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  • 1975-1979  (4)
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Family process 18 (1979), S. 0 
    ISSN: 1545-5300
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Psychology
    Notes: Remarriage is analyzed from the perspective of family boundaries and roles. The nuclear and remarriage family models are compared, and the process that begins with the formation of the first-marriage nuclear family and ends with the formation of a second-marriage family is conceptualized in terms of changing family boundaries and roles. Discussions with remarriage group members provide concrete illustrations of this process and suggest solutions to some of the problems confronting remarriage family members.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of marital and family therapy 2 (1976), S. 0 
    ISSN: 1752-0606
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Psychology
    Notes: This paper discusses the special attributes of the legally reconstituted families formed when divorced persons who have children from their previous marriages remarry. The remarriage family is identified as a high risk group for which society has not as yet established norms. Interviews with 70 couples suggest that the stress for couples and families involved in divorce and remarriage would be prevented or reduced through remarriage preparation courses.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1979 (1979), S. 443-445 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of 5-Hydroxy-1,7-naphthyridineN-(p-Toluenesulfonyl)glycine ester 1b reacts with 2-(bromomethyl)nicotinic ester 2 to form the nicotinic acid derivative 3b. Cyclization of 3b, by elimination of sulfinic acid, leads to the 1,7-naphthyridine derivative 7, from which the title compound 8 is formed.
    Notes: N-(p-Toluolsulfonyl)glycinester 1b reagiert mit 2-(Brommethyl)nicotinsäureester 2 zum Nicotinsäurederivat 3b. Dieses läßt sich unter Eliminierung von Sulfinsäure zum 1,7-Naphthyridin-derivat 7 cyclisieren, aus dem die im Titel genannte Verbindung 8 erhalten wird.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1977 (1977), S. 1457-1460 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of Sulfinic Acids with Electron-attracting Substituents in the β-PositionSymmetric sulfones 4 activated by electron-attracting substituents in the β-position react with cyanide or thiophenolate to give activated sulfinic 5 and nitriles 6 or thioethers 7, respectively.
    Notes: Symmetrische Sulfone 4, die in β-Stellung durch elektronenziehende Substituenten aktiviert sind, reagieren mit Cyanid oder Thiophenolat zu aktivierten Sulfinsäuren 5 und Nitrilen 6 bzw. Thioethern 7.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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