Oxidative addition of trifluoromethanesulfonamide to cycloalkadienes

Reactions of trifluoromethanesulfonamide with cyclopentadiene, cyclohexa-1,3- and -1,4-dienes, cyclohepta-1,3,5-triene, and cycloocta-1,3-diene in the presence of t-BuOCl-NaI were studied. Trifluoromethanesulfonamide added at one double bond of cyclopentadiene and cyclohexa-1,3-diene in regio- and stereoselective fashion to give N-(5-iodocyclopent-2-en-1-yl)trifluoromethanesulfonamide and trans-N,N′-cyclohex-3-ene-1,2-diylbis(1,1,1-trifluoromethanesulfonamide), respectively. The reaction with cyclohexa-1,4-diene involved both isolated double bonds to produce N,N′-(2-chloro-5-iodocyclohexane-1,4-diyl)bis(1,1,1-trifluoromethanesulfonamide) which underwent halophilic reduction of the CHI group by the action of NaI and elimination of HCl, leading to N,N′-(cyclohex-2-ene-1,4-diyl)bis(1,1,1-trifluoromethanesulfonamide). Under analogous conditions, cyclohepta-1,3,5-triene was oxidized to benzaldehyde, while no reaction with trifluoromethanesulfonamide occurred.     

Oxidative DNA damage following photoexcitation of daunomycin: Direct role of oxygen

The chemistry of the photoactivation of daunomycin–DNA complexes is reported and the mechanism is elucidated. We quantitatively assessed the type of DNA damage, such as strand breaks, oxidized bases, and abasic sites, that arise using a plasmid relaxation assay coupled with DNA repair endonucleases. Photoexcitation of daunomycin leads to oxidative DNA damage in a dose- and irradiation time-dependent manner and guanine-specific oxidized purines are substantially produced under these conditions. Oxidative DNA base damage was also inhibited by argon degassing, indicating that guanine-specific damage arises from an oxygen-dependent mechanism. In addition, photoexcitation of daunomycin–DNA complexes leads to superoxide anion radical formation. From these studies of the actual product formed, we conclude that a charge transfer is a main driving force of the mechanism.     

Oxidative addition of N-aminophthalimide to cinnamic aldehyde phthaloylhydrazone

Russian Journal of Organic Chemistry -     

Oxidative addition of trifluoromethanesulfonamide to vinylcyclohexane and p-chlorostyrene

Trifluoromethanesulfonamide reacted with vinylcyclohexane in the system t-BuOCl-NaI to give a mixture of 2,6-dicyclohexyl-1,4-bis(trifluoromethylsulfonyl)piperazine and 2-iodo-1-cyclohexylethanol. Conformational behavior of the heterocyclization product was studied by dynamic NMR. The reaction of p-chlorostyrene with trifluoromethanesulfonamide under analogous conditions produced the corresponding bis-adduct, N-[2-(4-chlorophenyl)-2-(trifluoromethylsulfonylamino)ethyl]trifluoromethanesulfonamide and 1-(4-chlorophenyl)-2-iodoethanol. A probable reaction mechanism was proposed, which rationalizes difference in the behavior of the examined alkenes.     

Oxidative addition of asparagusic acid based disulfides to Pt

[Pt(PPh₃)₄] reacts smoothly and swiftly at room temperature with asparagusic acid and with selected amide and ester derivatives of this cyclic disulfide to afford Pt^II dithiolate chelates of the type cis-[Pt{CRR′(CH₂S)₂}(PPh₃)₂]. The crystal structures of three such products are reported.     

Oxidative addition of water to novel Ir(I) complexes stabilized by dimethyl sulfoxide ligands.

The oxidative addition of water to novel Ir(I) DMSO complexes is described. IrCl(DMSO)3 (1) is synthesized in 90% yield when treating a toluene slurry of [Ir2Cl2(COE)4] (COE = cyclooctene) with excess DMSO. Its dimer, [Ir2Cl2(DMSO)4] (2) is obtained in 95% yield starting from 1. The cationic complex [Ir(DMSO)4]PF6 (6) is prepared in situ from [Ir(COE)2(O=CMe2)2]PF6 (5). These complexes add water at room temperature, giving rise to the oxidative addition products syn-[(DMSO)2HIr(mu-OH)2(mu-Cl)IrH(DMSO)2] [IrCl2(DMSO)2] (3) and anti-[(DMSO)2(DMSO)HIr(mu-OH)2IrH(DMSO)2(DMSO)](PF6)2 (7), respectively. Reductive elimination in pyridine leads to quantitative isolation of mixed Ir(I) DMSO-pyridine complexes IrCl(py)(DMSO)2 (4) and [Ir(py)2(DMSO)2]PF6 (8), respectively. Compounds 1, 3, and 7 have been characterized by X-ray crystallography. 3 and 7 show dimeric structures with the hydroxo ligands bridging the iridium atoms and in 7 both O- and S-bonded DMSO ligands are present.     

Oxidative addition of water and aliphatic alcohols by IrCl(trialkylphosphine)(3)

Oxidative addition of aliphatic alcohols to (C(8)H(14))IrCl(PMe(3))(3) in benzene yields the cis-hydrido-alkoxo products mer-cis-HIr(OR)Cl(PMe(3))(3) (R = Me, Et, 1-pentyl, 2-propyl). The analogous hydroxo complex is prepared by oxidative addition of water in THF. The addition rate depends on the nature of the alcohol (methanol > 1-pentanol > 2-propanol and methanol > water). The reaction is retarded in polar media but accelerated by protic cosolvents. Anionic ligand redistribution involving chloride and alkoxide (or hydroxide) competes with the oxidative addition reaction. A detailed kinetic study suggests that the 16-electron IrCl(PMe(3))(3) is the species undergoing the oxidative addition, and mer-cis-HIr(OR)Cl(PMe(3))(3) is the kinetic product. The reaction proceeds by a single-step nucleophilic attack of the metal on the O-H proton. Pi-donation by chloride stabilizes the transition state and governs the stereochemical course of the reaction. Protic solvent aggregation in the transition state in an apolar medium is suggested. mer-cis-HIr(OH)Cl(PEt(3))(3), obtained by water addition to IrCl(PEt(3))(3), was crystallographically characterized, showing an unusual hydrophobic cage around the hydride ligand.     

Oxidative addition reaction of o-quinones to triphenylantimony: novel triphenylantimony catecholate complexes

New catecholate Sb(V) complexes triphenyl(3,6-di-tert-butylcatecholato)antimony(V) Ph₃Sb(3,6-DBCat) (1) and triphenyl(perchloroxanthrenecatecholato)antimony(V) Ph₃Sb(^OXCat_Cl) (2) were synthesized by the oxidative addition reaction of corresponding o-quinones (3,6-di-tert-butyl-o-benzoquinone and perchloroxanthrenequinone-2,3) with triphenylantimony. Catecholates 1 and 2 can alternatively be synthesized by reacting the appropriate thallium catecholate with triphenylantimony dichloride. The oxidative addition reaction of an equimolar ratio of 4,4′-di-(3-methyl-6-tert-butyl-o-benzoquinone) and triphenylantimony yielded 4-(2-methyl-5-tert-butyl-cyclohexadien-1,5-dion-3,4-yl)-(3-methyl-6-tert-butyl-catecholato)triphenylantimony(V) Ph₃Sb(Cat-Q) (3); in the case of a 1:2 molar ratio, complex 4,4′-di-[(3-methyl-6-tert-butyl-catecholato)triphenylantimony(V)] Ph₃Sb(Cat-Cat)SbPh₃ (4) resulted. Complexes 1-4 were characterized by IR- and ¹H NMR spectroscopy. Molecular structures of 1, 2 and 4 were determined by X-ray crystallography to be a distorted tetragonal-pyramidal.     

Oxidative addition of aryl halides: routes to mono- and dimetallic nickel amino-bis-phosphinimine complexes

Oxidative addition of an aryl-halide to Ni(COD)(2) in the presence of an equivalent of amino-bis-phosphinimine ligand affords complexes of the form [HN(CH(2)CH(2)N=PPh(3))(2)Ni-Ar][X] (Ar = C(6)H(4)F, C(6)H(5), X = Cl, Br) while the analogous reactions with 2 equivalents of Ni yield the amido-bridged complexes N(CH(2)CH(2)N=PPh(3))Ni(2)Br(3) and N(1,2-C(6)H(4)N=PPh(3))Ni(2)Br(3).     

Electrolyzed-reduced water protects against oxidative damage to DNA, RNA, and protein

The generation of reactive oxygen species is thought to cause extensive oxidative damage to various biomolecules such as DNA, RNA, and protein. In this study, the preventive, suppressive, and protective effects of in vitro supplementation with electrolyzed-reduced water on H₂O₂-induced DNA damage in human lymphocytes were examined using a comet assay. Pretreatment, cotreatment, and posttreatment with electrolyzed-reduced water enhanced human lymphocyte resistance to the DNA strand breaks induced by H₂O₂ in vitro. Moreover, electrolyzed-reduced water was much more effective than diethylpyrocarbonate-treated water in preventing total RNA degradation at 4 and 25°C. In addition, electrolyzed-reduced water completely prevented the oxidative cleavage of horseradish peroxidase, as determined using sodium dodecyl sulfate-polyacrylamide gels. Enhancement of the antioxidant activity of ascorbic acid dissolved in electrolyzed-reduced water was about threefold that of ascorbic acid dissolved in nonelectrolyzed deionized water, as measured by a xanthine-xanthine oxidase superoxide scavenging assay system, suggesting an inhibitory effect of electrolyzed-reduced water on the oxidation of ascorbic acid.     

Oxidative addition of Pd0 to Ar-SO2R bonds: heck-type reactions of sulfones

[reaction: see text] Phenyl vinyl sulfones and sulfoxides react with Pd(OAc)(2) to form styryl sulfoxides and sulfones according to the first Mizoroki-Heck reaction reported for these thio derivatives. Only sulfones are able to react by using catalytic amounts of Pd (up to 1 mol %) in the presence of Ag(2)CO(3). 1,2-Diphenylsulfonyl ethenes, alkynylphenyl sulfones, and other sulfones, less prone to act as acceptors in the Heck-type reactions, can transfer the aryl group to alkyl acrylates forming cinnamic esters.     

Oxidative addition of dihydrogen to the bimetallic sulfide catalysts: evidence by X-ray photoelectron spectroscopy

Reversible transformations Ni(IV)↔Ni(II) in alumina and Sibunit supported (Ni,Mo) sulfide catalysts were observed after in situ thermal treatment of catalysts in an X-ray photoelectron spectrometer chamber. The phenomenon is interpreted as a reductive elimination of occluded hydrogen under low pressure and high temperature, and oxidative addition of hydrogen after catalyst treatment with an (H₂+H₂S) mixture.     

Oxidative addition of allylic carbonates to palladium(0) complexes: reversibility and isomerization

The oxidative addition of a cyclic allylic carbonate to the palladium(0) complex generated from a [Pd(dba)2]+2 PPh3 mixture affords a cationic pi-allylpalladium(II) complex with the alkyl carbonate as the counter-anion. This reaction is reversible and proceeds with isomerization of the allylic carbonate at the allylic position. The equilibrium constant has been determined in DMF. The influence of the precursor of the palladium(0) is discussed.     

A high energy barrier to charge recombination in ionized water vapor

A quantitative kinetic theory has been developed to explain the results of experimental observation of the abnormally intense clustering of water molecules in the vapor phase in an ionizing radiation field at a moderate dose rate. The recombination is impeded because of the hydration of ion pairs and the formation of an abnormally high energy barrier (∼100 k _B T) in molecular clusters. The buildup of the clusters of water molecules stabilized in the electric field of ion pairs results in a dramatic enhancement of the effect of ionizing radiation on the electric properties of the vapor. The values of the coefficients to the rate equation of ionization-recombination equilibrium were calculated on the molecular level by computer simulation of the hydration of the H₃O⁺(H₂O) _n OH⁻ ion pair using the detailed model of intermolecular interactions.     

Oxidative addition of unsaturated acid esters to 1,3-dimethyluracil and pyrimidine nucleosides

When alkyl esters of acrylic and sorbic acids or acrolein diethylacetal are reacted with 1,3-dimethyluracil or 1--D-xylofuranosyluracil in the presence of Pd(OAc) ₂ , oxidative addition takes place at position 5 of the uracil fragment.Institute of Organic Chemistry, Ural Branch, Russian Academy of Sciences, 450054 Ufa. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 7, pp. 1616–1618, July, 1992.