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  • 1
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 1397-1402 
    ISSN: 0009-2940
    Schlagwort(e): Cyclobutane-1,3-diones ; Cyclobutane-1,3-dithiones ; Radical anions ; Diradical dianions ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 2,4-Bis(diphenylmethylene)-1,3-cyclobutanedione (1) is transformed into its sulphur analogues 2 and 3 with Lawesson's or Davy's reagent 5a,b. An X-ray structural analysis is performed on 3. The electrochemistry of these compounds is surveyed. The products of the electrochemical reduction exhibit ESR spectra, which could not be attributed to the radical anions 1-•, 2-•, and 3-•. Extensive semiempirical AM1/Cl calculations suggest the spectra to correspond to the diradical dianions. The experimental data are discussed in terms of the theoretical results.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 1485-1487 
    ISSN: 0009-2940
    Schlagwort(e): Thioketenes ; Flash-vacuum pyrolysis ; Diels-Alder reaction ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Flash-vacuum pyrolysis of 2,4-bis(dichloromethylene)-1,3-dithietane (1) at 820°C furnishes dichlorothioketene (2a) which may be trapped with cyclopentadiene (3) in a [4+2] cycloaddition. The constitution 4a of the product is confirmed by an X-ray structural analysis of the related cycloadduct 4b.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 1885-1885 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 123 (1990), S. 2065-2068 
    ISSN: 0009-2940
    Schlagwort(e): Benzo[c]thiophenes ; Oxidation ; Quinones ; Sulfines ; Diels-Alder reaction ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Unexpected Diels-Alder and Oxidation Reactions of Benzo[c]thiophenesThe oxidation of thiophenes by peracids to form thiophene S-oxides could not be carried out with benzo[c]thiophenes. With the sterically hindered compound 1a the quinones 2 and 3 were produced whereas the anisyl-substituted derivative 1b formed the sulfine 5. Significantly different behaviour of 1a and 1b was also observed for the Diels-Alder reaction with N-phenylmaleimide. The unexpected and unusual adduct 6 was the only product formed from 1a, with low yield though, whereas the normal Diels-Alder adduct was obtained from 1b.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    ISSN: 0009-2940
    Schlagwort(e): Cyclopropyl building blocks ; Strained compounds ; [4 + 2] Cycloaddition ; Regioselectivity ; Epoxides, regioselective cleavage of ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 1-Ethoxy- (8a) and 1-(trimethylsilyloxy)-1,3-pentadiene (8b) cycloadded to 2-chloro-2-cyclopropylideneacetate 6 to give low yields of endo/exo-9a and -9b, respectively. On the other hand, furans 5a-d added 6 (5b and 5d reacted regioselectively) to afford mixtures of the corresponding [4 + 2] cycloadducts endo-11a-d and exo-11a-d in good to high yields. 2-Methyl-5-(trimethylsilyloxy)furan (5e) yielded a mixture of the four cycloadducts endo/exo-11e and endo/exo-12e, which upon attempted purification on silica gel underwent facile hydrolysis to give bicyclic hemiacetals endo/exo-13 and 4-hydroxycyclo-2-hexen-1-ones endo/exo-14, respectively. Similarly endo/exo-11f, and endo/exo-12f, obtained from 2-methoxy-5-methylfuran (5f) and 6, upon hydrolysis in the presence of silica gel gave endo/exo-13 and endo/exo-14 respectively. The structures of endo-14 and exo-12f were established by X-ray crystallography. In the presence of florisil, the epoxides endo-and exo-16 were formed from trimethylsilyloxy-substituted cycloadducts endo/exo-11e. Selective reduction of the α-chlorocarboxylate functionality in the cycloadducts endo-11a-d,f with LiBH4, followed by base-catalyzed cyclization of the resulting chlorohydrins endo-21a-d, f yielded the corresponding epoxides endo-22a-d,f in 22-73% overall yield. Under identical conditions, the cycloadducts exo-11a-f could not be reduced to the corresponding chlorohydrins exo-21a-f. Regioselective reduction of the acetal epoxide endo-22f to the tertiary alcohol endo-23f was achieved with sodium dihydrobis(2-methoxyethoxy)aluminate (Red-Al®). On stirring with moist silica gel, the bicyclic acetals endo-22d,f and endo-23f cleanly hydrolysed to the highly substituted spiro[2.5]oct-6-en-5-ones endo-24d,f (26 and 24% overall yields, respectively, in four steps from 5d,f and 6) and endo-25f, respectively (23% overall yield in five steps from 5f and 6).
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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