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  • 2000-2004
  • 1995-1999  (1)
  • 1980-1984  (7)
  • 1975-1979  (8)
  • Chemistry  (16)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 320 (1978), S. 313-323 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis of Nitro- and Amino-Substituted Thiobenzamides by Thiolation Reactions with Elemental Sulfur at Mild ConditionsThe Synthesis of thiobenzamides 2-7 by basecatalyzed thiolation of nitro-benzyl-halides (type 1), especially at low temperatures, and the selective synthesis of p- and m-nitro-thio-benzamides (2, 3) or p-and m-amino-thiobenzamides (5, 6), respectively, are described. o-Nitro-benzylhalides (→ 4, 7) are less reactive than p- and m-nitro-benzylhalides.The reaction of nitrobenzylhalides (type 1) with elemental sulfur and amines occuring at low temperatures to give 2-4 leads via structures of the type 11, 15 and 16.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 324 (1982), S. 227-236 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Derivatives of Imidazolidines from Oxalic AmidinesTetraarylsubstituted oxalic amidines 1 react with acyl chlorides, phosgene, thiophosgene, chlorocarbonylsulfenylchloride, isocyaniddichlorides, and N-aroyl-1-chlorothio-formimidoylchlorides 7 to give the corresponding 5-membered heterocycles 3, 4, 5 and 8.Isocyanates 9 and isothiocyanates 10 react with oxalic amidines to yield imidazolidines 11, 12 and ureas 13, 14.Hydrolysis of 3-5, 8, 11, 12 leads to the corresponding oxo compounds 15, 16.
    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 322 (1980), S. 273-280 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Reaction of N-Sulfinylamines with Isocyanides and Synthesis of 2,5-Diaryl-3,4-diarylimino-1,2,5-thiadiazolidin-S-oxidesN-Sulfinylamines 1 react with isocyanides 2 to give isocyanates 3, isothiocyanates 6, and especially 2,5-diaryl-3,4-diarylimino-1,2,5-thiadiazolidin-S-oxides 7.This new heterocyclic ring system 7 can also be synthesized in high yields by a cyclization reaction of tetraarylated oxalic amidines 9 with thionyl chloride.The acid catalyzed hydrolysis of the heterocyclic compounds 7 leads to oxalic anilides 8, the hydrolysis with alkali forms amidines 9. The amidine 9a reacts with N-sulfinyl-p-toluenesulfonamide 11 to give an open chained adduct 12.
    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 325 (1983), S. 174-174 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    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 325 (1983), S. 525-525 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 42 (1996), S. 1789-1792 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 5 Ill.
    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 318 (1976), S. 161-167 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Reactions of 2,1-Benzisothiazolin-3-onesDependent on the substituent group at the nitrogen the sodium salts of thioanthranilic acids 3, availabel from isatoic anhydrides 1 and sodium hydrogen sulphide, yield on oxidation 2,1-benzisothiazolin-3-ones 4 or bis-anthranoyl disulphides 5. The latter are cyclized under special conditions to yield 4. From 4 and oxalyl chloride, 3-chloro-2,1-benzisothiazolium chlorides 7 are available which give with hydrogen sulphide the thiones 6 and with dimethyl aniline the polymethines 9. The dyestuffs 9 can also be prepared from the 3-methylthio-2,1-benzisothiazolium salts 8, obtainable by alkylation of compounds 6.
    Notes: Die aus Isatosäureanhydriden 1 und Natriumhydrogensulfid erhältlichen Natriumsalze der Thioanthranilsäure 3 liefern bei der Oxydation in Abhängigkeit vom Substituenten am Stickstoff 2.1-Benzisothiazisothiazolinone-(3) 4 oder Dianthranoyl-disulfide 5. Die 5 können unter speziellen Bedingungen zu 4 cyclisiert werden. Aus 4 sind mit Oxalychlorid 3-Chlor-2.1-benzisothiazoliumchloride 7 zugänglich, die mit Schwefelwasserstoff zu den Thionen 6 und mit Dimethyl-anilin zu den Polymethinen 9 reagieren. Die Farbstoffe 9 können auch aus den durch Alkylierung der 6 zugänglichen 3-Methylmercapto-2.1-benzisothiazoliumsalzen 8 dargestellt werden.
    Additional Material: 2 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 318 (1976), S. 221-228 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of 3-Amino-1,2-dithiolium Salts and their Conversion to 2-Nitro-3-aminothiophenes3-Amino-1.2-dithiolium salts 2a-1 are easily available from 3-chloro-1,2-dithiolium salts 1 and secondary amines.A new procedure to prepare 2-nitro-3-aminothiophenes 3 starting from N,N-substituted 3-amino-5-phenyl-1,2-dithiolium salts 2 is described which consists in a nucleophilic exchange of a sulfur atom for the carbon atom of nitromethane.The structure of 3 has been confirmed by reductive cyclization and by spectroscopic methods.
    Notes: 3-Amino-1.2-dithioliumsalze 2a-1 sind in einfacher Weise aus 3-Chlor-1.2-dithioliumsalzen 1 und sekundären Aminen zugänglich.Es wird ein neues Verfahren zur Herstellung von 2-Nitro-3-amino-thiophenen 3 aus N,N-disubstituierten 3-Amino-5-phenyl-1.2-dithioliumsalzen 2 durch nucleophilen Austausch eines Schwefelatoms gegen das C-Atom des Nitromethans beschrieben. Die Struktur der Thiophene 3 wird durch reduktive Cyclisierung und spektroskopische Methoden gesichert.
    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 318 (1976), S. 359-368 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of 4-Arylazo-isoxazolium Salts4-Arylazo-isoxazolium salts (3, 4), a new class of cationic dyes, are now available by alkylating the isoxazoles 5 and by reacting 1,3-dicarbonyl compounds of the type 1 with N-alkyl-hydroxylamines, respectively.In contrast to the isothiazole system the alkylation of isoxazoles 5 at the ring nitrogen atom does not cause a significant bathochromic shift.4-Arylazo-5-methoxy-isoxazolium salts (8) can be prepared by alkylating 4-arylazo-isoxazolin-5-ones (6 or 11) with dimethyl sulfate.The analogous reaction with 4-arylazo-5-alkylthio-isoxazolines (12, 13) failed, however, the expected 4-arylazo-5-alkylthio-isoxazolium salts (e. g. 14) can be obtained from 12 and trialkyloxonium fluoborate.
    Notes: Es werden Synthesewege für die bisher unbekannten 4-Arylazo-isoxazoliumsalze (z. B. 3, 4, 8, 14), einer neuen Klasse kationischer Farbstoffe, angegeben. 3 bzw. 4 sind durch Alkylierung der Isoxazole 5 bzw. durch Umsetzung von 1,3-Dicarbonylverbindungen des Typs 1 mit N-Alkylhydroxylaminen zugänglich. Im Gegensatz zum Isothiazolsystem kommt es bei den Isoxazolen 5 nach Alkylierung des Ringstickstoffes kaum zu einer Farbvertiefung.4-Arylazo-5-methoxy-isoxazoliumsalze (z. B. 8) sind durch Alkylierung der 4-Arylazo-isoxazolinone-(5) (6 bzw. 11) mit Dimethylsulfat darstellbar. Eine analoge Reaktion mit den 4-Arylazo-5-alkylmercapto-isoxazolen (z. B. 12, 13) gelingt nicht; die erwarteten 4-Arylazo-5-alkylmercapto-isoxazoliumsalze (z. B. 14) sind jedoch aus 12 und Triäthyloxoniumfluoborat synthetisierbar. Für 12, 13 und die 4-Arylazo-isoxazolinthione-(5) (9, 10) werden einfache präparative Vorschriften angegeben.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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