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Synthesis Results

Several metrics are used to measure the area-cost of a design. The area is measured indirectly in terms of how many components are used, the bits of hardware used and the size of the control unit. The metrics are as follows  [Pg.202]

Control Unit The size of the control unit can be estimated by the number of control points required to control the components in the [Pg.202]

Functional Units Total number of bits of functional units, where a functional unit implies combinational logic to implement a function, such as an adder. [Pg.203]

Wiring Units Total number of bits of wiring units, where a wiring unit implies wires that implement a function such as a concatenation of values. [Pg.203]

Interconnections Multiplexors and busses represent actual combinational logic, and imply the degree of interconnection complexity for a design. The complexity can be broken down further by considering the numbers of inputs and outputs of the multiplexors and busses. Since bus inputs require tri-state devices, there is a cost associated with them, while bus outputs may require drivers, which also add to the area of a design. [Pg.203]


It has been known for some time that tetracyclines are accumulated by bacteria and prevent bacterial protein synthesis (Fig. 4). Furthermore, inhibition of protein synthesis is responsible for the bacteriostatic effect (85). Inhibition of protein synthesis results primarily from dismption of codon-anticodon interaction between tRNA and mRNA so that binding of aminoacyl-tRNA to the ribosomal acceptor (A) site is prevented (85). The precise mechanism is not understood. However, inhibition is likely to result from interaction of the tetracyclines with the 30S ribosomal subunit because these antibiotics are known to bind strongly to a single site on the 30S subunit (85). [Pg.181]

Die neurological disorder associated with severe vitamin B12 deficiency is termed funicular myelitis. Vitamin B12 deficiency leads to disturbed choline-, phospholipid-, and nucleic-acid synthesis, resulting in spinal marrow damages. Disturbed myelin synthesis finally causes irreversible neurological failure. In addition, there are psychiatric disturbances (disturbed memory, apathy). [Pg.512]

All defects in urea synthesis result in ammonia intoxication. Intoxication is more severe when the metabolic block occurs at reactions 1 or 2 since some covalent linking of ammonia to carbon has already occurred if citrulline can be synthesized. Clinical symptoms common to all urea cycle disorders include vomiting, avoidance of high-protein foods, intermittent ataxia, irritability, lethargy, and mental retardation. The clinical features and treatment of all five disorders discussed below are similar. Significant improvement and minimization of brain damage accompany a low-protein diet ingested as frequent small meals to avoid sudden increases in blood ammonia levels. [Pg.247]

Eukaryotic mRNA synthesis results in a pre-mRNA precursor that contains extensive amounts of excess RNA (introns) that must be precisely removed by RNA splicing to generate functional, translatable mRNA composed of exonic coding and noncoding sequences. [Pg.357]

Folic acid antagonist inhibits dihydrofolate reductase (DHFR) blocks reduction of folate to tetrahydrofolate inhibits de novo purine synthesis results in arrest of DNA, RNA, and protein synthesis... [Pg.1409]

A marked interference with heme synthesis results in a reduction of the hemoglobin concentration in blood. Decreased hemoglobin production, coupled with an increase in erythrocyte destruction, results in a hypochromic, normocytic anemia with associated reticulocytosis. Decreased hemoglobin and anemia have been observed in lead workers and in children with prolonged exposure at higher PbB levels than those noted as threshold levels for inhibition or stimulation of enzyme activities involved in heme synthesis (EPA 1986a). [Pg.264]

Fig. 4.9 A synthesis resulting in polypeptides (or compounds similar to polypeptides using amino-malonitrile and further adding hydrogen cyanide. In this process, R 15 may represent different side chains of amino acids... Fig. 4.9 A synthesis resulting in polypeptides (or compounds similar to polypeptides using amino-malonitrile and further adding hydrogen cyanide. In this process, R 15 may represent different side chains of amino acids...
The answer is e. (Katzung, p 842.) Ribavirin most likely interferes with guanosine triphosphate synthesis, resulting in inhibition of capping of viral messenger RNA and viral RN A-dependent RNA polymerase. It is effective in moderating infections with respiratory syncytial virus. [Pg.85]

A highly enantioselective dihydropyran synthesis results from the use of bis(oxazoline) copper(II) complexes as catalysts <00JA1635 00JA7936> and the value of this approach to carbohydrate synthesis has been noted . [Pg.320]

The synthesis of 5-HT can increase markedly under conditions requiring more neurotransmitter. Plasticity is an important concept in neurobiology. In general, this refers to the ability of neuronal systems to conform to either short- or long-term demands placed upon their activity or function (see Plasticity in Ch. 53). One of the processes contributing to neuronal plasticity is the ability to increase the rate of neurotransmitter synthesis and release in response to increased neuronal activity. Serotonergic neurons have this capability the synthesis of 5-HT from tryptophan is increased in a frequency-dependent manner in response to electrical stimulation of serotonergic soma [7]. The increase in synthesis results from the enhanced conversion of tryptophan to 5-HTP and is dependent on extracellular calcium ion. It is likely that the increased 5-HT synthesis results in part from alterations in the kinetic properties of tryptophan hydroxylase, perhaps due to calcium-dependent phosphorylation of the enzyme by calmodulin-dependent protein kinase II or cAMP-dependent protein kinase (PKA see Ch. 23). [Pg.233]

Very recently, Reetz, Ma and Goddard reported phosphoramidites based on BINOL bearing a single ortho-substituent (Scheme 28.10) [69]. These ligands are also chiral on phosphorus, such that the synthesis results mostly in diastereo-mers which have to be separated. In several cases, however, one of the diaster-eomers was formed exclusively. Some of the ligands afford high ee-values in the hydrogenation of methyl N-acyl dehydroalanine and dimethyl itaconate. [Pg.1007]

Thin polymer films have been prepared by surface catalysis in ultrahigh vacuum and electrochemical deposition from solution. These two routes of synthesis result in poly(thiophene), poly(aniline) and poly(3,5-lutidine) films that have similar infrared spectra. These polymer films are highly orientationally ordered the rings are perpendicular to the surface in poly(thiophene) and poly(3,5-lutidine) films, and the phenyl rings are parallel to the surface in poly(aniline). [Pg.83]

Ordered mesoporous materials of compositions other than silica or silica-alumina are also accessible. Employing the micelle templating route, several oxidic mesostructures have been made. Unfortunately, the pores of many such materials collapse upon template removal by calcination. The oxides in the pore walls are often not very well condensed or suffer from reciystallization of the oxides. In some cases, even changes of the oxidation state of the metals may play a role. Stabilization of the pore walls in post-synthesis results in a material that is rather stable toward calcination. By post-synthetic treatment with phosphoric acid, stable alumina, titania, and zirconia mesophases were obtained (see [27] and references therein). The phosphoric acid results in further condensation of the pore walls and the materials can be calcined with preservation of the pore system. Not only mesoporous oxidic materials but also phosphates, sulfides, and selenides can be obtained by surfactant templating. These materials have pore systems similar to OMS materials. [Pg.125]

Crystallization of optically active sulflmides 208 and 209 prepared by asymmetric synthesis results in a gradual increase of their melting points and optical rotations until the values given below are attained (138). The failure of successive crystallizations to affect these values... [Pg.403]

Peptides have many desirable properties as components of synthetic vectors. Peptide synthetic chemistry is well established, with the convenience of automated synthesis resulting in a well-defined, high-purity product of low toxicity and immunogenicity for in vivo use. Furthermore, even short peptides of 7 to 30 amino acids can accommodate enormous structural diversity, functionality, and combinations of properties. [Pg.295]

This is a precisely choreographed process. Each stage involves complex regulatory mechanisms to ensure that progress through the cell cycle is accomplished one step at a time, is unidirectional, and permits exactly one round of DNA synthesis, resulting in precise duplication of the cellular chromosomes. It is a beautiful, if complex and not yet fully complete, story. [Pg.341]

In addition, surface-mediated synthesis results a powerful tool in the preparation of surface carbonyl species (homo- or heteronuclear) that are further precursors of supported, tailored metallic catalysts. [Pg.339]

Lastly, we consider Boesten et al. (2001) (excerpt 5E), which describes an asymmetric Strecker synthesis. Recall that the synthesis results in two diastereomers, which can be separated based on their different solubilities in water. In exercise 2.14 (chapter 2), you were asked to decide where the Discussion section began in this article. That exercise was more challenging than you may have realized. The article presents numerous results, with only a few sections of integrated discussion. [Pg.184]

Equations 2-27 and 2-33 and Fig. 2-2 describe the much greater difficulty of performing a successful polymerization compared to the analogous small-molecule reaction (such as the synthesis of ethyl acetate from acetic acid and ethanol). Consider the case where one needs to produce a polymer with a degree of polymerization of 100, which is achieved only at 99% reaction. Running the polymerization to a lower conversion such as 98%, an excellent conversion for a small-molecule synthesis, results in no polymer of the desired molecular weight. Further, one must almost double the reaction time (from 450 min to 850 min in Fig. 2-2) to achieve 99% reaction and the desired polymer molecular weight. For the small molecule reaction one would not expend that additional time to achieve only an additional 1 % conversion. For the polymerization one has no choice other than to go to 99% conversion. [Pg.52]


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Impurities Resulting from the Synthesis Pathway

Polymer synthesis results

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