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Tabulation synthesis

General synthetic methods were developed after 1920 and extended to many new systems. Oxidative syntheses of dyes are primarily of historical interest (1), whereas nonoxidative syntheses are the most versatile and employ varied combinations of nucleophilic and electrophilic regents. One review Hsts references for the synthesis of dyes prepared before 1959 (12), and another review provides supplemental references to more recent compounds (13). Many nucleophilic and electrophilic reagents used to synthesize cyanine and related dyes are tabulated in Reference 16. [Pg.394]

It is appropriate to identify our approach to developing the present review in the context of the Co chapter in CCC(1987). The first-edition chapter on Co featured a focused discussion and tabulation of synthetic methods, and many of these basic methods are still employed in synthesis today. Consequently, to avoid repetition, there will be diminished description here where prior appropriate methods have been provided, and only newer developments featured. The last two decades feature the development of many mixed-donor and sophisticated multidentate and macrocyclic ligands, which found limited coverage in the previous edition, and these will be discussed in more detail herein. Reaction kinetics and mechanism were also described thoroughly in the previous edition. We shall not reiterate this material, since the core mechanisms of many reactions involving Co compounds are now adequately defined. [Pg.3]

For the gas phase synthesis of phosgene, CO + Cl2 => C0C12, A + B => C, the tabulated data were obtained at 25°C with starting pressure of 4.0 torr for CO. and two different pressures for Cl2 t is in minutes and the partial pressures are in torr. Find the rate equation. Check the rate equation. [Pg.172]

In contrast, tellurium insertion in alkyl- or aryllithium compounds followed by alkylation is a useful method for the synthesis of unsymmetrical tellurides. (For a tabulation of unsymmetrical tellurides prepared by alkylation of organyl tellurolates, see ref. 8.)... [Pg.25]

It would require a Herculean effort to prepare a complete discussion and review of every report related to the synthesis, reaction, or application of an oxazole while tabulating every oxazole, oxazolone, oxazoline, and chiral bis(oxazoline) prepared and evaluated during the period of 1983-2001. Such an undertaking is beyond the scope of this review. Furthermore, the ease with which electronic databases, including the patent literature, can be searched, the data retrieved, and the information tabulated would render such a project somewhat redundant. [Pg.705]

Over 20 transferases have now been cloned [12], Other glycosyltransferases can be obtained from readily available tissue sources in at least milliunit amounts, which is sufficient for milligram-scale synthesis. These are tabulated in a recent review [13]. [Pg.489]

The yields obtained in the oxidation of several oxaziranes are tabulated in Table 4. The synthesis of nitrusoalkanee via oxazirape intermediates... [Pg.589]

Tertiary phosphines form a wide range of complexes of the type PtX2(PR3)2 (X - halide, pseudohalide R = alkyl, aryl or mixed alkylaryl). Space limitations preclude this chapter becoming a compendium of known compounds, therefore for each individual complex the reader is directed to Chemical Abstracts, Gmelin or the book by McAuliffe which contains extensive tabulations of compounds.1225 In this chapter we outline the general methods of synthesis, the properties, and the structures and spectral features which we expect to be found with this class of compounds. [Pg.445]

A broad variety of l.c. polymers is conceivable because of the wide range of well known mesogenic molecules, e.g. tabulated in the book of Dcmus27), and the different types of polymers. Further variations are possible by copolymers or systems, where each monomer unit carries more than one mesogenic moiety ( en bloc systems28)). Furthermore the synthesis of linear, branched and crosslinked systems has to be mentioned. Because of this broad variety a manifold influence on the phase behavior of the systems via the chemical constitution is feasible. In the following chapter we will discuss some basic considerations on the phase behavior of l.c.-side chain polymers. [Pg.106]

Specifications. The specifications for ethyl alcohol are designed with sufficient latitude to allow for the two principal means of production, synthesis from ethylene and fermentation. The requirements given by the U.S. Pharmacopeia (USP) and the American Chemical Society (ACS) generally form the foundation for the most widely used specifications (255,256). A tabulation of the specifications from the major alcohol producers, with consideration for the USP and ACS requirements, is shown in Table 5. [Pg.412]

This solution has the advantage of being very simple, but the drawback of being expensive in terms of calculations, even when tabulated sinusoids are used in Eq. (7.17). In fact, additive synthesis (of which Eq. (7.17) is an example) can be implemented at a much lower cost by use of the Fourier transform [Rodet and Depalle, 1992]. This last remark is a strong motivation for using the following alternative ... [Pg.161]

Metrics for music synthesis techniques in the past have been dominated by simple tabulations of CPU costs or brief subjective evaluations of sound quality. Recently, efforts have been made to apply metrics to many aspects of synthesis techniques [Jaffe, 1995], While it may be difficult to exactly define metrics for some of the subjective elements of synthesis techniques, it is still very helpful to try to apply metrics for evaluating different methods of synthesis. Two of the most important metrics could be accuracy and expressivity. [Pg.173]

The format follows that of the earlier review. The subject of synthesis, however, which formerly constituted a separate chapter, is included in this work, and other coverage has been expanded, particularly in the areas of plant biochemistry and pharmacology. The tabulation of all known bisbenzylisoquinoline alkaloids has been revised and updated. A section listing other major review articles on these alkaloids is also included, and the reader may wish to consult some of these for extensive physical data. In keeping with the original purpose of this treatise, we have tried for a comprehensive overview, with strong emphasis on the specific chemistry of the bisbenzylisoquinoline alkaloids, rather than an exhaustively detailed presentation. [Pg.2]

H. Guinaudeau, M. Leboeuf, and A. Cave, J. Nat. Prod. 42, 133 (1979). Dimeric aporphine-benzylisoquinoline and aporphine-pavine alkaloids. Tabulates physical properties, sources, and references to synthesis of 28 alkaloids. [Pg.155]

NCs is indispensable. In the case of cadmium chalcogenide NCs, the concentration of a colloidal solution can be determined in good approximation by means of UV-vis absorption spectroscopy thanks to tabulated relationships between the excitonic peak, the NC size, and the molar absorption coefficient.96 An advanced approach for shell growth derived from chemical bath deposition techniques and aiming at the precise control of the shell thickness is the so-called SILAR (successive ion layer adsorption and reaction) method.97 It is based on the formation of one monolayer at a time by alternating the injections of cationic and anionic precursors and has been applied first for the synthesis of CdSe/CdS CS NCs. Monodispersity of the samples was maintained for CdS shell thicknesses of up to five monolayers on 3.5 nm core CdSe NCs, as reflected by the narrow PL linewidths obtained in the range of 23 to 26 nm FWHM. [Pg.169]

The photochemical reactions of naphthoquinones and quinolinediones with 1,1-diarylethenes have led to the synthesis of many new polycyclic aromatic and heteroaromatic compounds. A review has appeared16 in which a number of these results are tabulated. [Pg.921]

Table 2 Nuclear receptors (NR) for enzyme inducers. Enzyme inducers are now known to act as ligands to nuclear receptors, leading to gene activation and increased synthesis of the enzyme. Affinity of inducers to die receptors is now known to be responsible for the differential induction potential and can explain die observed species-differences in induction. The receptors tabulated are aryl hydrocarbon receptors (AhR), constituitively androstane receptor (CAR), pregnane X receptor (PXR), and glucocorticoid receptor (GR). The isoforms in bold type are the major isoform regulated by the corresponding receptors. Table 2 Nuclear receptors (NR) for enzyme inducers. Enzyme inducers are now known to act as ligands to nuclear receptors, leading to gene activation and increased synthesis of the enzyme. Affinity of inducers to die receptors is now known to be responsible for the differential induction potential and can explain die observed species-differences in induction. The receptors tabulated are aryl hydrocarbon receptors (AhR), constituitively androstane receptor (CAR), pregnane X receptor (PXR), and glucocorticoid receptor (GR). The isoforms in bold type are the major isoform regulated by the corresponding receptors.
A. C. Weedon, in W. M. Horspool (ed.), Synthetic Organic Photochemistry, Plenum (1984). This review covers the use of enone photochemical cycioadditions in organic synthesis, with extensive tabulated data and many synthetic strategies. [Pg.42]

Physical Methods and Physical Chemistry.—Physical diet hods, e.g. chromatographic and spectroscopic techniques, are used routinely in the separation, purification, and characterization of carotenoids and related compounds, and of intermediates in their synthesis. This section will consider only those papers which are devoted largely or entirely to detailed study or analysis of such physical techniques, or which include systematic surveys, often with tabulated data. [Pg.162]


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See also in sourсe #XX -- [ Pg.212 ]




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