian function Fourier transform

Generating functions of tree graphs and Legendre transformation

Green function Fourier transform

Green function Fourier transforms

Hartree-Fock function transformation

Hubbard-Stratonovich Transformation Field-Theoretic Reformulation of the Particle-Based Partition Function

Hydrosilane functional group transformation

Integral transformation function

Keying element for transform function

Kubo transformed correlation function

Laplace - inverse transform function

Laplace transform Mittag-Leffler function

Laplace transform canonical partition function

Laplace transform function

Laplace transform grand partition function

Laplace transform limit functions

Laplace transform transfer functions

Laplace transform wave function

Laplace transforms of common functions

Laplace transforms of various functions

Laplace transforms ramp function

Laplace transforms step functions

Legendre Transformation and Convex Functions

Microwave-Assisted Functional Group Transformations

Modified Electrodes Switchable by Applied Potentials Resulting in Electrochemical Transformations at Functional Interfaces

Modified z Transforms of Common Functions

Pair correlation function, Fourier transform

Probability Generating Functions in a Transformation Method

Propargylic rearrangements functional group transformation

Pulse function Laplace transform

Pyrans functional group transformations

Rectangular function Fourier transform

Schmidt transformation function

Selecting Reagents to Accomplish Functional Group Transformation

Spectral density function Fourier transform

Step function Laplace transform

Stress autocorrelation function, Fourier transformation

Substitution reactions functional group transformation

Synthesis and functional group transformations

TRANSFORMATIONS THAT GIVE OXYGEN-CONTAINING FUNCTIONAL GROUPS

The Double Functional Group Transformation Terminally Unsaturated

The specific rate function k(E) as an inverse Laplace transform

Thermodynamic Similarity of Transformed Functions

Transform connective, functional groups

Transform functional group interchange

Transform functional group removal , (Chart

Transform functional group transposition

Transform functional group-based

Transform functional group-keyed,

Transform of Distribution Functions

Transformation Properties of the Wave Function

Transformation Using Functional Integral Identities

Transformation functional integral identities

Transformation of Functional Groups

Transformation of functions

Transformations between standard tableaux and HLSP functions

Transformations of the Carbonyl Functions

Transforms Functional group

Transforms of Some Basic Functions

Triangular function Fourier transform

Trigonometric functions Laplace transforms

Useful Properties of Laplace Transform limit functions

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