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  • Radicals  (11)
  • Wiley-Blackwell  (11)
  • American Institute of Physics
  • Blackwell Publishing Ltd
  • Oxford University Press
  • 2000-2004  (11)
Collection
Publisher
  • Wiley-Blackwell  (11)
  • American Institute of Physics
  • Blackwell Publishing Ltd
  • Oxford University Press
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 2000 (2000), S. 1677-1683 
    ISSN: 1434-193X
    Keywords: Radicals ; Cyclizations ; Pyridinethione ; Tetrahydrofurans ; Asymmetric synthesis ; Thiazolethione ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---The trisubstituted functionalized tetrahydrofurans 10, 11, 16, 18, and 19 were photochemically prepared from 2,3-syn- and 2,3-anti-configuredN-(3-benzoyloxy-5-hexen-2-oxy)thiazole-2(3H)-thione anti-6, pyridinethiones 7, anti-8, and BrCCl3. The formation of tetrahydrofurans was achieved by an efficient and highly regioselective alkoxyl radical cyclization (5-exo-trig). The 2,3-anti substituted intermediates 9 and 12 cyclize stereoselectively whereas a 2,3-syn-configured O-radical affords both possible diastereomeric addition products in equal amounts. The cyclized tetrahydrofuryl methyl radicals were trapped with the bromine atom donor BrCCl3 to afford the bromomethyl-substituted cyclic ethers 10, 11, 18, and 19 in excellent yields. The utility of this reaction was stressed by conversion of one of the newly prepared tetrahydrofurans in a two-step synthesis into (+)-allo-muscarine (+)-20.Supporting information for this article is available on the WWW under //http://www.wiley-vch.de/contents/jc_2046/2000/99590_s.pdf or from the author.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 2000 (2000), S. 381-385 
    ISSN: 1434-193X
    Keywords: Enynes ; Macrocycles ; Coordination chemistry ; Crown compounds ; Radicals ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---The complex molecular structure and interesting activation mechanisms of naturally occurring enediynes have inspired the synthesis of a variety of simpler model systems to mimic their properties. While in most model compounds nucleophilic attack, isomerization or bioreduction are used to activate the unsaturated system for diradical cyclization, some attempts have been made to employ metal-ion coordination for this purpose. Significant enhancement of the thermal reactivity has been achieved by metal-ion induced conformational and electronic changes of suitably substituted enediynes, such as 1, 5, 6, 17 and 18. Enediyne activation by stoichiometric or catalytic formation of vinylidene complexes, such as 22, from terminal alkynes has also been investigated. This paper summarizes recent results pursuing the activation of enediyne diradical cyclization by metal ions.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 2000 (2000), S. 627-631 
    ISSN: 1434-193X
    Keywords: Complex nucleoside ; Antibiotics ; Radicals ; Zn-Cu couple ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---Homosinefungin 5, which can be considered as an analogue of S-adenosylmethionine (SAM) and of S-adenosylhomocysteine (SAH), has been synthesized by means of a sequence in which the key step was the addition of a radical, produced by the simple treatment of an iodide precursor with a zinc-copper couple, to suitably activated olefins.
    Additional Material: 1 Ill.
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  • 4
    ISSN: 1434-193X
    Keywords: Radicals ; Photochemistry ; Aliphatic ethers ; Hydrogen abstraction ; Urazolyl radical ; α-Alkoxy-alkyl radical ; Diones ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---The photoaddition of 4-methyl-1,2,4-triazoline-3,5-dione (4-MTAD) with a wide variety of acyclic, cyclic and crown aliphatic ethers has been investigated. Monochromatic (λ = 514.5 nm) or polychromatic (λ ≥ 310 nm) irradiations give identical mono-urazolyl ethers as reaction products. Unsymmetrical acyclic ethers afford a mixture of the two α and α′ mono-urazolyl ethers. In the case of 12-crown-4, mono and di-substituted products are obtained. ESR experiments and quantum calculations at the AM1 and 6-31G* levels were performed and a possible reaction mechanism is proposed in which the most probable photochemical process is the H-abstraction leading to a urazolyl radical.Supporting information for this article is available on the WWW under //http://www.wiley-vch.de/contents/jc_2046/2000/099269_s.pdf or from the author.
    Additional Material: 3 Ill.
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  • 5
    ISSN: 1434-193X
    Keywords: Photochemistry ; Radicals ; EPR spectroscopy ; Quantum mechanical calculations ; Silicon compounds ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -Trisilane 7 has been synthesized as a potential photochemical precursor of tetra-tert-butylsilatetrahedrane (5) and/or tetra-tert-butylsilacyclobutadiene (6). Astonishingly, only one Si,Si bond is broken upon irradiation of 7 and the silacyclobutenyl radical 9 can be identified as the reaction product. The structure of radical 9, which in the absence of oxygen is persistent even at room temperature, has been elucidated by comparison of its experimental and calculated ESR spectra.
    Additional Material: 2 Ill.
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  • 6
    ISSN: 1434-1948
    Keywords: Radicals ; Carbenium ions ; Clusters ; Cobalt ; Molybdenum ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complexed α-CF3 propargyl alcohols of the general formula [(M2L6){μ-η2,η2-RC≡CCH(CF3)(OH)}] were prepared with M2L6 = Co2(CO)6, R = CH3(CH2)4- (1), R = C6H5- (2); M2L6 = Co2(CO)5P(C6H5)3, R = CH3(CH2)4- (3a,b), R = C6H5- (4a,b); M2L6 = Co2(CO)4dppm, R = C6H5- (5); M2L6 = Co(CO)3MoCp(CO)2, R = CH3(CH2)4- (6a,b), R = C6H5- (7a,b). An X-ray molecular structure of the propargyl-alcohol complex [{Co2(CO)4dppm}{μ-η2,η2-C6H5C≡CCH(CF3)(OH)}] (5) was also determined. The related carbenium ions [(M2L6){μ-η2,η3-RC≡CCH(CF3)}][BF4] (8-12) were obtained from the parent propargyl alcohol complexes by direct protonation with HBF4· Et2O in diethyl ether. These carbenium ions were reduced further by Zn in CH2Cl2 to give the alkyne adducts [(M2L6){μ-η2,η2-RC≡CCH2(CF3)}] (13-17), as confirmed by the X-ray molecular structure of [(Co2(CO)4dppm){μ-η2,η2-C6H5C≡CCH2(CF3)}] (17). Treatment of the carbenium ion complex [{Co(CO)3MoCp(CO)2}{μ-η2,η3-CH3(CH2)4C≡CCH(CF3)}][BF4] (8) with NaSMe unexpectedly afforded the reduced alkyne adduct [{Co(CO)3MoCp(CO)2}{μ-η2,η2-CH3(CH2)4C≡CCH2(CF3)}] (13), along with the alkyne-thioether diastereomers {Co(CO)3MoCp(CO)2}{μ-η2,η2-CH3(CH2)4C≡CCH(CF3)[(SMe)}] (18a,b). Presumably, all the reduction reactions proceed primarily by the formation of the transient radical species, which are subsequently transformed into the reduced alkyne complexes by hydrogen abstraction from the solvent medium. Interestingly, in the case of the complexed alcohols [{Co2(CO)5P(C6H5)3}{μ-η2,η2-RC≡CCH(CF3)(OH)}] (3a,b) and (4a,b), the reduction process occurs in acidic medium in THF/CH2Cl2. An extensive study of the electronic and steric factors that influence the stability and reactivity of the carbenium ions were performed, which allowed us to explain the behavior of the related radical species in solution during the reduction process.
    Additional Material: 4 Ill.
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  • 7
    ISSN: 1434-1948
    Keywords: Palladium ; Dithiadiazole ; Radicals ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two new 1,2,3,5-dithiadiazoles, [4-(4′-C5H4N)CN2S2] (L1) and [4-(3′-C5H4N)CN2S2] (L2), with different pyridyl groups at the 4-position were prepared. As Lewis bases, the dithiadiazoles reacted with Lewis acids via their pyridyl groups to form acid-base adducts with retention of the five-membered dithiadiazole ring. Ligands L1 and L2 reacted with excess triethylborane to give L1BEt3 and L2BEt3 (1a and 1b) and with Mn(CO)5Br to give the fac-Mn(CO)3Br(L1)2 (2a) and fac-Mn(CO)3Br(L2)2 (2b) complexes. When reacted with Pd0 complexes, namely, Pd(PPh3)4 and a mixture of [Pd2(dba)3] and dppf, the dithiadiazoles underwent ring-opening reaction by reductive cleavage of the S-S bond of the dithiadiazole ring. The resulting formation of Pd-S bonds gave the corresponding trinuclear complexes [Pd3{μ-SNC(4′-C5H4N)NS-S,S′}2(PPh3)4] (3a), [Pd3{μ-SNC(3′-C5H4N)NS-S,S′}2(PPh3)4] (3b), and [Pd3{μ-SNC(4′-C5H4N)NS-S,S′}2(dppf)2] (4) [dba = dibenzylideneacetone, dppf = 1,1′-bis(diphenylphosphanyl)ferrocene]. Complexes 3a and 3b reacted with excess triethylborane to give the corresponding acid-base adducts [Pd3{μ-SNC(4′-C5H4NBEt3)NS-S,S′}2(PPh3)4] (5a) and [Pd3{μ-SNC(3′-C5H4NBEt3)NS-S,S′}2(PPh3)4] (5b.) Complex 3a reacted with Mn(CO)5Br to give {[Pd3{μ-SNC(4′-C5H4N)NS-S,S′}2(PPh3)4][MnBr(CO)3]}n (6). The structures of 3a, 5a, and 5b were established by X-ray crystallography.
    Additional Material: 3 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 2000 (2000), S. 447-454 
    ISSN: 1434-1948
    Keywords: Zinc ; Metalloporphyrins ; Porphyrins ; Cations ; Radicals ; ESR ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Zinc(II) complexes of substituted tetraphenylporphyrins, Zn[T(X-P)P], where X = H, p-F, p-Cl, m-Cl, p-CH3O, and m-CH3O, have been synthesized and characterized. Peripheral substitution shows marked changes in the chemical shifts of the phenyl proton resonances and E1/2 values of the redox couples in the anodic region while the UV/Vis spectra are unaffected. The monocation radicals of these complexes are generated by chemical oxidation with bromine. The ESR spectra reveal the formation of two types of radical species, Zn[T(X-P)P]+·Br- (species I) and Zn[T(X-P)(Brn-P)]+·Br- (species II): Species I at 298 K shows a spectrum, with well-resolved bromine hyperfine features, characteristic of a 2A2u electronic ground state while species II, except for the complex with X = m-CH3O, shows a featureless, isotropic resonance attributable to a 2A1u state. Zn[T(m-CH3O-P)(Brn-P)]+·Br-, on the other hand, exhibits nine resolved nitrogen hyperfine features corresponding to a 2A2u state. Variable temperature ESR spectra (77-298 K) indicate reduction in the bromine and nitrogen hyperfine coupling constants and an increase in the g value of species I from 2.0049 to 2.0060 with lowering temperature and suggest a labile electronic ground state for species I. The p-CH3O substituted complex exhibits an electronic transformation from 2A2u to 2A1u while the remaining complexes, including m-CH3O, show a transformation from 2A2u to an admixed 2A1u/2A2u state. The effect of substitution on the variable temperature ESR spectra are discussed.
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  • 9
    ISSN: 1434-1948
    Keywords: Manganese ; Radicals ; Cyclic dimer complexes ; Exchange coupling parameters ; Spin states ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Temperature-dependent paramagnetic susceptibility data for two cyclic dimer complexes of bis(hexafluoroacetylacetonato)manganese(II) with 5-tert-butyl-1,3-phenylenebis(N-tert-butylaminoxyl) and 4-(N-tert-butyl-N-oxyamino)pyridine have been analyzed to obtain two sets of two intramolecular exchange coupling parameters J1 and J2. A previous model, based on one of these interactions being much weaker than the other, could not be explicitly correlated to these actual exchange-coupling parameters. However, the energy levels of the low-lying spin states were found to be reproduced reasonably well by the approximate method.
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  • 10
    ISSN: 1434-193X
    Keywords: Photochemistry ; Furans ; Thiophenes ; Radicals ; Electron-poor olefins ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---Photochemical reactions of some haloheterocycles bearing electron-withdrawing groups 1a-d with electron-poor olefins 2a-c gave the addition products 3a-f and 3h-m in good yields. Other products obtained were the corresponding olefins 4a-k and the alkanes 3g. These reactions involve homolytic cleavage of the carbon-halogen bond to give the corresponding radical. The nature of these radicals has been studied. Ab initio calculations at the MP2/6-31G* level are supportive of the formation of σ radicals. These radicals are electrophilic and interact with the HOMOs of the electron-poor olefins.
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