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Recognition, synthetic

Chang SK et al (1991) Hydrogen-bonding and molecular recognition - synthetic, complex-ation, and structural studies on barbiturate binding to an artificial receptor. J Am Chem Soc 113 7640-7645... [Pg.150]

Anion recognition synthetic receptors for anions and their application in sensors Snowden, T. S. Anslyn, E. V. Curr. Opin. Chem. Biol. 1999, 3, 740-746. [Pg.78]

Many complex systems have been spread on liquid interfaces for a variety of reasons. We begin this chapter with a discussion of the behavior of synthetic polymers at the liquid-air interface. Most of these systems are linear macromolecules however, rigid-rod polymers and more complex structures are of interest for potential optoelectronic applications. Biological macromolecules are spread at the liquid-vapor interface to fabricate sensors and other biomedical devices. In addition, the study of proteins at the air-water interface yields important information on enzymatic recognition, and membrane protein behavior. We touch on other biological systems, namely, phospholipids and cholesterol monolayers. These systems are so widely and routinely studied these days that they were also mentioned in some detail in Chapter IV. The closely related matter of bilayers and vesicles is also briefly addressed. [Pg.537]

The reaction of iodobenzene with acrylate is a good synthetic method for the cinnamate 17[7]. In the competitive reaction of acrylate with a mixture of 0-and /i-iodoanisoles (18 and 19), the o-methoxycinnamate 20 was obtained selectively owing to the molecular recognition by interlamellar montmorillonite ethylsilyldiphenylphosphine (L) as a heterogenized homogeneous catalyst used as a ligand[28]. [Pg.130]

There are three advantages to study molecular recognition on surfaces and interfaces (monolayers, films, membranes or soHds) (175) (/) rigid receptor sites can be designed (2) the synthetic chemistry may be simplified (J) the surface can be attached to transducers which makes analysis easier and may transform the molecular recognition interface to a chemical sensor. And, which is also a typical fact, this kind of molecular recognition involves outside directed interaction sites, ie, exo-receptor function (9) (see Fig. 5b). [Pg.190]

Another synthetic strategy is based on self-assembly driven by molecular recognition between complementary TT-donors and 7T-acceptors. Examples include the synthesis of catenanes and rotaxanes that can act as controUable molecular shuttles (6,236). The TT-donors in the shuttles are located in the dumb-beU shaped component of the rotaxane and the 7T-acceptors in the macrocycHc component, or vice versa. The shuttles may be switched by chemical, electrochemical, or photochemical means. [Pg.209]

The discovery of folic acid as a vitamin and the recognition of its versatile modes of action in biological systems focused early attention on simple synthetic pteridines with... [Pg.324]

Figure 8.15 Sequence-specific protein-DNA interactions provide a general recognition signal for operator regions in 434 bacteriophage, (a) In this complex between 434 repressor fragment and a synthetic DNA there are two glutamine residues (28 and 29) at the beginning of the recognition helix in the helix-turn-helix motif that provide such interactions with the first three base pairs of the operator region. Figure 8.15 Sequence-specific protein-DNA interactions provide a general recognition signal for operator regions in 434 bacteriophage, (a) In this complex between 434 repressor fragment and a synthetic DNA there are two glutamine residues (28 and 29) at the beginning of the recognition helix in the helix-turn-helix motif that provide such interactions with the first three base pairs of the operator region.
Given structure 1 as a target and the recognition that it contains the retron for the Diels-Alder transform, the application of that transform to 1 to generate synthetic precursor 2 is straightforward. The problem of synthesis of 1 is then reduced retrosynthetically to the simpler... [Pg.7]

Interdependence of redox and molecular recognition of natural and synthetic heterocycles 99ACR44. [Pg.224]

Macroheterocycles as synthetic receptors for steroids in molecular recognition 97CRV1567. [Pg.237]

Preorganization of DNA and improving nucleic acid recognition by synthetic oligonucleotides 97CRV1473. [Pg.263]

Progress in molecular recognition of functionalized calixarenes with hetero-atomic bridges as synthetic receptors 99MI43. [Pg.268]


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See also in sourсe #XX -- [ Pg.395 ]




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