Radical thiyl

The addition of aromatic and aUphatic thiols, RSH and ArSH, and a thioacetic acid to isoprene yields mainly the trans-l,4-adduct (56). The aromatic thiyl radicals, ArS , add almost entirely to the first carbon atom however, aUphatic thiyl radicals, RS, also add to the fourth C atom in significant amounts. 

The key to hexavalent chromium s mutagenicity and possible carcinogenicity is the abiHty of this oxidation state to penetrate the cell membrane. The Cr(VI) Species promotes DNA strand breaks and initiates DNA—DNA and DNA-protein cross-links both in cell cultures and in vivo (105,112,128—130). The mechanism of this genotoxic interaction may be the intercellular reduction of Cr(VI) in close proximity to the nuclear membrane. When in vitro reductions of hexavalent chromium are performed by glutathione, the formation of Cr(V) and glutathione thiyl radicals are observed, and these are beHeved to be responsible for the formation of the DNA cross-links (112). 

Thiyl radicals and their analogs in gas-phase syntheses and transformations of thiophenes 99ZOR11. 

The -elimination of a thiyl radical (RS ) terminated a remarkably productive tandem radical bicyclization in Parker s formal total syntheses of ( )-codeine and ( )-morphine (see Scheme 14).29 Subjection of aryl bromide 72 to the conditions indicated generates transient aryl radical 73, an intermediate which engages the substi-... 

Thiyl radicals are formed by transfer to thiols or by thermal or photochemical decomposition of disulfides (Scheme 3.84). 

Ring-opening provides a thiyl radical propagating species. Although the polymers have a double bond on the backbone there is little or no crosslinking (Scheme 4.34, Scheme 4.35). There is, however, evidence of reversible addition... 

Traditionally thiols or mercaptans are perhaps the most commonly used transfer agents in radical polymerization. They undergo facile reaction with propagating (and other) radicals with transfer of a hydrogen atom and form a saturated chain end and a thiyl radical (Scheme 6.6). Some typical transfer constants are presented in Table 6.2. The values of the transfer constants depend markedly on the particular monomer and can depend on reaction conditions.4"1 44... 

Thiols react more rapidly with nucleophilic radicals than with electrophilic radicals. They have very large Ctr with S and VAc, but near ideal transfer constants (C - 1.0) with acrylic monomers (Table 6.2). Aromatic thiols have higher C,r than aliphatic thiols but also give more retardation. This is a consequence of the poor reinitiation efficiency shown by the phenylthiyl radical. The substitution pattern of the alkanethiol appears to have only a small (<2-fokl) effect on the transfer constant. Studies on the reactions of small alkyl radicals with thiols indicate that the rate of the transfer reaction is accelerated in polar solvents and, in particular, water.5 Similar trends arc observed for transfer to 1 in S polymerization with Clr = 1.4 in benzene 3.6 in CUT and 6.1 in 5% aqueous CifiCN.1 In copolymerizations, the thiyl radicals react preferentially with electron-rich monomers (Section 3.4.3.2). 

Thiol-ene polymerization was first reported in 1938.220 In this process, a polymer chain is built up by a sequence of thiyl radical addition and chain transfer steps (Scheme 7.17). The thiol-ene process is unique amongst radical polymerizations in that, while it is a radical chain process, the rate of molecular weight increase is more typical of a step-growth polymerization. Polymers ideally consist of alternating residues derived from the diene and the dithiol. However, when dienes with high kp and relatively low A-, monomers (e.g. acrylates) are used, short sequences of units derived from the diene are sometimes formed. 

In this copolymerization, most termination is by chain transfer and most chains are initiated by transfer agent-derived radicals. The thiyl radicals generated from the transfer agent react faster with S than they do with acrylate esters (Scheme 7.20). 

Other side reactions that have been reported are cleavage of the carbon-nitrogen bond to form 24 and an aminyl radical 25 or scission of the tliiocarbonyl-sulfur bond to form a thiyl radical 26 and 27 (Scheme 9.I0). U 6 4 Thiocarbonyl-sulfur bond cleavage may be a preferred pathway in the case of primary dithioearbamates. 

The results were interpreted on the basis of a mechanism that starts with the photolytic formation of a radical cage consisting of an aryldiazenyl and and arylthiyl (Ar - S ) radical, followed by diffusion of both radicals out of the cage. Three reactions of the aryldiazenyl radical are assumed to occur bimolecular formation of the azoarene and N2, or of biphenyl and N2 (Scheme 8-37), the monomolecular dediazoniation (Scheme 8-38), and recombination with the thiyl radical accompanied by dediazoniation (Scheme 8-39). In addition, two radicals can react to form a di-phenyldisulfide (Scheme 8-40). 

The reaction of thiyl radicals with silicon hydrides (Reaction 8) is the key step of the so-called polariiy-reversal catalysis in the radical chain reduction. The reaction is strongly endothermic and reversible with alkyl-substituted silanes (Reaction 8). For example, the rate constants fcsH arid fcgiH for the couple triethylsilane/ 1-adamantanethiol are 3.2 x 10 and 5.2xlO M s respectively. 

In an analogous process, the reactions of unsubstituted and 2-substituted allyl phenyl sulfides with (TMSlsSiH give a facile entry to allyl fns(trimethylsilyl) silanes in high yields (Reaction 26). In this case, the addition of (TMSlsSi radical to the double bond is followed by the S-scission with ejection of a thiyl radical, thus affording the transposed double bond. Hydrogen abstraction from (TMSlsSiH by PhS radical completes the cycle of these chain reactions. ... 

The low reactivity of alkyl and/or phenyl substituted organosilanes in reduction processes can be ameliorated in the presence of a catalytic amount of alkanethiols. The reaction mechanism is reported in Scheme 5 and shows that alkyl radicals abstract hydrogen from thiols and the resulting thiyl radical abstracts hydrogen from the silane. This procedure, which was coined polarity-reversal catalysis, has been applied to dehalogenation, deoxygenation, and desulfurization reactions.For example, 1-bromoadamantane is quantitatively reduced with 2 equiv of triethylsilane in the presence of a catalytic amount of ferf-dodecanethiol. 

We suggest that the ejected thiyl radical undergoes a fast 1,2-migration of silyl group from silicon to sulfur (Reaction 85), affording a new silyl radical that either reacts with (TMSlsSiH (Reaction 86) which completes the reaction cycle, or replaces the (TMSlsSi radical in the above described reaction sequence. 

The method is not restricted to secondary aryl alcohols and very good results were also obtained for secondary diols [39], a- and S-hydroxyalkylphosphonates [40], 2-hydroxyalkyl sulfones [41], allylic alcohols [42], S-halo alcohols [43], aromatic chlorohydrins [44], functionalized y-hydroxy amides [45], 1,2-diarylethanols [46], and primary amines [47]. Recently, the synthetic potential of this method was expanded by application of an air-stable and recyclable racemization catalyst that is applicable to alcohol DKR at room temperature [48]. The catalyst type is not limited to organometallic ruthenium compounds. Recent report indicates that the in situ racemization of amines with thiyl radicals can also be combined with enzymatic acylation of amines [49]. It is clear that, in the future, other types of catalytic racemization processes will be used together with enzymatic processes. 

The degradation of tetrachloromethane by a strain of Pseudomonas sp. presents a number of exceptional features. Although was a major product from the metabolism of CCI4, a substantial part of the label was retained in nonvolatile water-soluble residues (Lewis and Crawford 1995). The nature of these was revealed by the isolation of adducts with cysteine and A,A -dimethylethylenediamine, when the intermediates that are formally equivalent to COClj and CSClj were trapped—presumably formed by reaction of the substrate with water and a thiol, respectively. Further examination of this strain classified as Pseudomonas stutzeri strain KC has illuminated novel details of the mechanism. The metabolite pyridine-2,6-dithiocarboxylic acid (Lee et al. 1999) plays a key role in the degradation. Its copper complex produces trichloromethyl and thiyl radicals, and thence the formation of CO2, CS2, and COS (Figure 7.64) (Lewis et al. 2001). 

The mechanoradical produced will react with the small amount of oxygen to form hydroperoxides these are subsequently utilised as radical generators in the second stage. The resulting hydroxyl radical (from hydroperoxide decomposition) abstracts a hydrogen from the substrate to form macroradical which, in turn, will react with more of the thiyl radical to form more bound antioxidant. The polymer bound antioxidant made in this way is very much more resistant to solvent leaching and volatilisation when compared to commercial additives (13). see Figure 2. 

It has been demonstrated that the MCR enzyme is active only if the metal center of coenzyme F430 is in the Ni1 form.1857 The natural substrate Me-CoM or simple methyl thioethers, however, do not react with Ni1 F430, which has lead to the proposal of a catalytic mechanism in which the addition of a thiyl radical to the S atom of the thioether giving a sulfuranyl radical intermediate is... 

The reaction of P-CAR with thiyl (RS ) and thiyl sulfonyl (RS()2 ) radicals have both been reported using pulse radiolysis (Everett et al. 1995, 1996). It was found that radical addition to P-CAR occurred and that p-CAR scavenges the thiyl radical, including that derived from glutathione, only via this mechanism, whereas it reacts with thiyl sulfonyl radicals by electron transfer as well. 

The radicals (14) formed may be trapped with, for example, (10) above. Simple alkyl thiyl radicals such as MeS have been detected as reaction intermediates they are highly reactive. Relatively stable oxygen-containing radicals are also known. Thus the phenoxy radical (15),... 

Thiyl radicals, RS-, may be obtained by hydrogen abstraction from RSH, and will then add readily to alkenes by a chain reaction analogous... 

Sulphenyl chlorides, e.g. C13CSC1, can also be used as sources of thiyl radicals, but here the addition is initiated by Cl- and the R S will thus become attached to the other carbon atom of the double bond ... 

Volume 251. Biothiols (Part A Monothiols and Dithiols, Protein Thiols, and Thiyl Radicals)... 

A review has been published on the methods of functionalization of tetrazoles for the period 2001 to mid 2005 <06RJOC469>. The search for new radical structures having both low selectivity and high reactivity toward the addition reaction onto alkenes has led to a new tetrazole-derived thiyl radical <06JOC9723>. 

H2O, EtOH, 90°C) can be overcome by using the Dess-Martin periodinane (DMP) (CH2CI2, 25°C) <06JOC8261>. The reaction probably proceeds via thiyl radical 50, which undergoes 1,5-homolytic radical cyclization followed by aromatization of radical 51 to give 2-arylthiazole 52. 

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