ライフサイエンスコーパス: thioether

1 le hinge region of an IgG1, can convert to a thioether.

2 w shows a strong interaction with the Met160 thioether.

3 ng reaction on the previously introduced C-2 thioether.

4 duction of a quinone mediated by an appended thioether.

5 b(I)alamin and the corresponding glutathione thioether.

6 the propylsulfonate group, presumably as the thioether.

7 in the asymmetric sulfoxidation of prochiral thioethers.

8 functionalities such as alkenes, amines, and thioethers.

9 nthesize enantioenriched tertiary thiols and thioethers.

10 e scope of alkenes to ethyl vinyl ethers and thioethers.

11 strategy for the synthesis of unsymmetrical thioethers.

12 O bonds in aryl ethers and C-S bonds in aryl thioethers.

13 nctional-group tolerant manner using alkynyl thioethers.

14 formed dehydro amino acids to produce cyclic thioethers.

15 hways is involved in the production of these thioethers.

16 rene, acetone, benzene, cyclohexanone, and 4 thioethers.

17 -selective in the reaction of this and other thioethers.

18 The synthesis of 5- to 8-memebered cyclic thioethers 4 has been achieved through a simple two-step

19 0 kcal mol(-1)), the carbon-sulfur bond of a thioether (71-74 kcal mol(-1)), and the carbon-oxygen bo

20 A stereospecific thioether activation-elimination protocol was developed

21 ino-3-(4'-maleimidylphenyl)-4-methylcoumarin-thioether adducts on three cysteine residues of JP1 (101

22 um dispersion reductive lithiation of phenyl thioethers, alkyl chlorides, acrolein diethyl acetal, an

23 Fluorotelomer thioether amido sulfonate (10:2-FTSAS) and fluorotelomer

24 pathways of 4:2, 6:2, and 8:2 fluorotelomer thioether amido sulfonate (FtTAoS) were characterized by

25 d such a catalytically active species in the thioether amination process.

26 C(Et)Ti) covalently linked to a chromium bis(thioether)amine ethylene trimerization center (SNSCr) wa

27 ain fatty acyl-CoAs and the non-hydrolyzable thioether analog of palmitoyl-CoA markedly accelerated C

28 um) as well as by a nonhydrolyzable acyl-CoA thioether analog.

29 eine into Dha formed a stable cystathionine (thioether) analogue of the complement inhibitor compstat

30 such as thiophenol allowed rapid assembly of thioether analogues that were converted into the corresp

31 Thioether ancillary ligands have been identified that ca

32 hesized via consistent use of oligosaccharyl thioether and oligosaccharyl bromide as glycosylation do

33 -hour cyclical changes in the levels of both thioethers and parasitemia.

34 MTT assays showed only minor effects of the thioethers and their oxidized derivatives on the cellula

35 rtion of appropriate linkers, such as ether, thioether, and amino type, into the inner section of the

36 vide the desired products of esters, ethers, thioether, and tertiary sulfonamide with 43-93% yields.

37 l- and aryl halides, trifluoromethyl groups, thioethers, and aromatic heterocycles).

38 y analysis revealed that these new porphyrin thioethers are highly distorted, exhibiting conformation

39 r with the extremely high flexibility of the thioether "arms" decorating the channels, account for a

40 g product was shown to be a quaternary vinyl thioether, as determined by X-ray crystallography.

41 herapeutic antibody dosed in humans formed a thioether at this position at a rate of about 0.1%/day w

42 links, HCCS-DeltaM13 cyt c contains only one thioether attachment.

43 )ESE, (DMM)ESP, and (DMM)ESDP, which are N3S(thioether)-based ligands varied in the nature of a subst

44 heme iron and native methionine ligands, but thioether-based heme-coordinating (type II) inhibitors a

45 Here, a thioether-based inhibitor (3) of neuronal nitric oxide s

46 1 combines an asymmetric BODIPY reporter and thioether-based ligand receptor to provide high selectiv

47 This, in turn, facilitates an intermediate thioether bond between Cys-143 and Ile-142, the site of

48 The cofactor consists of a thioether bond between the gamma-sulfur of residue cyste

49 y with excess Cu(II) to efficiently form the thioether bond but not the Y272 radical.

50 lates the interchange thiol that facilitates thioether bond cleavage and enolacetone formation during

51 drophobic active-site architecture promoting thioether bond cleavage and enolacetone formation not se

52 olacetone formed from dithiol-mediated 2-KPC thioether bond cleavage.

53 Furthermore, we were able to show that thioether bond formation is specific toward hydrophobic

54 S-Ribosylhomocysteinase (LuxS) cleaves the thioether bond in S-ribosylhomocysteine (SRH) to produce

55 gy transfer signal between CPT and maleimide thioether bond is monitored to visualize the drug releas

56 The thioether bond was the optimal linkage type, and TT and

57 potent conjugates linked via a nonreducible thioether bond were not.

58 orate these Uaas, which only form a covalent thioether bond with cysteine when positioned in close pr

59 e, copper-dependent formation of a C228-Y272 thioether bond, and generation of the Y272 radical.

60 an antibody via either a stable disulfide or thioether bond, in aqueous buffer solutions containing a

61 y transition via breakage of the C10/Cys-494 thioether bond, opposite rotations of the A and D pyrrol

62 Like all sactipeptides, SKF contains a thioether bond, which links the cysteine residue Cys4 wi

63 e synthesis and structural analysis of novel thioether bond-linked cyclic NGR peptides.

64 e in therapeutic antibodies can convert to a thioether bond.

65 re connected by a reduction-labile maleimide thioether bond.

66 on reaction resulting in the cleavage of the thioether bond.

67 , whereas a 24 h soak revealed the C228-Y272 thioether bond.

68 XCH) sites that covalently ligate heme b via thioether bonds and are classified into different classe

69 cytochrome c synthase (HCCS), leading to two thioether bonds between heme and a conserved CXXCH motif

70 requires the covalent attachment of heme by thioether bonds between heme vinyl groups and a conserve

71 Catalysis of the thioether bonds between the apocytochromes c and heme b

72 nsducing membranes and forms stereo-specific thioether bonds between the vinyl groups of heme b (prot

73 ovalently attached hemes that are formed via thioether bonds between the vinyls of heme b and cystein

74 proposal that heme puckering induced by both thioether bonds facilitate release of holocytochrome c f

75 -4 approximately Cys(2) heme b-apocytochrome thioether bonds in c-type cytochromes.

76 , closing the macrocycles, are stabilized by thioether bonds, formed between cysteines and dehydrated

77 rophilic carbon atoms, sulfur to Calpha atom thioether bonds, or carbon-carbon bond formation.

78 peptide antibiotics that contain one or more thioether bonds.

79 he pendant double bonds to the corresponding thioether bonds.

80 sized peptides that contain a characteristic thioether bridge (sactionine bond) that is installed pos

81 ple [4Fe-4S] clusters, to form the requisite thioether bridge between a cysteine and the alpha-carbon

82 The thioether bridge between the diacyl and dipeptide units

83 es were designed and synthesized, in which a thioether bridge was incorporated between a cysteine sid

84 ered peptides by cyclizing gamma-MSH using a thioether bridge.

85 c that exceptionally bind haem via only one thioether bridge.

86 modified with one disulfide and one cysteine thioether bridged to the alpha-position of a methionine,

87 re provides an entry point into various aryl thioether building blocks of pharmaceutical interest.

88 enable rapid access to fluorinated poly(aryl thioethers), but also opens new avenues for the processi

89 ductive lithiation of alkyl and vinyl phenyl thioethers by aromatic radical anions is shown to be the

90 When pyrazolate ligands with thioether chelate arms are used in cyclic coinage metal

91 Using a series of phosphine-thioether chelating ligands featuring meta- or ortho-car

92 y-d-manno-octulosonic acid (KDO) terminus by thioether chemistry.

93 LigG catalyzed glutathione-dependent beta-S-thioether cleavage with beta-S-glutathionyl-alpha-veratr

94 exhibited no or significantly reduced beta-S-thioether-cleaving activity with the beta(S)-epimer, dem

95 um ion (stabilized in the form of a cationic thioether complex) is markedly dependent on the electron

96 platinum-sulfur interaction of platinum(II)-thioether complexes.

97 When thioether concentrations were subjected to a phase shift

98 in S-sulfhydrated residues by forming stable thioether conjugates.

99 haptenation ratios and greater efficacy than thioether conjugation to maleimide activated KLH (mKLH).

100 thyl)-l-homocysteine) is a non-proteinogenic thioether containing amino acid.

101 eptides characterized by the presence of the thioether-containing amino acids lanthionine and methyll

102 y the post-translational installation of the thioether-containing amino acids lanthionine and methyll

103 hey are characterized by the presence of the thioether-containing bisamino acids lanthionine and meth

104 xidation catalyst indicates the potential of thioether-containing materials for oxidant sensing.

105 Thioether-containing poly(para-phenylene-ethynylene) (PP

106 and recombinant antibodies studied in vivo, thioether conversion rates were faster for IgG1 antibodi

107 miting step, and that rate acceleration upon thioether coordination is correlated to a change from a

108 ile at pH 10.0 results in the formation of a thioether coupled to regeneration of the active MCRred1

109 nerate the lanthionine and methyllanthionine thioether cross-linked amino acids from which lanthipept

110 ound in some nucleic acids and proteins, and thioether cross-links found in peptide natural products.

111 modified peptides containing characteristic thioether cross-links imperative for bioactivity and sta

112 to the Dha and Dhb residues to generate the thioether cross-links lanthionine and methyllanthionine,

113 de antibiotics containing the characteristic thioether cross-links lanthionine and methyllanthionine.

114 The connectivities of the thioether cross-links of paenicidin A were solved using

115 It contains five cyclic thioether cross-links of varying sizes that are installe

116 After installation of the characteristic thioether cross-links, tailoring enzymes introduce addit

117 monstrated that geobacillin I contains seven thioether cross-links, two more than the five cross-link

118 nd methyllanthionine residues that result in thioether cross-links.

119 terized by lanthionine and methyllanthionine thioether cross-links.

120 translationally modified peptides containing thioether cross-links.

121 These natural products contain thioether crosslinks formed by a cysteine attack on dehy

122 xial ligand variants (M81A, M81H) and single thioether cyt c variants.

123 Among 4-thioether derivatives, a 4-ethylthio analogue 23 display

124 Esters with a chelating thioether derived from commercially available 2-(methylt

125 Weakening the Cu-S bond via a change to the thioether donor found in (DMM)ESP leads to the initial f

126 ize a cupric superoxide complex possessing a thioether donor have resulted in the formation of an end

127 have one or two phosphine arms replaced with thioether donors.

128 The thioether effect also enables short reaction times under

129 , illustrating the intrinsic weakness of the thioether-ferric heme linkage.

130 be integrated into the target unsymmetrical thioether final products.

131 the development of four potent and selective thioether fluoroketone inhibitors as well as a thioether

132 ous state, reflecting the higher affinity of thioethers for ferrous heme than for ferric heme.

133 es, we discuss potential applications of the thioethers for the redispersion of metals on a catalyst

134 nts for both base-catalyzed racemization and thioether formation at the hinge disulfide.

135 or Xa cleavage site, indicating that correct thioether formation has occurred.

136 chanistic studies showed that base-catalyzed thioether formation through the light chain dehydrogenat

137 rs adjacent to the two heme vinyl groups for thioether formation; and (iii) to aid in release of the

138 Here we report that a thioether forms at the same position on antibodies in vi

139 thod has been developed for the synthesis of thioethers from carboxylates and thiols.

140 Using the thioether functional group inherent to this polymerizati

141 Sulfur atoms are present as thiol and thioether functional groups in amino acids, coenzymes, c

142 which enables the synthesis of well-defined thioether-functional poly(ethylene glycol).

143 prises the disulfide, diselenide, thiol, and thioether functionalities.

144 f the materials is achieved by the different thioether functionalization of the ligands L(SNf), L(SPh

145 amolecular assemblies are formed with Ag(+), thioether functionalized bis(pirazolyl)methane ligands a

146 The complexation of a preorganized thioether-functionalized bis(pyrazolyl)methane ligand (L

147 s, we were able to postulate a mechanism for thioether generation which is in agreement with that of

148 ucleic acid or protein targets with a methyl thioether group (-SCH(3)).

149 (2))(n)- spacers separating the coordinating thioether group from the strongly electron withdrawing p

150 However, introduction of a hydrophilic thioether group in the 6-position (15a-c, 15e-g) reduced

151 framework (PAF) densely functionalized with thioether groups for selective capture and concentration

152 th a well-defined cage structure and pendant thioether groups pointing inside the cavity are essentia

153 c Ag(+)-selective ionophores with one or two thioether groups were investigated.

154 ding alkenes bearing nitrile, sec-amine, and thioether groups.

155 on of high-performance fluorinated poly(aryl thioethers) has received little attention compared to th

156 tacts play a crucial role in stabilizing the thioether-heme coordination.

157 Contrary to what has been widely thought, thioether-heme ligation was found not to increase inhibi

158 room temperature to give a diversity of new thioether (hetera)cyclophanes in high yield.

159 a spatial scanning approach of a 10-membered thioether-heterocycle ring incorporated into a chimeric

160 onjugated seven-membered ring systems with a thioether in the macrocycle.

161 knowledge, the first crystal structure of a thioether inhibitor complexed to any heme enzyme.

162 these neuronal nitric oxide synthase (nNOS)-thioether inhibitor complexes in both crystal and soluti

163 We found that some thioether inhibitors switch from high to low spin at low

164 However, among the few thioether inhibitors that showed Fe-S thioether interact

165 ioether tail have been shown to form an Fe-S thioether interaction as evidenced by continuous electro

166 he few thioether inhibitors that showed Fe-S thioether interaction in crystal structures, variations

167 Even so, the Fe-S thioether interaction was found to be far less important

168 e keto-1,2,4-oxadiazole functionality with a thioether is a novel structure, and it will be used as a

169 loss of activity is abrogated when the M109 thioether is absent.

170 isulfides for the synthesis of quinonyl aryl thioethers is described.

171 The metabolic origin of the thioethers is not known, but results suggest that interp

172 ioether fluoroketone inhibitors as well as a thioether keto-1,2,4-oxadiazole inhibitor for GVIA iPLA2

173 otic enzyme responsible for the synthesis of thioether (lanthionine) cross-links within nascent polyp

174 The heme-thioether ligand interaction often occurs between heme i

175 ent of the cysteine(thiolate) with a neutral thioether ligand, Met (104).

176 lator composed of hemilabile phosphine alkyl thioether ligands (P,S) chelated to a Pt(II) center.

177 enes can occur under electronic control with thioether ligands even when this necessarily involves re

178 on geometries and progressively weaker axial thioether ligation across the series.

179 monomeric, superoxide product possessing a S(thioether) ligation, [((DMA)N3S)Cu(II)(O2(*-))](+) (2(S)

180 tuzumab linked to DM1 through a nonreducible thioether linkage (SMCC), displayed superior activity co

181 tide substrates containing a nonhydrolyzable thioether linkage as well as by site-directed mutagenesi

182 The thioether linkage between chromophore and protein is sub

183 /16 bond modulates formation of a reversible thioether linkage between Cys499 and C10 of the chromoph

184 OX) is covalently linked to the protein by a thioether linkage between its 8alpha-methyl group and Cy

185 teinase (LuxS) catalyzes the cleavage of the thioether linkage in S-ribosylhomocysteine (SRH) to prod

186 onally we demonstrate that generation of the thioether linkage is leader-peptide-dependent, suggestin

187 The thioether linkage produced by the reaction of oNQM and a

188 as a function of linker, determined that the thioether linkage provided sustained release of peptide

189 ated at various BEL concentrations to form a thioether linkage to a BEL keto acid hydrolysis product.

190 ore and, in certain cases, the breakage of a thioether linkage to a conserved cysteine residue in the

191 the reaction pathways diverge, the loss of a thioether linkage to a conserved cysteine residue occurs

192 ubfamily of CBCRs proceeds via a photolabile thioether linkage to a second cysteine fully conserved i

193 old, with the active-site cysteine forming a thioether linkage to the suicide substrate.

194 The final step, the formation of the thioether linkage with the protein, occurs with a lifeti

195 e three disulfide bridges is replaced with a thioether linkage, and evaluate the biological propertie

196 tached at the 6''-position of KANB through a thioether linkage, exhibited good antibacterial and anti

197 llows from (i) a sterically more constrained thioether linkage, leaving less mobility for ring A than

198 oparticles utilizing either a disulfide or a thioether linkage.

199 the light-dependent stability of the second thioether linkage.

200 Aqueous oxidation of the side-chain thioether linkages in these polymers to sulfone groups r

201 hycocyanobilin via two stable cysteine-based thioether linkages within the cGMP phosphodiesterase/ade

202 d with precisely positioned, multiresponsive thioether linkages.

203 hat typically harbor multiple intramolecular thioether linkages.

204 up to four ubiquitins, through disulfide and thioether linkages.

205 tion and stereoselective formation of beta-S-thioether linkages.

206 at are attached to specific Cys residues via thioether linkages.

207 g dehydro amino acids with cysteines to form thioether linkages.

208 wth in mice, however only treatment with the thioether linked vaccine construct resulted in enhanced

209 Immunization with either disulfide or thioether linked vaccine constructs effectively inhibite

210 eptide epitope (NWFDITNAibLWRR-NH(2)), and a thioether-linked peptide (NWFCITOWLWKKKK-NH(2)) to resol

211 The thioether-linked peptide is the first reported structure

212 the A-B methine bridge to generate a double thioether-linked phycoviolobilin-type chromophore.

213 t DM1 conjugated to trastuzumab via a stable thioether linker, has shown clinical activity in single-

214 DM1, a potent antimicrotubule agent, via the thioether linker, N-succinimidyl-4-(N-maleimidomethyl)cy

215 izing agents) conjugates using disulfide and thioether linkers.

216 with thiol groups on the surface, producing thioether links between the substrate and the surface.

217 In addition to the two cysteine thioether links to the porphyrin typical of c-type hemes

218 k bonds are azobisdialkylnitrile (weakest) < thioether < benzylphenyl ether.

219 The adverse effects of HQ and its thioether metabolites are in part a consequence of their

220 H2S-yielding reactions but also yields novel thioether metabolites, thus increasing the complexity of

221 MCR uses the methyl thioether methyl-coenzyme M (CH3-S-CH2CH2-SO3(-), Me-S-C

222 cyclic rings with concomitant intramolecular thioether migration.

223 mimetics in which isoxazole rings linked by thioethers mimic the alternating sites of carbonyls in t

224 edge XAS of WT and M121SeM azurin and a CuII-thioether model complex shows that the 38% S character i

225 Thioether modifications were also found at this position

226 Intriguingly, the thioether moieties of MTEGE can be selectively oxidized

227 ds were prepared by modifying the peripheral thioether moiety with naphthyl, methoxy, m-Me, p-Me and

228 describe a novel epoxide monomer with methyl-thioether moiety, 2-(methylthio)ethyl glycidyl ether (MT

229 here the alpha-alkoxy group is gauche to the thioether moiety.

230 tom of the carborane cage is attached to the thioether moiety.

231 ceed those of either polystyrene or the poly(thioether) network homopolymers alone.

232 phases dispersed throughout elastomeric poly(thioether) networks.

233 the cleavage of the C-S bond in alkyl phenyl thioethers on the lithium surface is dependent on the si

234 conditions: C-S lyase reaction using either thioether or sulfoxide as a substrate in the presence or

235 hemoselective manner to produce either vinyl thioethers or primary allylic thioesters in good yields.

236 by the reductive lithiation of alkyl phenyl thioethers or, usually less conveniently, alkyl halides

237 Amino acids containing a thiol, a thioether, or an extra amine group such as arginine, cys

238 Acylating the amino series, oxidizing the thioether, or replacing the ether oxygen with carbon sig

239 The reductive lithiation of phenyl thioethers, or alkyl chlorides, by either preformed arom

240 ere discovered and found to be connected via thioethers originating from disulfides at locations that

241 rnesal and cysteine by a membrane-associated thioether oxidase called farnesylcysteine lyase.

242 vestigate neighboring amide participation in thioether oxidation, which may be relevant to brain oxid

243 d Ni(II) complexes formed from two phosphino thioether (P,S) chelating ligands has been synthesized a

244 on, was functionalized with a phosphinoalkyl thioether (P,S) hemilabile moiety and incorporated into

245 Kinetic data suggest thioether-Pd-catalyzed reactions can be as much as 800x

246 sly, we reported the development of a cyclic thioether peptide with low micromolar inhibitory activit

247 ligands with bifunctional ether-phosphine or thioether-phosphine substituents at the 5 and 15 positio

248 s, amines, acids, alcohols, alkanes, ethers, thioethers, polymers, sugars) on five different substrat

249 (LK) represents a poorly understood class of thioethers present in mammalian CNS.

250 to MCRred1 by thiols involves formation of a thioether product.

251 eukaryotic cells catalyzes the formation of thioether products similar to glutathione S-transferase.

252 This reactivity allows for unwanted thioether products to be converted to the desired nitrob

253 rene adducts and nucleophilic capture benzyl thioether products.

254 involves a Suzuki coupling using tert-butyl thioether protecting groups.

255 naphthofluorescein chromophore and employs a thioether-rich metal-binding unit.

256 rromethene (BODIPY) chromophore coupled to a thioether-rich receptor, has a picomolar affinity for Cu

257 mprise a Gd(3+)-DO3A core coupled to various thioether-rich receptors for copper-induced relaxivity s

258 In particular, the rates of thioether ring formation are drastically reduced in Proc

259 a sulfur atom from the second thiolate as a thioether (RSR').

260 to imidazole nitrogens of H242, H244 and the thioether S of M314) and CuH (ligated to imidazole nitro

261 ecombinant Met(E11) mutants revealed similar thioether side chain orientations.

262 epimerization at C5, installation of the C2-thioether side chain, and C2/3 desaturation.

263 bapenam substrate must bear a CoA-derived C2-thioether side chain, implying the activity of a previou

264 n neoglycopeptides characterized by a simple thioether spacer.

265 ecyl radicals lead to the formation of a new thioether species R-S-R.

266 in an "off-on" fashion by a highly selective thioether spirocyclic nonfluorescent structure that open

267 t-translational modifications, including the thioether structures lanthionine and methyllanthionine.

268 The tolerance for nonhydrophilic thioether substituents in the 6-position opens up the po

269 n as a result of the selective conversion of thioether substituents into sulfoxides and sulfones.

270 Product analysis shows that the oxidation of thioether substrates gives sulfoxide product, consistent

271 The use of cyclopropyl and thioether substrates support the radical formation of al

272 n oxygen-atom transfer (OAT) reactivity with thioether substrates.

273 ng a stabilizing dendrimer based on benzylic thioether subunits.

274 mployed for coupling with various ethers and thioethers such as tetrahydrofuran, tetrahydropyran, 1,4

275 rength of noncovalent interactions between a thioether sulfur atom and various pi systems in designed

276 ne)methyl]phenol coordinates Hg(II) with two thioether sulfur atoms, two amino nitrogen atoms, and a

277 changes in the alkyl groups attached to the thioether sulfur caused drastic changes in the binding c

278 ioxygen reactivity includes the influence of thioether sulfur ligation, as it concerns the formation,

279 interactions between the alkyl group in the thioether tail and surrounding protein.

280 ogue nitric oxide synthase inhibitors with a thioether tail have been shown to form an Fe-S thioether

281 cularly with nearby cysteines to form cyclic thioethers termed lanthionines and methyllanthionines.

282 For ether and thioether-terminated layers, scission of C-O or C-S bond

283 and LigF) are beta-S-glutathionyl-alpha-keto-thioethers that are degraded by a beta-S-thioetherase (L

284 se, especially in view of the amenability of thioethers to be labeled with carbon-11 or fluorine-18 t

285 HCCS efficiently attaches heme via two thioethers to CXXCH of mitochondrial but not bacterial c

286 de intermolecular insertion of nitrogen into thioethers to form sulfimides.

287 st and TMSF byproducts.Fluorinated poly(aryl thioethers), unlike their poly(aryl ethers) counterparts

288 a dead-end product (a 4-methylcoumarin-3-yl thioether) upon photolysis.

289 o been used to prepare heteroaryl ethers and thioethers using phenol and thiophenol nucleophiles.

290 lyzed the coupling of azoles with ethers and thioethers via alpha-C(sp(3))-H activation.

291 hly efficient route to fluorinated poly(aryl thioethers) via an organocatalyzed nucleophilic aromatic

292 hly efficient route to fluorinated poly(aryl thioethers) via an organocatalyzed nucleophilic aromatic

293 A series of highly substituted porphyrin thioethers was synthesized from 2,3,7,8,12,13,17,18-octa

294 roups (nitro, cyano, halo, alkyl, amido, and thioether) was tolerated, and the route provided access

295 No thioethers were detected in in vitro cultures of Plasmod

296 Treatment of the resulting thioether with MSH results in regeneration of dehydroala

297 n the sulfoxidation of p-methylbenzyl methyl thioether with preference for the (S)-sulfoxide, the evo

298 The amination of thioethers with a chiral N-mesyloxycarbamate was achieve

299 des via acid-mediated coupling of thiols and thioethers with diaryliodonium salts is reported.

300 ofurazan (7-nitro-1,2,3-benzoxadiazole, NBD) thioethers with H2S resulted in thiol extrusion and form