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Figure 22 represents the main consequences on pyrazole reactivity when a positive charge is present at the 2-position of the nucleus. A similar situation occurs in the indazolium salts, which thermally decompose into an alkylindazole and an alkyl halide, a reaction sequence described by von Auwers. [Pg.217]

Microprocessors are tbe latest technology in the field of p.f. correction. Switching can be programmed through any of the switching sequences described above. Correction now is much faster, as noted already. [Pg.771]

Figure 2.11. The sequence described in the text for (a) Eulerian and (b) Lagrangian coordinates. Hashmarks indicate material particle positions. Figure 2.11. The sequence described in the text for (a) Eulerian and (b) Lagrangian coordinates. Hashmarks indicate material particle positions.
Like Thr 124 and Thr 215, the Asn 69 and Asn 159 residues occupy equivalent positions in the two homologous motifs of TBP. By analogy with the symmetric binding of a dimeric repressor molecule to a palindromic sequence described in Chapter 8, the two motifs of TBP form symmetric sequence-specific hydrogen bonds to the quasi-palindromic DNA sequence at the center of the TATA box. The consensus TATA-box sequence has an A-T base pair at position 4, but either a T-A or an A-T base pair at the symmetry-related position 5, and the sequence is, therefore, not strictly palindromic. However, the hydrogen bonds in the minor groove can be formed equally well to an A-T base pair or to a T-A base pair, because 02 of thymine and N3 of adenine occupy nearly stereochemically equivalent positions, and it is sufficient, therefore, for the consensus sequence of the TATA box to be quasi-palindromic. [Pg.158]

The synthesis of prostaglandin Ei in the naturally occurring leva form was achieved by a modification of the sequence described above in which the racemic amine A was resolved with (-)-oc-bromocamphor-Tt-sulfonic acid. The enantiomer of the natural PGEi ([a]57g+57° (cO.5, THE)) was also synthesized (Ref. 3). [Pg.254]

B-Homosteroids were first reported by Ringold in the course of an investigation of the relationship of structural changes to biological activity of anabolic agents. The Tiffeneau rearrangement sequence described earlier for the preparation of A-homosteroids was used to synthesize 17/ -hydroxy-B-homo-5a-androstan-3-one (56a). [Pg.374]

To understand how the chemical shift and multiplicity information is separated, we need to reconsider the spin-echo sequence described earlier. [Pg.214]

The key intermediates 116 and 117 were coupled by the three-step sequence described above for the model system (Scheme 3.25). Thus, treatment of a mixture of 116 and 117 with TASF(Et) formed the coupling product 136 in 79 % yield. We rationalize the regioselectivity of the coupling step by considering the electronic... [Pg.62]

The orthometallation-carbonylation sequence described earlier (Scheme 155) has been used to effect regiospecific methoxycarbonylation of 4-thiachromanones (Scheme 161 ).232... [Pg.391]

Generation of an initial population of random separation sequences is done first. The sequences describe both which equipment items are used and how they are connected. [Pg.111]

The generation of an initial population of random separation sequences is done first. The sequences describe both in which order the components are separated and which separation method is used. For example the sequence on left in Figure 13 is described by the string 23 12 14 11. The first integer is for the separation method and the second for the heavy key component of the split in the column. The first separation is made by method 2 and the components heavier than no.3 (i.e. 4 and 5) go to bottom. In the next separation method 1 is used and component heavier than 2 (i.e. 3) goes to bottom, etc. [Pg.113]

Suppose that the following sequence describes the reactions of two different substrates catalyzed by one enzyme ... [Pg.856]

Up to this point, we have ignored the effect of h during the rf pulses. Of course, if h << H], then the effect is negligible. But in the case of very broad lines where h for many of the nuclear moments in the sample, the effect becomes very significant. The analytical solution to Equation 1 under these conditions is very complicated. In effect, the pulse sequence described above still produces a spin echo (as can be seen in... [Pg.383]

Fig. 10.14. Gradient-enhanced HMQC pulse sequence described in 1991 by Hurd and John derived from the earlier non-gradient experiment of Bax and Subramanian. For 1H-13C heteronuclear shift correlation, the gradient ratio, G1 G2 G3 should be 2 2 1 or a comparable ratio. The pulses sequence creates heteronuclear multiple quantum of orders zero and two with the application of the 90° 13C pulse. The multiple quantum coherence evolves during the first half of ti. The 180° proton pulse midway through the evolution period decouples proton chemical shift evolution and interchanges the zero and double quantum coherence terms. Antiphase proton magnetization is created by the second 90° 13C pulse that is refocused during the interval A prior to detection and the application of broadband X-decoupling. Fig. 10.14. Gradient-enhanced HMQC pulse sequence described in 1991 by Hurd and John derived from the earlier non-gradient experiment of Bax and Subramanian. For 1H-13C heteronuclear shift correlation, the gradient ratio, G1 G2 G3 should be 2 2 1 or a comparable ratio. The pulses sequence creates heteronuclear multiple quantum of orders zero and two with the application of the 90° 13C pulse. The multiple quantum coherence evolves during the first half of ti. The 180° proton pulse midway through the evolution period decouples proton chemical shift evolution and interchanges the zero and double quantum coherence terms. Antiphase proton magnetization is created by the second 90° 13C pulse that is refocused during the interval A prior to detection and the application of broadband X-decoupling.
Such an example has been recently worked out, combining a very hard block i.e. polypivalolactone (PPVL), with a thermostable elastomer segment i.e. polydimethyl-siloxane (PDMS), using the reactions sequence described in scheme 3. (One should note that the starting PDMS has been obtained through a previously described procedure (14), avoiding any unstable Si-O-C bond in the final produc t). [Pg.312]

The efficient addition-cyclization sequence described above could be successfully applied to the preparation of the polyhydroxylated y-amino acid (-)-detoxinine [73], The crucial key step in this fairly short synthesis is the chelate-controlled addition of lithiated benzyloxyallene 120 (R = Bn) to the chiral N-benzyl-substituted imine 121 as shown in Scheme 8.31. The required skeleton of the natural product was generated in good overall yield. [Pg.445]

Phenyl-1-pyrroline is useful for various purposes.10 11 In particular, its reduction product, 2-phenylpyrrolidine, is important in the synthesis of pyrroloisoquinoline antidepressants,20 12 and can be a starting point in alkaloid synthesis.13 The overall reaction sequence described here has been used to prepare nicotine derivatives such as myosmine.2a b... [Pg.257]

Dendrimers have a star-like centre (functionality e.g. 4) in contrast to a star however, the ends of the polymer chains emerging from the centre again carry multifunctional centres that allow for a bifurcation into a new generation of chains. Multiple repetition of this sequence describes dendrimers of increasing generation number g. The dynamics of such objects has been addressed by Chen and Cai [305] using a semi-analytical treatment. They treat diffusion coefficients, intrinsic viscosities and the spectrum of internal modes. However, no expression for S(Q,t) was given, therefore, up to now the analysis of NSE data has stayed on a more elementary level. [Pg.186]

In order to understand this, consider that in an FFC experiment the amplitudes of the acquired signals are approximately proportional to the signal acquisition field Ba- For example, in the case of the basic prepolarized sequence (described in Section VIII.C.), one can show (65) that... [Pg.433]

The primer sequences described here are specific to the Novagen Ek/LIC system and its related suite of vectors, they cannot be used with other, unrelated vectors in the Lie protocols. [Pg.27]

For cationic polymerization with an acid whose anion Z is nucleophilic, initiation involves the sequence described by Eq. 7-51 plus the formation of XXIX. XXIX propagates by a sequence similar to that described by Eqs. 7-52 and 7-53 except that a growing polymer chain possesses a Z—CO— end group instead of a lactam end group. [Pg.571]


See other pages where Sequences describing is mentioned: [Pg.34]    [Pg.436]    [Pg.548]    [Pg.667]    [Pg.704]    [Pg.940]    [Pg.500]    [Pg.704]    [Pg.940]    [Pg.272]    [Pg.729]    [Pg.391]    [Pg.423]    [Pg.125]    [Pg.371]    [Pg.372]    [Pg.98]    [Pg.289]    [Pg.330]    [Pg.463]    [Pg.24]    [Pg.100]    [Pg.12]    [Pg.17]    [Pg.205]    [Pg.116]    [Pg.101]    [Pg.515]    [Pg.186]   
See also in sourсe #XX -- [ Pg.40 ]




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