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  • 1
    Electronic Resource
    Electronic Resource
    Reaktionen von Aroyl(Hetaroyl)iminodithiokohlesäureestern mit Carbanionen CH-acider Verbindungen (1983)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 325 (1983), S. 675-679 
    Details
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of Dimethyl N-Aroyl(Hetaroyl)carbimidodithioates with Carbanions CH-acidic CompoundsReactions of dimethyl N-aroyl(hetaroyl)carbimidodithioates 1 with carbanions 2 present new possibilities to synthesize 3-acyl-amino-3-methylthio-2-subst.-acrylnitriles 3 by monosubstitution of methylthiogroup.The reaction of 1 with 2-alkyl-benzothiazolium salts 4 yield deeply coloured N-acyl-(2,3-dihydrobenzothiazole-2-yliden) thioacetimido acid-methylates 5 of the 2-subst.-benzothiazoliumperchlorates 6. The structures of the final products are determined by i.r.-, 1H.-n.m.r.- and u.v.-spectra.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/prac.19833250417
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  • 2
    Electronic Resource
    Electronic Resource
    Synthese und Reaktionsverhalten von N-(3-Chlorbenzo[b]-thiophen-2-carbonyl)imino-Dithiokohlensäure-Derivaten (1984)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 633-637 
    Details
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis and Reaction Behaviour of N-(3-Chlorobenzo[b]thiophene-2-carbonyl)-imino-dithiocarbonic Derivatives3-Chlorobenzo[b]thiophene-2-carbonyl-chloride 1 was treated with potassium rhodanide to afford the appropriate acyl isothiocyanate 3, which adds nucleophilic agents as amines and thioles in good yields.Addition of methanethiole and subsequent alkylation of the dithiocarbamate 7 gives S, S-dimethylimino-dithiocarbonate 8. 3-Chlorobenzo[b]thiophene-2-carboxamide 2 reacts with carbon disulphide and phenyl isothiocyanate by chlorine substitution and cyclisation to benzo[b]thieno[2, 3-e]thiazines 9, 10 or 11. The structure of the final products were determined by analytical and spectroscopical dates.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/prac.19843260416
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  • 3
    Electronic Resource
    Electronic Resource
    Reaktionen mit N-Acylimino-dithiokohlensäurediestern (1980)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 322 (1980), S. 55-68 
    Details
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions with N-Acylimino-dithiocarbonic-acid-diesters.Reactions of N-acylimino-dithiocarbonic-acid-S,S-diesters 1 with nucleophilic com-pounds present new possibilities to synthesize heterocycles. With amines 1a reacts by mono- and disubstitution, respectively, of methylthio-groups to isothioureas 2 and guanidines 3, with 1,2-bi-nucleophilic arenes to benzoheterocycles 4, with aliphatic diamines to imidazolidines 5, pyrimidines 6, diazepines 7 and the hexamethylene-diamine-derivatives 8. 1a reacts also with hydrazines to 1,2,4-triazoles 9 and with hydrazides to the thiosemicarbazones 10 or 1,3,4-oxadiazoles 11. Heterocyclisations of 1 with guanidines, thiourea, salts of thiourea and amidines give the 1,3,5-triazines 12, 14, 15 and 16. N-benzoyl-dithiocarbonic-acid-methylester -amid reacts with CH-acidic compounds to thiazoles 17. The structures of the final products are determined by i.r.-, 1H-n.m.r.-, u.v.- and mass-spectras.
    Additional Material: 9 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/prac.19803220109
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  • 4
    Electronic Resource
    Electronic Resource
    Eine neue Synthese des Cinnamoyliminodithiokohlensäure-S,S-dimethylesters und Umsetzungen mit Nucleophilen (1980)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 322 (1980), S. 434-444 
    Details
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New Synthesis of Dimethyl-cinnamoylimino-dithiocarboxylate and Reactions with NucleophilesA new general synthesis of dimethyl-cinnamoylimino-dithiocarboxylate 1d is possible by reaction of 4-nitro-cinnamoylamide with carbon disulfide in the presence of sodium hydride and following alkylation. With the unsubstituted dimethyl-cinnamoylimino-dithiocarboxylate 10 is in-vestigated the reaction behavior with nucleophilic compounds. The treatment of 1c with primary amines, respectively, by mono- and disubstitution of the methylthio groups yields isothiourea 2 or guanidines 3. Benzocondensed heterocycles are formed by reaction of 1c with o-bifunctional nucleo-philes.The compounds 5, 6 and 7 have been synthesized from 1c with cysteamine, p-phenylenediamine and ethylenediamine.The oxadiazole 8 and isothiosemicarbazide 9 are obtained by reaction of the dithioester 1c with hydrazides. On the other hand cyclisation to the 1,2,4-triazole 11 over the intermediate 10 and to the 1,3,5-triazine 12 are possible.The reaction of 1c with carbanions in a basic medium affords acrylic derivatives 13.In the same way we isolated by reaction of dithioester 1c with a benzothiazolium salt the dark coloured compound 14. The physical properties of synthesized compounds are discussed by mass-, 1H-n.m.r.-, i.r.- and u.v.-spectra.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/prac.19803220314
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  • 5
    Electronic Resource
    Electronic Resource
    Zum Reaktionsverhalten von Carbonsäureamiden gegenüber Schwefelkohlenstoff und Isothiocyanaten (1982)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 324 (1982), S. 625-630 
    Details
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reaction Behaviour of Amides with Carbondisulphide and IsothiocyanatesReactions of substituted arylamides, hetarylamides and furylacrylicamide 1 with carbon disulphide present a possibility to synthesize imino-dithiocarbonic-S,S′-diester 5. The mechanism of the reaction and the reaction conditions are investigated. Quantum chemical investigations by simple HMO-method in connection with the experimental results describe the reaction in dependence upon the influence of substituent in 2- and 4-position to the phenylring. Further more is described the reaction of amide with isothiocyanates to thiourea 6 and isothiourea 7.The structures of the final products are determined by analytical dates.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/prac.19823240418
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  • 6
    Electronic Resource
    Electronic Resource
    1H- und 13C-NMR-Untersuchungen an N-Acyl-imino-dithio-kohlensäure-S,S-dimethylestern (1983)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 325 (1983), S. 1011-1015 
    Details
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H- and 13C-N.M.R. Investigations of N-Acyl-imino-dithiocarbonic-S,S-dimethylester
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/prac.19833250618
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  • 7
    Electronic Resource
    Electronic Resource
    Über aromatische Derivate der Orthoschwefligsäure (1918)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 416 (1918), S. 291-304 
    Details
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jlac.19184160213
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