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Thiol functions

Silyl-derived protective groups are also used to mask the thiol function. A complete compilation is not given here since silyl derivatives are described in the section on alcohol protection. The formation and cleavage of silyl thioethers proceed analogously to simple alcohols. The Si—S bond is weaker than the Si—O bond, and therefore sulfur derivatives are more susceptible to hydrolysis. For the most part silyl ethers are rarely used to protect the thiol function because of their instability. Silyl ethers have been used for in situ protection of the — SH group during amide formation. ... [Pg.297]

Inspired by the elastin-based side-chain polymers, Lemieux et al. prepared elastin-based stimulus-responsive gold nanoparticles. To this end, they capped gold particles with a layer of a single repeat of thiol-functionalized VPGVG peptides (Fig. 17a). These nanoparticles showed LCST behavior, which was modulated by varying the pH of the solution [131]. [Pg.93]

A specific example where heterogeneous supports provide nanoparticle size-control is the immobilization of homogeneous silver nanoparticles on polystyrene [366]. This work was extended later to the development of a one-pot method for the size-selective precipitation of silver nanoparticles on PVP-protected thiol-functionalized silica. During the immobilization of very small silver nanoclusters both the size of the silver nanoclusters and the thickness of the silver layer on the support could be controlled directly by the reaction parameters applied (Fi re 16) [367]. [Pg.36]

Another example where antioxidant performance can be improved dramatically lies in the mechanochemlcally initiated addition of reactive antioxidants on rubbers (5.10) or unsaturated thermoplastics such as ABS (12). For example, using thiol antioxidants 2 and 3 as the reactive antioxidants, Kharasch-type addition of the thiol function to the polymer double bond takes place during melt processing to give bound antioxidant adduct (see Equation 1) the polymer becomes much more substantive under aggressive environments. [Pg.417]

Insertion of a C=0 or C=S group between hydroxy or amino groups and a thiol function in 1,2- or 1,3-positions leads to a five- or six-membered heterocycle ... [Pg.186]

In contrast with the role of cofactor B12 in methionine synthase (methyl group transfer to a thiol), functional Bi2 model complexes have provided a formidable challenge. Several oxime alkyl-cobalt (structural) B12 models when reacted with arene- and alkanethiolates lead only to... [Pg.105]

Silver and mercury salts have a long history of use as antibacterial agents.241-243 The use of mercurochrome ((40), Figure 18) as a topical disinfectant is now discouraged. Silver sulfadiazene (38) finds use for treatment of severe burns the polymeric material slowly releases the antibacterial Ag+ ion. Silver nitrate is still used in many countries to prevent ophthalmic disease in newborn children.244 The mechanism of action of Ag and Hg is through slow release of the active metal ion—inhibition of thiol function in bacterial cell walls gives a rationale for the specificity of bacteriocidal action. [Pg.830]

Etienne, M. Cortot, J. Walcarius, A. 2007. Preconcentration electroanalysis at surfactant-templated thiol-functionalized silica thin films. Electroanalysis 19 129-138. [Pg.311]

Figure 9. The plot of the elasic modulus (GO as a function of the extent of reaction shows more clearly that once the elastic modulus is detected, it increases at a rapid rate. In fact, G increases by more than three orders of magnitude for less than 20% change in conversion of the thiol functional groups. Figure 9. The plot of the elasic modulus (GO as a function of the extent of reaction shows more clearly that once the elastic modulus is detected, it increases at a rapid rate. In fact, G increases by more than three orders of magnitude for less than 20% change in conversion of the thiol functional groups.
Thiolysis of peptides Thiol-functionalized synthetic vesicles. Diastereoselectivities lower in vesicles than in micelles Moss et al., 1982c... [Pg.285]

Hydroxamate-, imidazole- and thiol-functionalized micelles and chymotrypsin. Rate comparisons... [Pg.286]

In the mitochondria, ONOO- can mediate damage to OXPHOS by nitrosylat-ing/oxidizing tyrosine or thiol functional groups, rendering catalytic inactivation of complex I [NADH ubiquinone oxidoreductase], complex II [succinate ubiquinone oxidoreductase] and complex V (FI, FO-ATPase), thereby impeding ETC/ OXPHOS... [Pg.362]

Acetyltransferases catalyze the acetylation of amino, hydroxyl, and thiol functional groups. Acetylation of hydroxy and thiol groups is comparatively rare and of much less importance in alkaloid metabolism than reactions with amino functional groups. The types of amines that are acetylated include arylamines (the major route of metabolism in many species), aliphatic amines, hydrazines, sulfonamides, and the a-amino group of cysteine conjugates. The purification, physical properties, and specificity of the N-acetyltransfereases have been reviewed (116-118). [Pg.355]

Similarly, Hg(n) binding to thiol-functionalized mesoporous silica for which effective access to all the binding sites (100% of SH groups com-plexed with Hg(n) was achieved in micelle-templated mesostructures with pore diameters larger than 2.0 nm, whereas incomplete filling was always observed with corresponding amorphous silica-based adsorbents.37... [Pg.39]

The conversion of acyl isothiocyanates 47 with sodium azide leads to thiol-functionalized tetrazole derivatives such as 48 (Scheme 9) <1995PJC1022>. The reaction of 48 with chloro acetonitrile leads to an intermediate 49 that reacts in... [Pg.357]

Protection against cell damage due to oxidative stress is provided, amongst others, by glutathione (GSH), a cellular tripeptide with a thiol function in a cysteine residue. GSH is deprotonated to GS, which is a scavenger for electrophilic compounds and is reduced to GS SG in defense of reactive oxygen species [28]. [Pg.211]

This approach was based on the use of a thiol functionalized resin (Scheme 4.1). [Pg.67]

Further, N-methyl dithiocarbamate (MDTC) (.9) and N-metylglycine (sarcosine) (10) were similarly incorporated into PVC matrices resulting in the derivatives usable to chelate forming and introduction of thiol-function as shown in following scheme. Of the two main purpose of modification of commercial polymers 1) improvement of original property of each polymer and 2) incorporation of new function into the polymeric materials, our studies would be served from the viewpoint of the latter as the fundamental design for PVC and PECH with specific functions. [Pg.48]


See other pages where Thiol functions is mentioned: [Pg.490]    [Pg.5]    [Pg.412]    [Pg.413]    [Pg.47]    [Pg.528]    [Pg.536]    [Pg.166]    [Pg.124]    [Pg.289]    [Pg.359]    [Pg.14]    [Pg.104]    [Pg.9]    [Pg.72]    [Pg.465]    [Pg.461]    [Pg.120]    [Pg.492]    [Pg.416]    [Pg.156]    [Pg.162]    [Pg.551]    [Pg.339]    [Pg.96]    [Pg.130]    [Pg.4]    [Pg.68]    [Pg.84]    [Pg.460]    [Pg.451]   
See also in sourсe #XX -- [ Pg.230 ]




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Functional groups thio/thiol

Functional thiol

Functional thiol

Olefins and Functional Derivatives in the Presence of Carboxylic Acids, Thiols, Amines or Hydrogen Chloride

Peptide cysteine thiol functionalities

Peptides with thiol donor functions

Thiol functional groups, surface

Thiol functionalized cross linker

Thiol-functionalized PAMAM

Thiol-functionalized gold nanopartides

Thiol-reactive functions

Thiols functional group

Thiols, antioxidant function

Thiols, functionalization

Thiols, functionalization

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