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61.
The polymer-bound quinone2 has been prepared and used in column form with organic solvents for the convenient preparation of other quinones. In contrast to the solution reaction hydrocyanation of this quinone by the Thiele-Meisenheimer reaction did not yield a useful proportion of polymer-bound dicyanohydroquinone but instead gave a mixture of products including much monocyanohydroquinone. Helferich and Bodenbender's 2,3-dicyanocyclohexan-1, 4-dione is in fact wholly the di-enol and is a likely intermediate in the hydrocyanation of benzoquinone, being oxidised by the latter to 2,3-dicyanocyclohex-2-ene-1, 4-dione which tautomerises to the observed product, 2,3-dicyanohydroquinone. A lower accessibility to polymer-bound reactants as compared with those in solution is implied by these results. 相似文献
62.
Hugues dOrchymont Maurice P. Goeldner Jean-Fran?ois Biellmann 《Tetrahedron letters》1982,23(16):1727-1730
Beside the Wittig rearrangement and the migration of the cyclooctyl radical to the para position, the title carbanion gives rise to an elimination in a syn process. 相似文献
63.
64.
Thomas A. Elwood Kenneth H. Dudley Joan M. Tesarek Peter F. Rogerson Maurice M. Bursey 《Journal of mass spectrometry : JMS》1970,3(7):841-861
Several alkylhydroxynaphthoquinones and chemically related cyclic compounds were subjected to mass spectrometric investigation. Fragmentation pathways were elucidated by use of metastable ions, relative intensities of normal ions and accurate mass measurement. In these series, differences in the spectra of 1,2- and 1,4-naphthoquinones are slight. Evidence for ring expansion in ions from furans is suggested. 相似文献
65.
The C5H5+ fragment ion bound in many EI spectra is determined not to be cyclopentadienyl cation by CID-MIKE spectrometry. 相似文献
66.
Maurice R. Kibler 《International journal of quantum chemistry》1975,9(3):403-420
The aim of this paper is to explore in detail the mathematical connection between the point-charge electrostatic model and the angular overlap model. More precisely, for any configuration nlx in any symmetry, the matrix elements, and therefore the energy levels, as given by the angular overlap model restricted to the antibonding effects λ (for any of the possible λ's), are deduced from an effective potential constructed according to the point-charge electrostatic model. This allows us to give a mathematical proof of the equivalence between the point-charge electrostatic model and the angular overlap model taking into account all the antibonding effects λ. Finally, the sum rules for the angular overlap model are examined in the light of the formulae connecting the two models considered. Numerical tables for obtaining the results as given by the angular overlap model restricted to any of the antibonding effects from those as given by the point-charge electrostatic model are listed for the configurations nlx with l = p, d, f and g. 相似文献
67.
68.
(+)-Parviflorine (), found in Lam. (Fumariaceae), is the first known glycosidic spirobenzylisoquinoline alkaloid. Its acid hydrolysis yields (+)-parfumine () and D-glucose. Klyne's rule indicates that is a β-D-glucoside. The absolute configuration shown in expressions is predominant among spirobenzylisoquinolines. A generalization has been drawn between plant source and the oxygenation pattern of ring C for the spirobenzylisoquinoline alkaloids. 相似文献
69.
70.
S. Asghari Ahmed Peter W. Hickmott Maurice W. Cooper Ian A. Stenhouse 《Magnetic resonance in chemistry : MRC》1980,14(4):296-299
The 220 MHz 1H NMR spectra of 6-hydroxy-7-methyl-6-phenyladamantane-2,4-dione, 6-hydroxy-5,7-dimethyl-6-phenyladamantane-2,4-dione, and 6-hydroxy-7,9-dimethyl-6-phenyladamantane-2,4-dione have been determined and complete proton assignments carried out with the aid of multiple irradiation. The stereochemistry of the C-6 and C-9 chiral centres have been determined and some of the factors affecting the magnitude of the geminal, vicinal and W coupling constants are discussed. 相似文献