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Sequence follower

The compile off/on command also allows other non-synthesizable constructs to be implemented. [Pg.225]

This section presents an example that demonstrates some of the more advanced topics in VHDL. These not only include language constructs but also techniques tfiat are useful for design state madiines and control logic in general. The aspects of sequential logic design witfi VHDL that were introduced in Chapter 5 are assumed to be understood at this stage. Topics covered in this section include  [Pg.225]

Instead of presenting a wide variety of different architectures, as in die previous three chapters, a more detailed example is given, which presents the new topics using only two designs. [Pg.225]

A sequence follower circuit watches the sequence of numbers it receives and indicates, through an output signal, when a particular sequence has been received. This example applies this principle to a particular application - a keypad-operated door lock. [Pg.225]

After the enabler has received a reset pulse it will wait to receive four sequence pulses on S from the decoder. If it receives these, it unlocks the door and lights the LED. If a reset pulse is received at any time the counter is reset [Pg.226]


Modem methods of peptide sequencing follow a strategy similar to that used to sequence insulin but are automated and can be carried out on a small scale A key feature is repetitive N terminal identification using the Edman degradation... [Pg.1151]

Nordstrandite. Tlie x-ray diffraction pattern of an aluininum tiiliydroxide wliich differed from the patterns of gibbsite and bayerite was pubhshed (4) prior to the material, named nordstrandite, being found in nature. Tlie nordstrandite structure is also assumed to consist of double layers of hydroxyl ions and aluininum occupies two-tliirds of the octaliedral interstices. Two double layers are stacked with gibbsite sequence followed by two double layers in bayerite sequence. [Pg.169]

There are three possible arrangements of atoms in a layer of SiC crystal, and each type has the same layers but a different stacking sequence (29). Designation (30) is by the number of layers in the sequence, followed by H, R, or C to indicate whether the type belongs to the hexagonal, rhombohedral, or cubic class. [Pg.464]

The OWR protective systems were modeled with event tree diagrams for the time sequence following an initiating event to fuel damage or safe shutdown. Fault trees were used to find the probability of failure of each protective system in a particular event tree. [Pg.427]

The Limerick analysis accounted for a revised list of incident Initiators based on the Limerick plant design and a more detailed analytical modeling of event sequences following each incident initiator. Plant-design-specific and site-specific data were also included in the analysis of the Limerick Mark II containment and in the meterology and demography imput to the evaluation of incident consequences. [Pg.120]

The Reissert method15—conversion of an isoquinoline to a 2-benzoyl-1,2-dihydroisoquinaldonitrile (Reissert compound), alkylation, and hydrolysis—has enjoyed wide success in the synthesis of benzyliso-quinoline and related alkaloids.16,17 In particular, aporphines are prepared conveniently by converting isoquinolines to I-(o-nitrobcnzyl)-isoquinolines via a Reissert sequence, followed by A7-alkylation, reduction, and Pschorr cyclization.17... [Pg.23]

Condensation of 2-aminothiophenol with the /3-chlorocinnamaldehyde in the presence ofp-toluene sulfonic acid (PISA) gave good yield of benzothia-zole (Scheme 14). The mechanism suggested in this work is beUeved to proceed via a nucleophilic attack of the sulfur atom in an addition-ehmination sequence followed by a spontaneous cyclization and ejection of acetaldehyde [15]. These investigations were performed in a domestic microwave reactor and need 1.5 min for completion (65% yield). Here again, oil bath heating seems to be inferior, providing a maximum conversion of 53% after... [Pg.68]

Synthesis of 2-heterocyclic thiosemicarbazones can be summarized in three reaction sequences following the lead of Klayman et al. [5]. Condensation of equimolar quantities of a thiosemicarbazide and a 2-heterocyclic aldehyde or ketone in an alcoholic solvent is represented by Eq. (1). The product s superscripts refer to positions of substitution in the thiosemicarbazone moiety in accord with lUPAC. [Pg.10]

Figure 56.2 Synthetic sequence followed by students for the synthesis of catalysts for evaluation. Bis(trifluoromethyl) derivative (6h) was prepared by the procedure ofLeazer etal. ... Figure 56.2 Synthetic sequence followed by students for the synthesis of catalysts for evaluation. Bis(trifluoromethyl) derivative (6h) was prepared by the procedure ofLeazer etal. ...
These results demonstrate that hole transfer between guanines over short and long (A T)n sequences follow different distance dependencies and there-... [Pg.48]

A typical sequence followed in this test series consists in injecting (1) a micellar slug of one pore volume of aqueous solution of 4% of the preceding pseudobinary system (2% sulfonate/2% Genapol) (2) a slug of desorbent solution corresponding to a fixed amount of additive (e.g. equal to 1 PV at a concentration of 0.5 %) (3) at least 1.5 PV of brine with no additive. [Pg.282]

The hydrogenated (H) block copolymers will be designated by giving the butadiene (B) or isoprene (i) block sequence followed by a number which represents the total weight percentage of butadiene in the polymer. For example HBIB-27 is a hydrogenated triblock copolymer of butadiene-isoprene-butadiene which contains 27% butadiene. Since the polymer is symmetric, the relative composition of each block is therefore 13.5% B -73% I -13.5% B. [Pg.123]

Fig. 4.3. An approximate profile of the free element content of the cytoplasm of all organisms -the free metallome. Downward arrows show outward pumps. Note how closely the sequence follows the inverse of the Irving-Wilhams binding constant sequence (see Appendix 4A). Fig. 4.3. An approximate profile of the free element content of the cytoplasm of all organisms -the free metallome. Downward arrows show outward pumps. Note how closely the sequence follows the inverse of the Irving-Wilhams binding constant sequence (see Appendix 4A).
Assuming that the same adsorption order would occur when these counterions are adsorbed onto the MCC sols used here, this coagulating sequence follows the adsorption order nicely. [Pg.381]

The corresponding endoperoxides of furans usually ring-open to afford 1,4-diketones. Such a sequence, followed by an intramolecular Diels Alder reaction was utilized in the synthesis of the tts-indacenyl dianion (6.7) 613>. [Pg.74]

Fig. 10.15. Pulse sequence for the multiplicity-edited gradient HSQC experiment. Heteronuclear single quantum coherence is created by the first INEPT step within the pulse sequence, followed by the evolution period, t . Following evolution, the heteronuclear single quantum coherence is reconverted to observable proton magnetization by the reverse INEPT step. The simultaneous 180° XH and 13C pulses flanked by the delays, A = l/2( 1 edits magnetization inverting signals for methylene resonances, while leaving methine and methyl signals with positive phase (Fig. 16A). Eliminating this pulse sequence element affords a heteronuclear shift correlation experiment in which all resonances have the same phase (Fig. 16B). Fig. 10.15. Pulse sequence for the multiplicity-edited gradient HSQC experiment. Heteronuclear single quantum coherence is created by the first INEPT step within the pulse sequence, followed by the evolution period, t . Following evolution, the heteronuclear single quantum coherence is reconverted to observable proton magnetization by the reverse INEPT step. The simultaneous 180° XH and 13C pulses flanked by the delays, A = l/2( 1 edits magnetization inverting signals for methylene resonances, while leaving methine and methyl signals with positive phase (Fig. 16A). Eliminating this pulse sequence element affords a heteronuclear shift correlation experiment in which all resonances have the same phase (Fig. 16B).
The most probable mechanism for the reduction requires the initial nucleophilic attack by the hydridometal complex on the nitro group, followed by intramolecular cyclization and extrusion of carbon dioxide. Repetition of the cyclization and extrusion sequence, followed by proton transfer, leads to aniline (Scheme 11.6). [Pg.502]

Primers are used for direct sequencing following amplification from genomic DNA, unless otherwise indicated. PCR, polymerase chain reaction. [Pg.49]

The chemical details of the reaction sequence following HO radical addition and abstraction from olefins should be explored fully— ... [Pg.31]


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Decoder, sequence follower

Enabler sequence follower

Library selection sequence follower

Logic sequence follower

Reset sequence follower

Sequence follower overview

Sequence follower summary

Sequence follower synthesis / optimization

State diagram, sequence follower

State machine sequence follower

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