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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Intensive care medicine 22 (1996), S. 909-915 
    ISSN: 1432-1238
    Keywords: Key words Acute pancreatitis ; Necrotizing pancreatitis ; Octreotide ; Treatment ; Systemic complications ; SIRS ; ARDS ; Circulatory shock
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract   Objective: To determine the efficiency of intravenous infusion of octreotide in the treatment of patients with severe pancreatitis and pulmonary failure. Design: Prospective, case–control study. Setting: Intensive care unit of a university hospital. Patients: Treatment group: 39 patients with necrotizing pancreatitis were selected for the study. In all, pulmonary failure developed under conservative treatment and surgical intervention had been necessary because of local (abscess, necrosis) or systemic (systemic inflammatory response syndrome) complications. The outcome was prospectively followed up until death or discharge from the hospital. Control group: 54 case–control matched patients with acute necrotizing pancreatitis and pulmonary failure, who had not been treated with octreotide. Intervention: Each patient in the treatment group received 100 μg intravenous octreotide three times daily for 10 days, in addition to the standard intensive care therapy. Results: The groups (octreotide group, control group) were highly comparable with regard to age (mean age: 54, 51 years), sex, severity of illness (Acute Physiology and Chronic Health Evaluation II score: 27, 27), etiology of pancreatitis, and pretreatment at the time of admission to the intensive care unit. There was no difference in the development of renal, hepatic, gastrointestinal, hemostatic, neurologic, or local complications. But the frequency of the adult respiratory distress syndrome (18 vs 40%; p〈0.05) and circulatory shock (51 vs 87%; p〈0.05) was significantly lower in the treatment group. Furthermore, mortality was 26% (10 of 39 patients) in the octreotide group and 61% (33 of 54 patients) in the control group (p〈0.01). Conclusion: The results of our case–control study showed a beneficial effect of octreotide in patients with severe necrotizing pancreatitis and pulmonary failure. Based on these data, a prospective, double-blind, placebo-controlled study should be performed to evaluate these results.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Intensive care medicine 22 (1996), S. 909-915 
    ISSN: 1432-1238
    Keywords: Acute pancreatitis ; Necrotizing pancreatitis ; Octreotide ; Treatment ; Systemic complications ; SIRS ; ARDS ; Circulatory shock
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Objective To determine the efficiency of intravenous infusion of octreotide in the treatment of patients with severe pancreatitis and pulmonary failure. Design Prospective, case-control study. Setting Intensive care unit of a university hospital. Patients Treatment group: 39 patients with necrotizing pancreatitis were selected for the study. In all, pulmonary failure developed under conservative treatment and surgical intervention had been necessary because of local (abscess, necrosis) or systemic (systemic inflammatory response syndrome) complications. The outcome was prospectively followed up until death or discharge from the hospital. Control group: 54 case-control matched patients with acute necrotizing pancreatitis and pulmonary failure, who had not been treated with octreotide. Intervention Each patient in the treatment group received 100 μg intravenous octreotide three times daily for 10 days, in addition to the standard intensive care therapy. Results The groups (octreotide group, control group) were highly comparable with regard to age (mean age: 54, 51 years), sex, severity of illness (Acute Physiology and Chronic Health Evaluation II score: 27, 27), etiology of pancreatitis, and pretreatment at the time of admission to the intensive care unit. There was no difference in the development of renal, hepatic, gastrointestinal, hemostatic, neurologic, or local complications. But the frequency of the adult respiratory distress syndrome (18 vs 40%;p〈0.05) and circulatory shock (51 vs 87%;p〈0.05) was significantly lower in the treatment group. Furthermore, mortality was 26% (10 of 39 patients) in the octreotide group and 61% (33 of 54 patients) in the control group (p〈0.01). Conclusion The results of our case-control study showed a beneficial effect of octreotide in patients with severe necrotizing pancreatitis and pulmonary failure. Based on these data, a prospective, double-blind, placebo-controlled study should be performed to evaluate these results.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 324 (1982), S. 669-672 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Arylation of Thiocarbonyl Compounds by Arenediazonium Salts
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 324 (1982), S. 873-881 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis and Oxydation of 1-(1,3-Thiazol-2-yl)-pyrazolidin-3-onesThe 1-(1,3-thiazol-2-yl)-pyrazolid-3-ones 4 are synthesized by reaction of 1-thiocarbamoyl-pyrazolidin-3-one 2 with α-halogenaldehydes and α-halogenketones, respectively. The structure of 4 is proved by their 1H-n.m.r. and mass spectra. Oxydative dimerisation of 4 leads to the bisazomethinimines 10. The compounds 10 represent a new type of azomethinimines with a quinoid structure.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 479-484 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tetrathiafulvalenes. XXI. Syntheses of Tetrathiafulvalenes from 2-Alkylthio-, 2-Arylthio- and 2-Alkylseleno-1,3-dithiolium SaltsIn the reaction of 2-alkylthio-, 2-arylthio- or 2-alkylseleno-1, 3-dithiolium salts with trivalent phosphorus compounds in acetonitril tetrathiafulvalenes 2 are formed. As an intermediate we suppose a phosphorane, which reacts with further 1,3-dithiolium salt to provide the tetrathiafulvalene. By the application of a 2-alkylthio-1,3-dithiolium salt a monomethin dye is formed in a side reaction. When the reaction is carried out in methanol, the phosphorane is trapped by the solvent and a 2H-1,3-dithiolium salt is obtained.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 545-555 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: About Chlorination of N-Aryl-2,4-dimethyl-buta-1,3-dien-1,4-sultamesThe sultames of structure 1 are easily chlorinated by sulfurylchloride, chlorine or tertbutylhypochlorite. The structure of the mono-(2a-c,3a, d), di-(4a-d), tri- (5c, d) and pentachlorosultames (6a, b) is determined by 13C-n.m.r. spectroscopy. Contrary to the bromination the chlorination (by SO2Cl2) starts with the substitution of the sultamring (formation of mono- and di-chlorosultames) followed of the substitution of the (C-4)-CH3- group (formation of trichlorosultames). By 1,4-addition of an other molecule of chlorine to 5 the pentachlorosultames 6a, b are obtained. Already by recrystalisation of 6a, b in an alcohol the chlorine in 4-position is exchanged by the corresponding alkoxy group (CH3O, C2H5O, n-C3H7O) and the compounds 7-9 are formed.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 329 (1987), S. 811-816 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organic Electron Conductors and Precursors. V. Synthesis of Poly (organylthio-acetylenes)Poly(bis-organylthio-acetylenes) 2 and poly(mono-organylthio-acetylenes) 3 have been synthesized by complex catalyzed polymerization of the corresponding acetylenes (4 resp. 5). Yields and properties of the polymers 2, 3 depend on reaction conditions, the catalyst and the nature of the acetylenes. Relations between these influence factors are discussed.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 327 (1985), S. 428-432 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Iodation of N-Aryl-2,4-dimethyl-buta-1,3-dien-1,4-sultamesBy the iodation of N-aryl-2,4-dimethyl-buta-1,3-dien-1,4-sultames 1 with I2/HgO in EtOH/AcOH the 1,2-thiazine ring is substituted. The monosubstitution occurs on the 1-position (1a, d) and the disubstitution on the 1,3-position (3a). By iodine monochloride in CHCl3 the sultames 1a-d were substituted in the (C-2)-CH3 group (4a-d), in contrast also to the results of chlorination and bromination of 1. The structure of the products 2, 3, 4 was proved by 13C-n.m.r. spectroscopic data.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 325 (1983), S. 153-156 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: About the Thiocyanation of Dialkyl Acetylendicarboxylates
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 321 (1979), S. 827-834 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis of 2-Heterocyclidenamino-1, 3-diaza-trimethincyaninesThe synthesis of 2-[3-methyl-benzthiazol-(1, 3)-inylidene-(2)-amino]- and of substituted 2-[1, 3-dithiolyliden-(2)-amino]-1, 3-diaza-trimethincyanines is described. The heterocyclic imines 1 react with phosgene or thiophosgene to the corresponding ureas 2 and thiureas 3, respectively. Alkylation of 3 to the 2-alkylmercapto-1, 3-diaza-trimethincyanines 4 and subsequent condensation with imine 1 yields the dyes 5. The chemical and spectroscopical data of cyanines 5 are described.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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