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
Collection
Publisher
Years
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 3387-3396 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Chemistry of Amino Oximes, X. The Reactions of,synω- Aminopropiophenone Oximes with Phosgene and 1,1′carbonyldimidazole;- primesyn-ω-(Benzylamino)propiophenone oximes react with phosgene to give 3-(benzylamino)propionanilides (3). 1,7-dioxoperhydrodiphyrimido [3,4-b:3′,4′-e][1,4,2,5]dioxadiazines (5), and 7-oxo-4,5,6,7-tetrahydro-1,2,6-oxadiazepines (4) as main products. The reaction with 1,1′-carbonyldiimidazole leads preferably to 5. The Structures were proved by spectroscopic and chemical methods.
    Notes: Aus syn-ω-(Benzylamino)propiophenon-oximen werden mit Phosgen neben 3-(Benzylamino)-propionaniliden (3) und 1,7-Dioxoperhydrodipyimido[3,4-b:3′,4′-e][1,4,2,5]dioxadiazinen (5) als Hauptprodukt 7-Oxo-4,5,6,7-oxadiazepine (4) erhalten. Die Reaktion führt mit 1,1′-Carbonyldimidazol überwiegend zu 5. Die Strukturen wurden auf spektroskopischen und chemischen Wegen bestimmt.
    Additional Material: 3 Tab.
    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 113 (1980), S. 3373-3376 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Chemistry of Amino Oximes, XII. Synthesis and Properties of 4,5,6,7-Tetrahydro-1,2,6-oxadiazepines4,5,6,7-Tetrahydro-1,2,6-oxadiazepines (2a - d) were prepared by the reaction of the syn-(E)-(benzylamino)propiophenone oximes 1a - d with formaldehyde. The ω-aminopropiophenone oximes 1e - g react with acetone or benzaldehyde to give azomethines 6e - g and 7e - g, respectively.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 3380-3386 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Chemistry of Amino Oximes, IX. The Synthesis and the Configuration of ω-Aminopropiophenone OximesThe synthesis of ω-aminopropiophenone oximes (6) by hydrazinolysis of ω-phthalimidopropiophenone oximes (5) is described. Both the ω-amino- and the ω-phthalimidopropiophenone oximes show syn(Z) configuration, proved by Beckmann rearrangement and u. v. spectra. The reaction with phosgene leads to the anilides 8, formed from 6 by Beckmann rearrangement, and the bisamides derived from 6 and 8.
    Notes: Die Synthese von ω-Aminopropiophenon-oximen (6) durch Hydrazinolyse der ω-Phthalimido-propiophenon-oxime (5) wird beschrieben. Sowohl die ω-Amino-als auch die ω-Phthalimidopropio-phenon-oxime haben syn(Z)-Konfiguration, wie die Beckmann-Umlagerung und die UV-Spektren zeigen. Mit Phosgen entstehen aus 6 durch Beckmann-Umlagerung die Anilide 8, sowie die sich aus 6 und 8 ableitenden Bisamide.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1984 (1984), S. 1696-1701 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Chemistry of Amino Oximes, XVIII. - The Cyclocondensation of (E)-β-(Chloroacetylamino)propiophenone Oxime DerivativesThe (E)-β-(chloroacetylamino)propiophenone oximes 2a-c cyclocondense by reaction with alkali to form 3,11-diphenyl-1,9-dioxa-2,6,10-14- tetraazacyclohexadeca-2,10-diene-7,15-diones 3a-c. From (E)-β-[(benzyl)(chloroacetyl)amino]propiophenone oximes 5a-c the 6-benzyl-5,6-dihydro-3-phenyl-4H- 1,2,6-oxadiazocin-7(8H)-one derivates 6a-c are formed.
    Notes: Die (E)-β-(Chloracetylamino)propiophenon-oxime 2a-c werden durch Alkali zu 3,11-Diphenyl-1,9-dioxa-2,6,10,14-tetraazacyclohexadeca-2,10-dien-7,15-dionen 3a-c cyclokondensiert. Aus (E)-β-[(Benzyl)(chloracetyl)amino]propiophenon-oximen 5a-c entstehen dagegen die 6-Benzyl-5,6-dihydro-3-phenyl-4H-1,2,6-oxadiazocin-7(8H)-on-Derivate 6a-c.
    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...