ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • General Chemistry  (73)
  • Organic Chemistry  (59)
  • 550 - Earth sciences  (13)
  • Electronic structure and strongly correlated systems  (11)
Collection
Keywords
  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 2 (1989), S. 585-601 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Triarylaminium salts smoothly catalyze the cyclopropanation of dienes, styrenes and tetrasubstituted alkenes by ethyl diazoacetate. The reactions are regioselective and, in the case of additions to conjugated dienes, cyclopropane-periselective. A cation radical chain mechanism involving carbene transfer from ethyl diazoacetate to a substrate cation radical is proposed.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 645-650 
    ISSN: 1434-1948
    Keywords: Aziridines ; Coordination ; Ring opening ; Metallacycle ; N-Chirality ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photolytically induced CO substitution reactions of CpMn(CO)3 with N-phenylaziridine and of W(CO)6 with 2,2-dimethylaziridine lead to the N-coordinated aziridine complexes Cp(CO)2Mn{N(Ph)CH2CH2} and (CO)5W{N(H)CH2CMe2}. Both are stable with respect to thermal alkene elimination. The thermal reaction of Cp(CO)3MoCl with N-hydroxyethylaziridine leads to the metallaheterocyclic compound Cp(CO)2MoNH(CH2CH2OH)CH2CH2C(O). It might be formed by several reaction steps including a Cl migration with nucleophilic ring opening, a CO insertion reaction forming the β-aminoacyl ligand and finally a hydrolytic process. The X-ray structure analysis of Cp(CO)2Mn{N(Ph)CH2CH2} and (CO)5W{N(H)CH2CMe2} shows three-membered-ring ligands N-bonded to the metal atoms with a trigonal pyramidal configuration at the nitrogen atoms. The X-ray structure analysis of Cp(CO)2MoNH(CH2CH2OH)CH2CH2C(O) reveals a five-membered heterocyclic ring system, including the molybdenum atom, a carbonyl function and an ammonium center.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 327 (1985), S. 383-398 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two-Phase Reaction of 1-Bromooctane with Sodium Acetate and Potassium Acetate Catalyzed by Diquaternary Ammonium SaltsNew unsaturated diquaternary ammonium salts (diquats) were prepared in two ways from ditertiary amines 3 and 1-bromoalkanes or from 1, 4-dibromobut-2t-ene and tertiary monoamines. A comparison of their catalytic ability with that of saturated diquats and with that of corresponding monoquats was made. The reaction of n-C8H17Br with NaOAc or KOAc in the two-phase system liquid-liquid without an additional solvent is catalyzed more effectively by the unsaturated diquats than by the saturated diquats and the monoquats. Most of the used quats catalyze the ester formation from NaOAc more effectively in the system liquid-liquid, however, the ester formation from KOAc more effectively in the system solid-liquid; KOAc is generally superior to NaOAc in both systems. Consequently, in the phase-transfer catalyzed ester formation from alkali acetate and alkyl halides not only the structure of the quat but also the inorganic cation of the acetate have influence on the rate of conversion.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 328 (1986), S. 407-412 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complex Catalysis with Technetium Compounds. Hydroformylation with Technetiumcarbonyl CatalystsThe hydroformylation reaction of cyclohexene (1), propene (2) and 1-octene (3) was studied using Tc2(CO)10 and Tc(CO)10/P(n-C4H9)3, resp., as catalysts in solution. For comparison experiments have also been made with Mn2(CO)10, Mn2(CO)10/P(n-C4H9)3 and Re2(CO)10/P(n-C4H9)3 as catalysts for the hydroformylation of 1.There is always a competition between hydrogenation and hydroformylation.Tc2(CO)10/P(n-C4H9)3 gave the best results in activity and selectivity within the subgroup VII complexes studied, but is a rather poor catalyst compared with the cobalt or rhodium compounds.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 324 (1982), S. 142-144 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On the Synthesis of Dimethallyl- and Allylmethallyloxalate
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 323 (1981), S. 607-615 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On the Pyrolysis of CycloalkenoaromaticsThe products of pyrolysis of tetraline (1), indane (2), 2-methylindane (3), and tetrahydroacenaphthene (4) in mixtures of n-paraffins were analyzed by gas chromatography. Results show that by temperatures between 700° and 800°C and residence times of about 0.2 s more than 80% of the reaction products are aromatics. The main pathway of the decomposition of 1, 2, and 4 is the dehydrogenation in direction to the corresponding complete aromatic systems or indene respectively. In the case of 3 we found less than 10% of 2-methylindene but more than 40% of skeleton isomeres. The formation of skeleton isomeres can be explained by the concept of radical rearrangements.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 340 (1998), S. 733-737 
    ISSN: 0941-1216
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: L-Malic acid (2) reacts with trifluoroacetic anhydride under anhydrous conditions to give (S)-trifluoroacetoxy-succinic acid anhydride (3). The anhydride 3 undergoes regioselective ring opening with an excess of anilines or primary aliphatic amines leading to N-substituted-(S)-3-hydroxy-succinamic acids (4a-g). Structural elucidation of the reaction products 4a-g was based on analytical and spectroscopic data and on an X-ray structure analysis of 4b. Secondary aliphatic amines react with 3 by condensation and subsequent elimination to furnish N,N′-disubstituted fumaric acid amides 5a, b. Some N-substituted-2-hydroxysuccinamic acids (7a,b) were also prepared for spectral comparison with the 3-hydroxy compounds.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 337 (1995), S. 375-378 
    ISSN: 0941-1216
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The palladium-catalyzed reaction of iodobenzene, p-haloiodobenzenes (p-C6H4IX′; X′=F, Cl, Br, I) and p-dibromobenzene with 4-vinylcyclohexene (Heck arylation reaction of olefins) was investigated with Pd(OAc)2/PR3/Et3N (R=phenyl, o-tolyl) as a classical catalyst system and with Pd(OAc)2/KOAc/[BzEt3N]Cl in DMF as a phase-transfer catalyst system, respectively. Iodobenzene reacts with 4-vinylcyclohexene to give (E)-2-(cyclohex-3-enyl) vinylbenzene (1) as main product. p-Haloiodobenzenes react with 4-vinylcyclohexene to give (E)-p-halo-2-(cyclohex-3-enyl) vinylbenzene (3), p-halo-1-(cyclohex-3-enyl) vinylbenzene (4) or (E,E)-p-bis[2-(cyclohex-3-enyl)vinyl]benzene (5) depending on the reaction conditions and the catalyst system used. The phase-transfer catalyst system is less reactive but more selective. A reaction temperature of 80°C is necessary for reaction with p-dibromobenzene. The investigations demonstrate the much higher reactivity of the exocyclic double bond of 4-vincylcyclohexene in comparison with the endocyclic one.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 2 (1944), S. 115-136 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Es wird gezeigt, daß zwischen starken und schwachen Inhibitoren (Reglern) kein grundsätzlicher sondern nur ein gradueller Unterschied besteht. Ihrer Wirkung nach lassen sich die Inhibitoren und damit auch die Regler in folgende 4 Klassen einteilen:I. Abbruchregler, welche eine zusätzliche Abbruchreaktion verursachen und daher die Reaktionsgeschwindigkeit und den Polymerisationsgrad im gleichen Verhältnis herabsetzen.II. Startregler, welche die Startgeschwindigkeit durch Beseitigung eines Teiles des „Primärproduktes“ hemmen.III. Start-Abbruchregler, welche die Wirkung I und II kombinieren.IV. Kompensationsregler, welche auf den Start beschleunigend wirken, zugleich aber den Kettenabbruch noch stärker beschleunigen, so daß im ganzen eine Verlangsamung der Bruttogeschwindigkeit erfolgt.Durch gleichzeitige Messung der Reaktionsgeschwindigkeit und des Polymerisationsgrades kann man für jeden Inhibitor leicht entscheiden, welcher Klasse er angehört, und seine charakteristischen Reaktionskonstanten bestimmen. Eine vorläufige Übersicht über eine Anzahl von Inhibitoren wird gegeben.Der starke Inhibitor Chinon gehört zur Klasse IV, da er nicht nur die Ketten abbricht, sondern auch den Primärakt stak beschleunigt.-Die Länge der Induktionsperiode ist unter Stickstoff der Chinonkonzentration ungefähr proportional. Sauerstoff verlängert die Induktionsperioden derart, daß diese Proportionalität verschwindet. Die Verlängerung beruht wahrscheinlich darauf, daß bei der Inhibierung entstandenes Hydrochinon wieder zum Chinon regeneriert wird. Die Zusammenhänge zwischen Induktionsperiode, reaktionskinetischer Kettenlänge und Polymerisationsgrad werden erörtert.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 13 (1961), S. 272-284 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Es wurden die IR-Spektren des Glykokollbetains (Dimethylaminoessigsäure-methylbetain) und seines Chlorids sowie diejenigen der Salze des Methylesters, Amids und Nitrils aufgenommen und die Absorptionen weitgehend den Schwingungen der Trimethylammoniumeinheit und der anderen funktionellen Gruppen zugeordnet.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...