Big Chemical Encyclopedia

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

Articles Figures Tables About

Roles in CLASSIC

The purpose of this article is to review recent results on the carbonylation chemistry of actinide-to-carbon sigma bonds, bearing in mind the unique properties of 5f-organometallics cited above. We focus our attention on the properties of bis(pentamethylcyclopentadienyl) actinide acyls. Just as transition metal acyls (A) occupy a pivotal role in classical carbonylation chemistry, it will be seen that many of the unusual... [Pg.60]

A high-resolution structure of a native enzyme is an admirable basis for any mechanistic study relating activity to precise details of structure. It is even better when structures of complexes with substrates and intermediates are available, as is the case with the tyrosyl-tRNA synthetase and tyrosyl adenylate (Figure 15.1). The E Tyr-AMP complex has two remarkable features. The first is the absence of groups that are candidates for roles in classical catalysis. The second is the... [Pg.223]

In a number of classic papers Hohenberg, Kohn and Sham established a theoretical framework for justifying the replacement of die many-body wavefiinction by one-electron orbitals [15, 20, 21]. In particular, they proposed that die charge density plays a central role in describing the electronic stnicture of matter. A key aspect of their work was the local density approximation (LDA). Within this approximation, one can express the exchange energy as... [Pg.95]

Dynorphin may also influence nociception at the spinal level. The levels of prodynorphin mRNA and immunoreactive dynorphin increase in the chronic inflammatory arthritic model (158). Dynorphin also inhibits morphine or P-endorphin-induced analgesia in naive animals and enhances analgesia in tolerant animals, indicating that this peptide may have a regulatory role in opioid analgesia (159). This effect does not appear to be mediated by a classical opioid receptor, since des-tyrosine dynorphin, which does not bind to opioid receptors, also antagonizes morphine analgesia (160). [Pg.450]

Reduction of oxygen is one of the predominant cathodic reactions contributing to corrosion. Awareness of the importance of the role of oxygen was developed in the 1920s (19). In classical drop experiments, the corrosion of iron or steel by drops of electrolytes was shown to depend on electrochemical action between the central relatively unaerated area, which becomes anodic and suffers attack, and the peripheral aerated portion, which becomes cathodic and remains unattacked. In 1945 the linear relationship between rate of iron corrosion and oxygen pressure from 0—2.5 MPa (0—25 atm) was shown (20). [Pg.278]

In classic electro-thermal atomizer the process of formation of the analytical signal is combination of two processes the analyte supply (in the process of evaporation) and the analyte removal (by diffusion of the analyte from the atomizer). In double stage atomizer a very significant role plays the process of conductive transfer of the analyte form the evaporator to the atomizer itself and this makes the main and a principle difference of these devices. Additionally to the named difference arises the problem with optimization of the double stage atomizer as the amount of design pai ameters and possible combination of operation pai ameters significantly increases. [Pg.84]

Further support for this approach is provided by modern computer studies of molecular dynamics, which show that much smaller translations than the average inter-nuclear distance play an important role in liquid state atom movement. These observations have conhrmed Swalin s approach to liquid state diffusion as being very similar to the calculation of the Brownian motion of suspended particles in a liquid. The classical analysis for this phenomenon was based on the assumption that the resistance to movement of suspended particles in a liquid could be calculated by using the viscosity as the frictional force in the Stokes equation... [Pg.293]

A2) In spite of the high individual frequencies, bond length and bond angle vibrations participate in quasi-classical low frequency collective normal modes. Bond angle bending is necessary for the flexibility of five-membered rings, which plays a key role in the polymorphism of nucleic acids. [Pg.118]

II should noi be overlooked that platinum has played a crucial role in ihe development of many branches of science even though the amounts of metal involved may have been small. Reliable Pt crucibles were vital in classical analysis on which the foundations of chemistry were laid. It was also widely used in the development of the electric telegraph, incandescent lamps, and thermionic valves. [Pg.1148]

In conclusion, the Hofmann-Loffler-Freytag reaction tends to give moderate and sometimes poor yields for the preparation pyrrolidines under the classic conditions. Nonetheless, the utility of this reaction to functionalize molecules via the aminyl radical mechanism plays an unique role in the tool box for the organic chemist, enabling transformations not easily achievable using other means. Furthermore, milder conditions and better yields can be achieved by taking advantages of the newer developments such as the Suarez modification. [Pg.95]

The hydrogen atom, containing a single electron, has played a major role in the development of models of electronic structure. In 1913 Niels Bohr (1885-1962), a Danish physicist, offered a theoretical explanation of the atomic spectrum of hydrogen. His model was based largely on classical mechanics. In 1922 this model earned him the Nobel Prize in physics. By that time, Bohr had become director of the Institute of Theoretical Physics at Copenhagen. There he helped develop the new discipline of quantum mechanics, used by other scientists to construct a more sophisticated model for the hydrogen atom. [Pg.137]

Schemes 3-7 describe the synthesis of cyanobromide 6, the A-D sector of vitamin Bi2. The synthesis commences with an alkylation of the magnesium salt of methoxydimethylindole 28 to give intermediate 29 (see Scheme 3a). The stereocenter created in this step plays a central role in directing the stereochemical course of the next reaction. Thus, exposure of 29 to methanol in the presence of BF3 and HgO results in the formation of tricyclic ketone 22 presumably through the intermediacy of the derived methyl enol ether 30. It is instructive to point out that the five-membered nitrogen-containing ring in 22, with its two adjacent methyl-bearing stereocenters, is destined to become ring A of vitamin Bi2. A classical resolution of racemic 22 with a-phenylethylisocyanate (31) furnishes tricyclic ketone 22 in enantiomerically pure form via diaster-eomer 32. Schemes 3-7 describe the synthesis of cyanobromide 6, the A-D sector of vitamin Bi2. The synthesis commences with an alkylation of the magnesium salt of methoxydimethylindole 28 to give intermediate 29 (see Scheme 3a). The stereocenter created in this step plays a central role in directing the stereochemical course of the next reaction. Thus, exposure of 29 to methanol in the presence of BF3 and HgO results in the formation of tricyclic ketone 22 presumably through the intermediacy of the derived methyl enol ether 30. It is instructive to point out that the five-membered nitrogen-containing ring in 22, with its two adjacent methyl-bearing stereocenters, is destined to become ring A of vitamin Bi2. A classical resolution of racemic 22 with a-phenylethylisocyanate (31) furnishes tricyclic ketone 22 in enantiomerically pure form via diaster-eomer 32.
Several nonconventional cadherins that contain cadherin repeats have been described but they have specific features not found in the classical cadherins [1]. The cadherin Flamingo, originally detected in Drosophila, contains seven transmembrane segments and in this respect resembles G protein-coupled receptors. The extracellular domain of Flamingo and its mammalian homologs is composed of cadherin repeats as well as EGF-like and laminin motifs. The seven transmembrane span cadherins have a role in homotypic cell interactions and in the establishment of cell polarity. The FAT-related cadherins are characterized by a large number of cadherin repeats (34 in FAT and 27 in dachsous). Their cytoplasmic domains can bind to catenins. T- (=truncated-)cadherin differs from other cadherins in that it has no transmembrane domain but is attached to the cell membrane via a glycosylpho-sphatidylinositol anchor. [Pg.307]

The cytoplasmic domains of protocadherins are unrelated to those of classical cadherins. They do not bind catenins and it is not clear whether they are associated with the cytoskeleton [1]. Some protocadherins interact with the c- src-related kinase Fyn, indicating a role in signal transduction (see below). [Pg.307]

PARs are coupled to multiple G-proteins and mediate a number of well-defined cellular responses via classical second messenger and kinase pathways. PARs are differentially expressed in cells of the vasculature as well in the brain, lung, gastrointestinal tract, skin as well as other highly vascularised tissues and evidence suggests distinct physiological functions and roles in disease states [2]. [Pg.1020]

These two amphoteric rules play an important role both in classical and in electrochemical promotion as further discussed at the end of this Chapter and in the mathematical modeling of Chapter 6. [Pg.62]


See other pages where Roles in CLASSIC is mentioned: [Pg.227]    [Pg.558]    [Pg.80]    [Pg.2]    [Pg.102]    [Pg.240]    [Pg.227]    [Pg.558]    [Pg.80]    [Pg.2]    [Pg.102]    [Pg.240]    [Pg.189]    [Pg.78]    [Pg.398]    [Pg.871]    [Pg.994]    [Pg.3033]    [Pg.370]    [Pg.657]    [Pg.135]    [Pg.142]    [Pg.342]    [Pg.128]    [Pg.90]    [Pg.16]    [Pg.625]    [Pg.411]    [Pg.135]    [Pg.211]    [Pg.256]    [Pg.257]    [Pg.308]    [Pg.516]    [Pg.640]    [Pg.824]    [Pg.1114]    [Pg.1114]    [Pg.10]    [Pg.272]   
See also in sourсe #XX -- [ Pg.49 ]




SEARCH



© 2024 chempedia.info