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  • 1970-1974  (12)
  • Chemistry  (12)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 315 (1973), S. 965-969 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Bromaddukte 2 von 4-Aryl-trithionen mit H in 5-Stellung reagieren mit aromatischen Aminen zu Isothiazolinthionen-(5) 5, aus denen mit GRIGNARD-Verbindungen 1-Arylamino-3-(methylmercapto oder phenylmercapto)-3-thioxo-2-aryl-propene-(1) 7 erhalten werden.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 742 (1970), S. 103-106 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On 1,2-Dithiacyclopentenes, XIX1). 5-Amino-3-imino-1,2-dithia-4-cyclopentenesThe 5-amino-1,2-dithia-4-cyclopentene-3-imines 5 have been prepared from the dithiolium compounds 4 and aromatic amines.
    Notes: Die Dithiolium-Verbindungen 4 reagieren mit aromatischen Aminen zu den 5-Amino-1.2-dithia-cyclopenten-(4)-iminen-(3) 5.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1973 (1973), S. 241-246 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On 1,2-Dithiacyclopentenes, XXI1). - N-(3H-1,2-Dithiol-3-ylidene)benzamides from 3-Chloro-1,2-dithiolium ChloridesWith the N, N-dichloronitrobenzamides 2a and 2b the 3-chloro-1,2-dithiolium chlorides 1a and 1b react to N-(3H-1,2-dithiol-3-ylidene)benzamides 3. With nucleophilic compounds N-(5-chloro-3H-1,2-dithiol-3-ylidene)benzamides yield the substitution products 5 and 6.
    Notes: 3-Chlor-1,2-dithiolium-chloride 1a und 1b reagieren mit N,N-Dichlor-nitrobenzamiden 2a und 2b zu N-(3H-1,2-Dithiol-3-yliden)benzamiden 3. N-(5-Chlor-3H-1,2-dithiol-3-yliden)-benzamide liefern mit nucleophilen Verbindungen die Substitutionsprodukte 5 und 6.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 734 (1970), S. 173-179 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 1.2-Dithia-cyclopentenes, XVIII1). 3-Amino-4-aryl-5-pyrazolinones from 5-Amino-4-aryl-1.2-dithia-3-cyclopentenones3-Amino-4-aryl-5-pyrazolinones 5-7 are prepared from 5-amino-4-aryl-1.2-dithia-3-cyclopentenones 1; thiomalonic acid derivatives 2 or 3 are intermediates. 4 is formed from 3 and phenylhydrazine; its ring closure proves structure 5.
    Notes: 3-Amino-4-aryl-pyrazolinone-(5)5-7 sind aus 5-Amino-4-aryl-1.2-dithia-cyclopentenonen-(3) 1 über Thiomalonsäure-Derivate 2 bzw. 3 zugänglich. Aus 3 und Phenylhydrazin entsteht 4, dessen Ringschluß Struktur 5 beweist.
    Additional Material: 6 Tab.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1974 (1974), S. 1261-1268 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On 1,2-Dithiacyclopentenes, XXVI1). - Ring Cleavage of 5-Chloro-3H-1,2-dithiol-3-ones by Grignard Compounds5-Chloro-4-phenyl-3H-1,2-dithiol-3-one (1) and 4,5-dichloro-3H-1,2-dithiol-3-one (2) are cleaved by Grignard compounds at the S-S-bond with formation of intermediates which subsequently react to give sulfur heterocycles: Stereoisomeric 1,3-dithietanediylidene bis-(phenylthioacetic acid S-esters) 6 are obtained from 1, and 2-chloro-2-(dithiolidene)thioacetic acid S-esters 12 from 2. Reactions of 6 and 12 with nucleophilic compounds have been studied. The 1,3-dithietanes 6 are cleaved by amines with formation of monothiomalondiamides.
    Notes: 5-Chlor-4-phenyl-3H-1,2-dithiol-3-on (1) und 4,5-Dichlor-3H-1,2-dithiol-3-on (2) werden durch Grignard-Verbindungen an der S-S-Bindung zu Primärprodukten gespalten, die zu Schwefelheterocyclen weiterreagieren: Aus 1 werden stereoisomere 1,3-Dithietandiylidenbis-(phenylthioessigsäure-S-ester) 6, aus 2 2-Chlor-2-(dithioliden)thioessigsäure-S-ester 12 erhalten. - Umsetzungen von 6 und 12 mit nucleophilen Partnern wurden untersucht. Amine spalten die 1,3-Dithietane 6 zu Monothiomalondiamiden 10.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1973 (1973), S. 247-255 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On 1,2-Dithiacyclopentenes, XXII1). - Ring Cleavage of N-(5-Aryl-3H-1,2-dithiol-3-yliden)-arylamines by Grignard CompoundsN-(5-Aryl-3H-1,2-dithiol-3-yliden)arylamines 2 are cleaved by Grignard compounds at the sulfur-sulfur bond to 3-alkylthio(or phenylthio)-1-aryl-3-arylamino-2-propene-1-thiones 3, which are studied.
    Notes: Grignard-Verbindungen spalten N-(5-Aryl-3H-1,2-dithiol-3-yliden)arylamine 2 an der Schwefel-Schwefel-Bindung zu 3-Alkylthio(oder Phenylthio)-1-aryl-3-arylamino-2-propen-1-thionen 3, die untersucht werden.
    Additional Material: 7 Tab.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 734 (1970), S. 164-172 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 1.2-Dithia-cyclopentenes, XVII1) Substitution on the 1.2-Dithia-cyclopenteneimine System5-Chloro- and 5-tosyl-1.2-dithia-cyclopenteneimines (1-5, 12, 14, 19, 20) react with nucleophilic compounds in 5-position. 4 and thiourea yield the 1.2-dithiol-3-thione 24, which is alkylated at the thione group. Alkaline cleavage of 10r yields the thiophenes 37, 38, or 39.
    Notes: 5-Chlor- und 5-Tosyl-1,2-dithia-cyclopentenimine (1-5, 12, 14, 19, 20) reagieren mit nucleophilen Partnern in 5-Stellung zu den Substitutionsprodukten. 4 liefert mit Thioharnstoff das Trithion 24, das am Thion-Schwefel alkyliert wird. Alkalische Spaltung von 10r führt zum Thiophen-System (37-39).
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 741 (1970), S. 153-156 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Perchloro-1,2-dimethylenecyclobutane from HexachloropropenePerchloro-1,2-dimethylenecyclobutane (3) is formed from hexachloropropene (4) and the sodium salt of trichloroacetic acid (5). The presence of perchloroallene (2) as intermediate is proved by studies with labelled compounds.
    Notes: Hexachlorpropen (4) und das Na-salz der Trichloressigsäure (5) reagieren zum Perchlor-1.2-dimethylen-cyclobutan (3). Die Perchlorallen-Zwischenstufe (2) wird mit markierten Verbindungen nachgewiesen.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 766 (1973), S. 1-5 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 1,2-Dithiacyclopentenes, XX1). 3-Chloro-1,2-dithiolium Chlorides from TrithionesThe trithiones 1 react with trichloromethyl isocyanide dichloride (3) or thiophosgene (4) to give the 3-chloro-1,2-dithiolium chlorides 6, which are hydrolyzed to the 1,2-dithiacyclopentenones 2.
    Notes: Die Trithione 1 reagieren mit Trichlormethyl-isocyaniddichlorid (3) oder Thiophosgen (4) zu den 3-Chlor-1.2-dithioliumchloriden 6, welche zu den 1.2-Dithia-cyclopentenonen 2 hydrolysiert werden.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1973 (1973), S. 256-262 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On 1,2-Dithiacyclopentenes, XXIII1). - Heterocycles from 3-Alkylthio-(or Phenylthio)-1-aryl-3-arylamino-2-propene-1-thiones3-Alkylthio(or phenylthio)-1-aryl-3-arylamino-2-propene-1-thiones 1, which are obtained from N-(5-aryl-3H-1,2-dithiol-3-yliden)arylamines and Grignard compounds, are starting materials for isoxazoles, pyrazoles, isothiazolium iodides, metal chelates and quinolines.
    Notes: Aus N-(5-Aryl-3H-1,2-dithiol-3-yliden)arylaminen mit Grignard-Verbindungen zugängliche 3-Alkylthio(oder Phenylthio)-1-aryl-3-arylamino-2-propen-1-thione 1 sind Ausgangsmaterialien für Isoxazole, Pyrazole, Isothiazolium-jodide, Metallchelate und Chinoline.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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