Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Introduction functions

Figure 9.14 Proteoglycan aggregate found in cartilage. C and N are C and N termini of the core protein. Long wavy lines represent chondroitin sulfate, whereas the short lines represent keratan sulfate. All are linkied to the core protein via the O-serine linkage, except for a few oligosaccharide chains near the N terminus of the core protein. LP is link protein, and HA is hyaluronic acid. (Reproduced by permission from Hascall V. Introduction. Functions of the Proteoglycans, Ciba Foundation Symposium 124. New York Wiley Sons, 1986, p. 2.)... Figure 9.14 Proteoglycan aggregate found in cartilage. C and N are C and N termini of the core protein. Long wavy lines represent chondroitin sulfate, whereas the short lines represent keratan sulfate. All are linkied to the core protein via the O-serine linkage, except for a few oligosaccharide chains near the N terminus of the core protein. LP is link protein, and HA is hyaluronic acid. (Reproduced by permission from Hascall V. Introduction. Functions of the Proteoglycans, Ciba Foundation Symposium 124. New York Wiley Sons, 1986, p. 2.)...
Introduction and commercial application Safety and the environment have become important elements of all parts of the field life cycle, and involve all of the technical and support functions in an oil company. The Piper Alpha disaster in the North Sea in 1988 has resulted in a major change in the approach to management of safety of world-wide oil and gas exploration and production activities. Companies recognise that good safety and environmental management make economic sense and are essential to guaranteeing long term presence in the industry. [Pg.65]

As stated in the introduction to the previous chapter, adsorption is described phenomenologically in terms of an empirical adsorption function n = f(P, T) where n is the amount adsorbed. As a matter of experimental convenience, one usually determines the adsorption isotherm n = fr(P), in a detailed study, this is done for several temperatures. Figure XVII-1 displays some of the extensive data of Drain and Morrison [1]. It is fairly common in physical adsorption systems for the low-pressure data to suggest that a limiting adsorption is being reached, as in Fig. XVII-la, but for continued further adsorption to occur at pressures approaching the saturation or condensation pressure (which would be close to 1 atm for N2 at 75 K), as in Fig. XVII-Ih. [Pg.599]

As mentioned in the introduction, the simplest way of approximately accounting for the geomehic or topological effects of a conical intersection incorporates a phase factor in the nuclear wave function. In this section, we shall consider some specific situations where this approach is used and furthermore give the vector potential that can be derived from the phase factor. [Pg.44]

In an Abelian theory [for which I (r, R) in Eq. (90) is a scalar rather than a vector function, Al=l], the introduction of a gauge field g(R) means premultiplication of the wave function x(R) by exp(igR), where g(R) is a scalar. This allows the definition of a gauge -vector potential, in natural units... [Pg.147]

Better END approximations are defined by the introduction of more general molecular wave functions leading to larger and more involved parameter spaces. [Pg.229]

Next, an attempt was made to evaluate the quantitative importance of the various reaction schemes [19]. To this effect, a printed compilation of 1900 reactions dealing with the introduction of one carbon atom bearing a functional group [20] was analyzed and each reaction assigned manually to a corresponding reaction scheme. The results are Hsted in Table 3-3. [Pg.189]

J. Matthieu, J. Weill-Raynal, Formation of C-C Bonds, Vol. I, Introduction of a Functional Carbon Atom, G. Thieme, Stuttgart, 1973. [Pg.201]

Most database users do not know how the data are organized in a database system (DBS) they depend solely on the application programs. This is sufficient for most database searches where users can receive large amounts of results quickly and easily, e.g., on literature or other information. Nevertheless, a basic knowledge on where and how to find deeper or more detailed information is quite useful. Due to their complex nature, comprehensive searches (e.g., for processes or patents) are not recommended for beginners. However, most local (in-house), online, and CD-ROM databases provide extensive tutorials and help functions that are specific to the database, and that give a substantial introduction into database searching. [Pg.230]

Iris type of constrained minimisation problem can be tackled using the method of Lagrange nultipliers. In this approach (see Section 1.10.5 for a brief introduction to Lagrange nultipliers) the derivative of the function to be minimised is added to the derivatives of he constraint(s) multiplied by a constant called a Lagrange multiplier. The sum is then et equal to zero. If the Lagrange multiplier for each of the orthonormality conditions is... [Pg.72]

In the earlier versions of the streamline upwinding scheme the modified weight function was only applied to the convection tenns (i.e. first-order derivatives in the hyperbolic equations) while all other terms were weighted in the usual manner. This is called selective or inconsistent upwinding. Selective upwinding can be interpreted as the introduction of an artificial diffusion in addition to the physical diffusion to the weighted residual statement of the differential equation. This improves the stability of the scheme but the accuracy of the solution declines. [Pg.54]

This is an introduction to the techniques used for the calculation of electronic excited states of molecules (sometimes called eximers). Specifically, these are methods for obtaining wave functions for the excited states of a molecule from which energies and other molecular properties can be calculated. These calculations are an important tool for the analysis of spectroscopy, reaction mechanisms, and other excited-state phenomena. [Pg.216]

Introduction of Non-functional Alkyl and Reactive Allyl Groups... [Pg.19]

Since (A) does not contain any other functional group in addition to the formyl group, one may predict that suitable reaction conditions could be found for all conversions into (A). Many other alternative target molecules can, of course, be formulated. The reduction of (H), for example, may require introduction of a protecting group, e.g. acetal formation. The industrial synthesis of (A) is based upon the oxidation of (E) since 3-methylbutanol (isoamyl alcohol) is a cheap distillation product from alcoholic fermentation ( fusel oils ). The second step of our simple antithetic analysis — systematic disconnection — will now be exemplified with all target molecules of the scheme above. For the sake of brevity we shall omit the syn-thons and indicate only the reagents and reaction conditions. [Pg.198]

The most difflcult pharmaceutically relevant oxidation of steroids is the introduction of a 14 -hydroxyl group. This functional group is found in heart-active steroids (cardenolides) such as digitoxigenin, which also contain a 17/J-butenolide substituent. The 14/ -hydroxyl group is easily cleaved off by dehydration and must therefore not be treated with Lewis or... [Pg.286]

One of the virtues of the Fischer indole synthesis is that it can frequently be used to prepare indoles having functionalized substituents. This versatility extends beyond the range of very stable substituents such as alkoxy and halogens and includes esters, amides and hydroxy substituents. Table 7.3 gives some examples. These include cases of introduction of 3-acetic acid, 3-acetamide, 3-(2-aminoethyl)- and 3-(2-hydroxyethyl)- side-chains, all of which are of special importance in the preparation of biologically active indole derivatives. Entry 11 is an efficient synthesis of the non-steroidal anti-inflammatory drug indomethacin. A noteworthy feature of the reaction is the... [Pg.61]


See other pages where Introduction functions is mentioned: [Pg.242]    [Pg.597]    [Pg.242]    [Pg.597]    [Pg.421]    [Pg.33]    [Pg.2409]    [Pg.2709]    [Pg.41]    [Pg.124]    [Pg.157]    [Pg.197]    [Pg.231]    [Pg.255]    [Pg.255]    [Pg.344]    [Pg.451]    [Pg.4]    [Pg.14]    [Pg.152]    [Pg.372]    [Pg.444]    [Pg.362]    [Pg.11]    [Pg.395]    [Pg.564]    [Pg.19]    [Pg.21]    [Pg.25]    [Pg.26]    [Pg.154]    [Pg.3]   
See also in sourсe #XX -- [ Pg.2 ]




SEARCH



An Introduction to Density Functional Theory

An Introduction to Potential Functions and Surfaces—Bond Stretches

An Introduction to the Electron Localization Function

Carboxylic function, introduction

Density Functional Theory introduction

Functional groups, introduction

Functional organic group introduction

Functional sites introduction

Introduction and Conversion of Functional Sites on Polymer

Introduction and Interchange of Functional Groups

Introduction of Non-functional Alkyl and Reactive Allyl Groups

Introduction of an Unsaturated Functionality

Introduction of functional

Introduction of functional groups

Introduction of other functional groups

Introduction of oxygen functions and their reactions

Introduction of the Partition Functions

Introduction orthogonality of wave functions

Introduction to Density Functionals

Introduction to Functional Groups

Introduction to Functional Groups and Alcohols

Introduction to Organic Molecules and Functional Groups

Introduction to Radial Basis Functions

Introduction, Occurrence, Structure, Function

Ketone functionality introduction

Key Concepts—Introduction to Organic Molecules and Functional Groups

Methods for Introduction of Fluorine-Functionality into Molecules

Proteins, introduction function, mechanisms

Proteins, introduction function, regulation

Remote functionality introduction

© 2024 chempedia.info