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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 122 (1989), S. 19-24 
    ISSN: 0009-2940
    Keywords: Bis(diorganoboryl)chalcogenides ; Pyrazaboles ; Pyrazoles ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Neuartige Substituierte B2ElVIN2 HeterocyclenDie Bis(diorganoboryl)chalkogenide (R2B)2O [R = C2H5 (3); R2 = 1,5-C8H14 (1)], (R2B)2S [R2 = 1,5-C8H14 (5)], und (R2B)2Se [R2 = 1,5-C8H14 (7)] reagieren mit Pyrazol (Pz) und dessen Derivaten 3-Methylpyrazol (3-MePz) und Indazol (benzo-Pz) in hohen Ausbeuten (65-92%) zu stabilen 1:1-Additionsverbindungen [z. B. 2 (El = O), 4 (El = O), 6 (El = S), 8 (El = Se)]. 1H-, 13C-, 11B-NMR-Spektren und Röntgenstrukturanalysen (von 2 und 6) zeigen eine Grundstruktur mit einem zentralen B2ElN2-Heterocyclus (El = O, S, Se). Die Reaktion von 2 mit R2BH und die Thermolyse von 4 führen zu den dimeren 1-Pyrazolylboranen 9a bzw. 9b.
    Notes: The bis(diorganoboryl) chalcogenides (R2B)2O [R = C2H5 (3); R2 = 1,5-C8H14 (1)], (R2B)2S [R2 = 1,5-C8H14 (5)], and (R2B)2Se [R2 = 1,5-C8H14 (7)] react with pyrazole (Pz) and its derivatives 3-methylpyrazole (3-MePz) and indazole (benzo-Pz) to form in high yields (65-92%) stable 1:1 adducts [e.g. 2 (El = O), 4 (El = O), 6 (El = S) and 8 (El = Se)]. 1H-, 13C-, 11B-NMR spectra and X-ray analyses (of 2 and 6) show a basic structure with a central B2ElN2 (El = O, S, Se) heterocycle. The reaction of 2 with R2BH and the thermolysis of 4 give the dimeric 1-pyrazolylboranes 9a and 9b, respectively.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 1699-1704 
    ISSN: 0009-2940
    Keywords: Boron-nitrogen heterocycles ; Pyrazoles ; Aminoboranes ; Steric interactions ; Trialkylboranes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Crowded 3,5-disubstituted pyrazoles, e. g. 3,5-di-tert-butyl-,3,5-di-tert-butyl-4-methyl-, or 3,5-di-tert-butyl-4-ethylpyrazole [(tb)2Pz, (tb)2mPz, or (tb)2ePz, respectively], fail to react with activated trialkylboranes (e. g. BEt3* or BPr3*) at 110°C, even after prolonged heating. At 170°C the reaction of (tb)2Pz with activated triethylborane gives the monomeric diethyl(3,5-di-tert-butyl-1-pyrazolyl)borane (3). At 220-230°C the dimeric boracycles (4)2 are mainly formed [X-ray structure of (4a)2]. In contrast, the reactions of these crowded pyrazoles with tetraalkyldiboranes(6) commence just above room temperature. Diethylhydroborane adducts (5) of 3 and dimeric alkyl(3,5-di-tert-butyl-1-pyrazolyl)-boranes (2b)2 and (2c)2 are the main products.
    Additional Material: 1 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 122 (1989), S. 1231-1236 
    ISSN: 0009-2940
    Keywords: Bis(diorganoboryl) chalcogenides ; Pyrazoles ; N-Base-Organoboron adducts ; Molecular rearrangement ; Fluctuation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Strukturelle Voraussetzungen für die Bildung der B2ElVIN2-FünfringeDie Reaktionen der Bis(diorganoboryl)chalkogenide (R2B)2ElVI [R = Et, ElVI = O (9); R2 = 1,5-C8H14 (1, ElVI = O), (2, ElVI = S)] mit 3-Methyl-, 3,5-Dimethyl-, 3-Methyl-5-phenyl-, 3,5-Diphenyl-, und 3,5-Di-tert-butylpyrazole [mPz, m2Pz, mpPz, p2Pz, und (tb)2Pz] werden untersucht. mPz reagiert mit 2 zu m5, das durch sterische Wechselwirkungen der Methyl-Gruppen von mPz mit dem C-Gerüst von 2 destabilisiert ist und sich in Toluol leicht in den neuen Heterocyclus 7 (Röntgenstrukturanalyse) umwandelt. m4 (El = O) (aus mPz und 1) ist demgegenüber bis 100°C stabil. 1 bildet mit m2Pz und mpPz keine Heterocyclen des Typs 4, sondern die 1:1-Additionsverbindungen m2Pz-1 und mpPz-1 mit zwischen den zwei Bor-Atomen von 1 fluktuierenden Pz-Basen. Zwischen 1 und mpPz lassen sich nur schwache, zwischen 1 und p2Pz bzw. (tb)2Pz keine Wechselwirkungen nachweisen. 9 reagiert mit m2Pz, mpPz und p2Pz zu den Heterocyclen des Typs 10. Zwischen (tb)2Pz und 9 werden keine Wechselwirkungen beobachtet (1H-, 11B-, 13C-NMR).
    Notes: The reactions of the bis(diorganoboryl) chalcogenides (R2B)2ElVI [R = Et, ElVI = O (9); R2 = 1,5-C8H14 (1, ElVI = O), (2, ElVI = S)] with 3-methyl-, 3,5-dimethyl-, 3-methyl-5-phenyl-, 3,5-diphenyl-, and 3,5-di-tert-butylpyrazole [mPz, m2Pz, mpPz, p2Pz, and (tb)2Pz, respectively] have been investigated. mPz reacts with 2 to form the heterocycle m5, which due to the interaction of the methyl substituent with the carbon skeleton of 2 is unstable and readily rearranges to the novel heterocycle 7 (X-ray analysis) when dissolved in toluene at room temperature. In contrast the analogues m4 (El = O), formed from mPz and 1, is stable even when heated at 100°C. The reaction of 1 with m2Pz and mpPz does not produce stable heterocycles of the type 4, instead the 1:1 adducts m2Pz-1 and mpPz-1 are formed in which the pyrazole fluctuates between the two boron atoms of 1. The diboryl oxide 1 showed only weak interactions with mpPz and none with p2Pz and (tb)2Pz. With 9 the pyrazoles m2Pz, mpPz, and p2Pz from readily the corresponding heterocycles 10, however no reaction was observed with (tb)2Pz (1H-, 11B-, 13C-NMR).
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