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Selective transfer

The tetradifferentiated P-cylodextrins 55b-g have been obtained in low yields, about 1% from the native cyclodextrin 2, after purification by HPLC for each step. Even if the method is selective, it is difficult to obtain appreciable quantities of products. [Pg.262]

Direct functionalization of cyclodextrins appears to be efficient on a-cyclodextrin for the synthesis of 6A,6C,6E and 6A,6B,6D,6E patterns of functionality, but was [Pg.262]


Normalize both the input and the target output data to fit the transfer function range. This implies that the data have to be scaled to fit between the minimum and maximum values of the selected transfer function. [Pg.9]

This is a one step economical process for selectively transferring a high quality image to a plastic product. A heated die transfers the pattern from selected transfer tape to a flat plastic surface. Lettering or decorative designs can be transferred in pigmented, wood grain, or metallic finishes. [Pg.545]

The procedure described here illustrates the preparation of mixed lithium arylhetero(alkyl)cuprate reagents and their reactions with carboxylic acid chlorides,4 These mixed cuprate reagents also react with a,a -dibromoketones,12 primary alkyl halides,4 and a,/3-unsaturated ketones,4 with selective transfer of only the alkyl group. [Pg.126]

Interest in anionic polymerizations arises in part from the reactivity of the living carbanionic sites4 7) Access can be provided to polymers with a functional chain end. Such species are difficult to obtain by other methods. Polycondensations yield ro-functional polymers but they provide neither accurate molecular weight control nor low polydispersity. Recently Kennedy51) developed the inifer technique which is based upon selective transfer to fit vinylic polymers obtained cationically with functions at chain end. Also some cationic ring-opening polymerizations52) without spontaneous termination can yield re-functional polymers upon induced deactivation. Anionic polymerization remains however the most versatile and widely used method to synthesize tailor made re-functional macromolecules. [Pg.155]

The selective INEPT experiment also requires a separated proton resonance for excitation and also uses rectangular soft pulses (Bax and Freeman, 1982). Magnetization is selectively transferred by the soft proton pulses to the corresponding carbons to which the protons are coupled. [Pg.373]

Table 2.1 Selected transfer hydrogenation data of R R C=0, R = alkyl, phenyl, R = alkyl, H or... Table 2.1 Selected transfer hydrogenation data of R R C=0, R = alkyl, phenyl, R = alkyl, H or...
These results indicate that (1) the selective transfer of Na from NB to W occurs even when W contains only FMN (in the absence of O2 and pyruvic acid), (2) the existence of FMN, O2, and pyruvic acid and in W and DMFC and Na in NB is necessary for the spontaneous evolution of CO2, and (3) although the coexistence of O2 enhances the transfer of Na, the transfer is independent of pyruvic acid. [Pg.497]

Another type of mixed cyanocuprate has both methyl and alkenyl groups attached to copper. Interestingly, these reagents selectively transfer the alkenyl group in conjugate addition reactions.16 These reagents can be prepared from alkynes via hydrozirconation, followed by metal-metal exchange.17... [Pg.679]

Koning, G.A., Morselt, H.W., Velinova, M.J., Donga, J., Gorter, A., Allen, T.M., Zalipsky, S., Kamps, J.A., and Scherphof, G.L. (1999) Selective transfer of a lipophilic prodrug of 5-fluorodeoxyuridine from immunoliposomes to colon cancer cells. Biochim. Biophys. Acta 1420(1-2), 153-167. [Pg.1084]

Another useful technique which is closely related to fsREDOR is the band-selective transferred echo double resonance (BASE TEDOR) [102]. As shown in Fig. 6, the... [Pg.62]

Lee, K. J. et al. 2005. Large-area, selective transfer of microstructured silicon A printing-based approach to high-performance thin-film transistors supported on flexible substrates. Adv. Mater. 17 2332-2336. [Pg.444]

If it were possible to identify or quantitatively determine any element or compound by simple measurement no matter what its concentration or the complexity of the matrix, separation techniques would be of no value to the analytical chemist. Most procedures fall short of this ideal because of interference with the required measurement by other constituents of the sample. Many techniques for separating and concentrating the species of interest have thus been devised. Such techniques are aimed at exploiting differences in physico-chemical properties between the various components of a mixture. Volatility, solubility, charge, molecular size, shape and polarity are the most useful in this respect. A change of phase, as occurs during distillation, or the formation of a new phase, as in precipitation, can provide a simple means of isolating a desired component. Usually, however, more complex separation procedures are required for multi-component samples. Most depend on the selective transfer of materials between two immiscible phases. The most widely used techniques and the phase systems associated with them are summarized in Table 4.1. [Pg.48]

Selective transfer of material in microgram to gram quantities between two immiscible liquid phases separations based on solubility differences selectivity achieved by pH control and complexation. [Pg.49]

Solvent extraction, sometimes called liquid-liquid extraction, involves the selective transfer of a substance from one liquid phase to another. Usually, an aqueous solution of the sample is extracted with an immiscible organic solvent. For example, if an aqueous solution of iodine and sodium chloride is shaken with carbon tetrachloride, and the liquids allowed to separate, most of the iodine will be transferred to the carbon tetrachloride layer, whilst the sodium chloride will remain in the aqueous layer. The extraction of a solute in this manner is governed by the Nernstpartition or distribution law which states that at equilibrium, a given solute will always be distributed between two essentially immiscible liquids in the same proportions. Thus, for solute A distributing between an aqueous and an organic solvent,... [Pg.49]

Selective transfer of material in sub-microgram to milligram quantities between a solid sorbent and a liquid phase separations depend on different relative affinities for the two phases based on adsorption, size or charge selectivity achieved by pH control, solvent composition and surface chemistry of the sorbent. [Pg.70]

Requirements for the McLafferty rearrangement in a broad sense i) the atoms A, B, and D can be carbons or heteroatoms, ii) A and B must be connected by a double bond, hi) at least one y-hydrogen is available that iv) is selectively transferred to B via a six-membered transition state, v) causing alkene loss upon cleavage of the p-bond. [Pg.265]

Potentiometric detection is based on selective transfer of an ion in the solution into a lipophilic membrane phase, which generates a potential difference between the internal filling solution of the sensor and the sample solution. The electrode is generally placed at the outlet of the detector, and the membrane does present ion-selective characteristics. ... [Pg.324]

Scheme 10.1S. Dummy ligands selective transfer of the methyl (or alkyl, alkenyl, aryl) group in preference to transfer of the alkynyl group. Scheme 10.1S. Dummy ligands selective transfer of the methyl (or alkyl, alkenyl, aryl) group in preference to transfer of the alkynyl group.

See other pages where Selective transfer is mentioned: [Pg.138]    [Pg.16]    [Pg.292]    [Pg.112]    [Pg.204]    [Pg.1020]    [Pg.1020]    [Pg.697]    [Pg.1027]    [Pg.1126]    [Pg.198]    [Pg.79]    [Pg.277]    [Pg.500]    [Pg.559]    [Pg.561]    [Pg.500]    [Pg.635]    [Pg.639]    [Pg.402]    [Pg.310]    [Pg.279]    [Pg.237]    [Pg.769]    [Pg.352]    [Pg.415]    [Pg.456]    [Pg.1473]    [Pg.77]    [Pg.269]    [Pg.112]    [Pg.281]   
See also in sourсe #XX -- [ Pg.111 , Pg.112 ]

See also in sourсe #XX -- [ Pg.264 , Pg.269 ]




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Atom transfer reaction selection rules

Effect of interparticle mass transfer on catalytic selectivity

Electron transfer dissociation peptide selection

Electronic energy transfer mechanism selection rules

Energy transfer selection rules

Equipment selection heat transfer, figure

Equipment selection heat transfer, table

Face-selective hydride transfer

Hydrogen transfer selective reduction

Influence of External and Internal Mass Transfer on Selectivity

Method transfer testing laboratory selection

Non-Selective Polarization Transfer

Oligosaccharide synthesis by selective single-electron transfer

Oxygen selective transfer

Phase transfer catalyst asymmetric selection

Phase-transfer reactions, selective protection

Product selectivity mass transfer effect

Proton transfer facial selectivity

Selective Excitation and Energy Transfer

Selective Hartmann-Hahn coherence transfer

Selective Population Transfer (SPT)

Selective electron transfer quenching

Selective energy transfer model

Selective exclusion/transfer

Selective magnetization transfer

Selective polarization transfer

Selective population transfer

Selective-frequency polarization transfer

Selectivity and mass transfer

Selectivity mass transfer effect

Selectivity, phase-transfer benzylation

Site-Directed Mutagenesis in the Study of Substrate Selectivity and Electron Transfer

Spin selective population transfer

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