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  • Inorganic Chemistry  (1,459)
  • Life and Medical Sciences  (1,183)
  • Wiley-Blackwell  (2,642)
  • 1980-1984  (2,642)
  • 1983  (1,399)
  • 1980  (1,243)
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  • Wiley-Blackwell  (2,642)
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  • 1980-1984  (2,642)
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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 800-805 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2,2-Disubstituted 1,3-Dithianes from β-Dicarbonyl Compounds1,3-Dicarbonyl compounds 2 can be condensed with 1,3-propanedithiol (1) to yield 2,2-disubstituted 1,3-dithianes 3 which are remarkably stable in contrast to analogous open-chain thioacetals 6. Compounds with alkoxycarbonyl functions are easily hydrolysed to the corresponding carboxylic acids 11 which by further esterification with alkanols 12 yield estermodified 1,3-dithianes 3. All new compounds are characterized by 13C NMR spectroscopy.
    Additional Material: 3 Tab.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 806-807 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Perchloro-2-methylene-2H-pyranThe synthesis of the title compound 4 is described. 4 is thermally and chemically very stable.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 808-810 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Anchimerically Enhanced Homolyses, V. Fluoride Ion Catalysed Rearrangements of Benzyl 9-(Trimethylgermyl)-9-fluorenyl EtherThe thermal rearrangement (homolysis) of the germanium compound 1d into 4d is considerably slower than that of the analogous Si compound 1c. Thus, a correlation is suggested between the velocity of the rearrangement and the strength of the new bond to oxygen. The rearrangement 1d→4d is also induced by fluoride ions at room temperature.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980) 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 116 (1983), S. 55-65 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Cycloaddition Reactions of Heterocumulenes, XXVI. Cycloadducts from Aryl Isothiocyanates and 2,2-Disubstituted EnaminesAryl isothiocyanates 1 react with enamines 2 to give two types of 2:1 cycloadducts. Below 50°C, 1a - g and 2 give rise to 6-imino-1,3-thiazine-2-thiones 5, the constitutions of which are proved by an X-ray analysis of 5c. Above 50°C or starting from 4-nitrophenyl isothiocyanate (1h),2,4-dithiouracils 6 are formed. 1:1 cycloadducts of the reactants are detected spectroscopically; on workup, they hydrolyze to give 2-formylthiopropionanilides 9.
    Notes: Arylisothiocyanate 1 und Enamine 2 reagieren zu zwei Typen von 2:1-Cycloaddukten. Unterhalb von 50°C entstehen aus 1a - g und 2 6-Imino-1,3-thiazin-2-thione 5, deren Konstitution durch die Röntgenstrukturanalyse von 5c bewiesen wurde. Oberhalb 50°C oder aus 4-Nitrophenylisothio-cyanat (1h) bilden sich 2,4-Dithiouracile 6. 1:1-Cycloaddukte der Reaktanten lassen sich spektroskopisch nachweisen; bei der Aufarbeitung hydrolysieren sie zu 2-Formylthiopropionaniliden 9.
    Additional Material: 3 Tab.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 116 (1983), S. 544-548 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Crystal and Molecular Structure of the Anthraquinonophane [2.0.0](1,4)Benzeno(1,8)anthraquinono(1,4)benzenophaneBoth phenylene rings in the [5.2]paracyclophane subunit of the anthraquinonophane [2.0.0](1,4)benzeno(1,8)anthraquinono(1,4)benzenophane (1) are tilted by 37.6°. They show a boat-like deformation. The carbonyl group pointing towards the interior of the molecule interacts with the paracyclophane system. From this a strong boat-like deformation of the quinone ring of the anthraquinone moiety results.
    Notes: Die beiden Phenylenringe in der [5.2]Paracyclophan-Untereinheit des [2.0.0](1,4)Benzeno(1,8)-anthrachinono(1,4)benzenophans (1) sind um 37.6° gegeneinander geneigt und wannenförmig deformiert. Die Wechselwirkungen der ins Molekülinnere zeigenden Carbonylgruppe mit dem Paracyclophan-System verursachen eine starke wannenförmige Deformation des Chinonringes in der Anthrachinon-Einheit.
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  • 7
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Four- and Five-membered Phosphorus Heterocycles, 55. 1,2,4-Diazaphospholo-[1,2,3]diazaphospholes - Preparation by Phosphaalkene + Nitrilimine Cycloaddition, Decomposition by Nitrile Elimination, and Structural Comparison of Addend and Adduct2,5-Dimethyl-1,2,3-diazaphosphole (1a) reacts with N-Phenylbenzohydrazonoyl chloride (6a) and a base in a sequence of nitrilimine cycloaddition, benzonitrile elimination, and another cycloaddition to give in the second step the 4-anilino derivative 7 of 1a, in the first and third step the 7a-unsubstituted and 7a-anilino-substituted title compound, 3a and 8, respectively. - As shown by the molecular structures, determined by X-ray analysis, there is a 6 π delocalization in 7 which is lost in 8 with remarkably little geometrical change at the phosphorus. - Other nitrilimines add to 1a in the same direction, that is with PC- and CN-bond formation.
    Notes: 2,5-Dimethyl-1,2,3-diazaphosphol (1a) reagiert mit N-Phenylbenzohydrazonoylchlorid (6a) und einer Base in einer Folge von Nitrilimin-Cycloaddition, Benzonitril-Eliminierung und neuerlicher Cycloaddition. In der zweiten Stufe bilden sich dabei das 4-Anilinoderivat 7 von 1a, in der ersten und dritten Stufe entstehen die 7a-unsubstituierte und 7a-anilinosubstituierte Titelverbindung, 3a bzw. 8. - Die röntgenographisch bestimmten Molekülstrukturen zeigen für den Übergang von 7 in 8 die Aufhebung einer 6 π-Delokalisierung bei nur geringen geometrischen Veränderungen am Phosphor. - Auch andere Nitrilimine addieren sich an 1a in gleicher Richtung, also unter PC- und CN-Verknüpfung.
    Additional Material: 6 Tab.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 919-933 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Thiono and Dithio Esters, XXII. α,β-Unsaturated Thiono and Dithio Estersα,β-Unsaturated thiono and dithio esters such as O-ethyl thiocinnamate (3), methyl dithiocinnamate (7), O-ethyl thiocrotonate (17), and O,O-diethyl dithiofumarate (28) have been prepared by thiolysis between 20 and -75°C from the corresponding O- or S-alkylated tertiary amides or thioamides. They tend to dimerize in part by [4 + 2] cycloadditions. Methyl dithiocrotonate (24) could only be isolated as the endo-dimer 25.
    Notes: α,β-Ungesättigte Thion- und Dithioester wie Thiozimtsäure-O-ethylester (3), Dithiozimtsäure-methylester (7), Thiocrotonsäure-O-ethylester (17) und Dithiofumarsäure-O,O-diethylester (28) sind durch Thiolyse aus den entsprechenden O- oder S-alkylierten tertiären Amiden oder Thio-amiden bei Temperaturen von 20 bis -75°C zugänglich. Sie dimerisieren zum Teil in [4 + 2]-Cycloadditionen. Dithiocrotonsäure-methylester (24) ist nur als endo-Dimeres 25 erhältlich.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 875-901 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Thermolysis of Compounds with a Geometrically Fixed Vinyloxirane Unit: Stereospecific Synthesis of 4,5-Fused cis-and trans-2,3-DihydrofuransThe conformationally fixed vinyloxiranes 7c - f, 8a - f, and 9b - d are transformed thermally into the bicyclic ethers 23 - 25. Starting with the spiro-derivatives c - f, which are monosubstituted at the vinyl group, the ring expansion takes place with high stereospecificity leading to 4,5-fused cis-(c/e) and trans-2,3-dihydrofurans (d/f), respectively. On heating 8b and 9b in the presence of dimethylfumarate besides the isomerisation to 24b/25b two cycloadducts are formed in each case to which the structures of 29/31 and 30/32 have been assigned. Oxapentadienyl dipoles (3) are proposed as intermediates in which the rotation of C/O-bonds is energetically more favorable than rotation of C/C-bonds. The activation parameters for the transformation 8b → 24b are determined and discussed together with the reported data of some analogous ring expansion reactions.
    Notes: Die konformativ fixierten Vinyloxirane 7c - f, 8a - f und 9b - d wandeln sich thermisch mit Ausbeuten zwischen 50 und 80% in die bicyclischen Ether 23 - 25 um. Ausgehend von den an der Vinylgruppe monosubstituierten Spiro-Derivaten c - f erfolgt die Ringerweiterungsreaktion mit hoher Stereospezifität zu 4,5-anellierten cis- (c/e) bzw. trans-2,3-Dihydrofuranen (d/f). Beim Erhitzen von 8b und 9b in Gegenwart von Fumarsäuredimethylester entstehen neben den Isomeren 24b bzw. 25b jeweils zwei Cycloaddukte im Verhältnis 10: 1, denen die Strukturen 29/31 und 30/32 zugeordnet werden. Als Zwischenstufen werden Oxapentadienyl-Dipole (3) angenommen, in welchen die Rotation um C/O-Bindungen energetisch günstiger ist als die um C/C-Bindungen. Die Aktivierungsparameter der Umwandlung 8b → 24b werden bestimmt und im Zusammenhang mit denen einiger analoger Ringerweiterungen diskutiert.
    Additional Material: 12 Tab.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 941-954 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Statistical Syntheses of RotaxanesThe acetalisation of the 28-membered cyclic diols 11a, b with the long-chain dibromo ketone 12 gives acetals 13a, b. These compounds react with triphenylmethyllithium to give 17a, b and 18a, b from which the rotaxanes 20a, b are obtained in 0.066 or 0.18 and 0.12% yield, respectively, after hydrolysis of the acetal bonds. The reacetalisation of rotaxane 20b affords, by an intraannular reaction, the prerotaxane 18b in pure form.
    Notes: Die Acetalisierung der 28-gliedrigen cyclischen Diole 11a, b mit dem langkettigen Dibromketon 12 ergibt die Acetale 13a, b. Nach Umsetzung mit Triphenylmethyllithium zu 17a, b und 18a, b werden nach Hydrolyse der Acetalbindungen die Rotaxane 20a, b in Ausbeuten von 0.066 und 0.18 bzw. 0.12% als farblose Öle isoliert. Durch Reacetalisierung von 20b wird in einer intraannularen Reaktion das Prärotaxan 18b in reiner Form erhalten.
    Additional Material: 1 Ill.
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