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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 89 (1977), S. 670-671 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 90 (1978), S. 566-567 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 4-Alkyl(Aryl)-λ5-phosphorins; 1,4-Dihydrophosphorin/λ5-Phosphorin4 RearrangementThe 1-R'-4-R-4-methoxy-1,4-dihydrophosphorins11-17, the 1H- and 13C-NMR spectra and stereochemistry of which are discussed, are formed by reaction of (1 Z, 4Z)-1,5-dilithio-3-R-3-methoxy-1,4-pentadienes9 with R'PCl2 [R' = aryl, alkyl, N(C2H5)2, OC4H9, SC6H5] at - 78°C. Addition of catalytic amounts of acid causes rearrangement of the 1,4-dihydrophosphorins and yields the 1-R'-1-methoxy-4-R-λ5-phosphorins23 - 29 which represent the most simple derivatives of this class of compounds. - The mechanism of this 1,4-dihydrophosphorin/λ5-phosphorin rearrangement has been studied; according to that a direct H+-catalyzed 1,4-migration of the methoxy group is assumed concerning the trans-isomers, while the 1-R'-phosphorinium cations are intermediates in the case of the cis-isomers. - Acid-catalyzed hydrolysis of the λ5-phosphorins yields the 1-R'-4-R-1,2-dihydrophosphorin oxides35. The 1,1-dimethoxy-4-R-λ5-phosphorins28 have been prepared by direct oxidative alkoxylation of the λ3-phosphorins with Hg(OAc)2/methanol.
    Notes: Durch Umsetzung der (1 Z,4Z)-1,5-Dilithio-3-R-3-methoxy-1,4-pentadiene9 mit R'PCl2 [R' = Aryl, Alkyl, N(C2H5)2, OC4H9, SC6H5] bei - 78°C werden die 1-R'-4-R-4-methoxy-1,4-dihydrophosphorine11 - 17 erhalten, deren 1H- und 13C-NMR-Spektren und cis/trans-Stereochemie diskutiert werden. - Die 1,4-Dihydrophosphorine lagern sich bei der Einwirkung von katalytischen Mengen Säure in die entsprechenden 1-R'-1-methoxy-4-R-λ5-phosphorine23-29 als bisher einfachste Vertreter dieser Verbindungsklasse um. Ihre 1H-NMR-, 13C-NMR-, UV-, IR- und Massenspektren werden diskutiert. - Der Mechanismus dieser 1,4-Dihydrophosphorin/λ5-Phosphorin-Umlagerung wird untersucht; danach muβ angenommen werden, daβ sich die trans-Isomeren in einer direkten H + -katalysierten 1,4-Verschiebung der Methoxygruppe umlagern, während bei den cis-Isomeren die 1-R'-phosphoriniumkationen Zwischenstufe sind. - Bei der säure-katalysierten Hydrolyse der λ5-Phosphorine entstehen die 1-R'-4-R-1,2-dihydrophosphorinoxide35. Die 1,1-Dimethoxy-4-R-λ5-phosphorine28 lassen sich direkt durch oxidative Alkoxylierung der λ3-Phosphorine mit Hg(OAc)2/Methanol darstellen.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 4-Alkyl(Aryl)-λ3-phosphorins from Butoxy-4-alkyl(aryl)-4-methoxy-1,4-dihydrophosphorinsThe (1 Z,4Z)-1,5-dilithio-3-R-3-methoxy-1,4-pentadienes9 have been obtained by cleavage of 1,1-dibutyl-4-R-4-methoxy-1,4-dihydrostannis1 with butyllithium. Reaction of9 with butoxydichlorophosphorane at -78°C gives the cis/trans-isomeric 1-butoxy-4-R-4-methoxy-1,4-dihydrophosphorins17. Their reduction with LiAlH4 leads to the monosubstituted 4-R-λ3-phosphorins3 [R = CH3, C2H5, C(CH3)3, cyclo-C6H11, C6H5] in good yields. - The 1H-NMR spectra of the λ3-phosphorins are analyzed and computer-simulated, the 13C-NMR, UV, and mass spectra are discussed in detail.
    Notes: Die aus 1,1-Dibutyl-4-R-4-methoxy-1,4-dihydrostanninen1 durch Spaltung mit BuLi erhältlichen (1 Z,4Z)-1,5-Dilithio-3-R-3-methoxy-1,4-pentadiene9 reagieren mit Butoxydichlorphosphan bei -78°C zu den cis/trans-isomeren 1-Butoxy-4-R-4-methoxy-1,4-dihydrophosphorinen17. Durch deren Reduktion mit LiAlH4 werden in guten Ausbeuten die monosubstituierten 4-R-λ3-phosphorine3 [R = CH3, C2H5, C(CH3)3, cyclo-C6H11, C6H5] erhalten. - Die 1H-NMR-Spektren der λ3-Phosphorine werden analysiert und simuliert, die 13C-NMR-, UV- und Massenspektren werden ausführlich diskutiert.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1985 (1985), S. 1093-1094 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Note on the Synthesis of 3-[Alkyl(Aryl)thio]isoindolinones from Methyl 2-FormylbenzoateIn a one-pot procedure the isoindolinone derivatives 6 have been obtained from methyl 2-formylbenzoate, primary amines, and thiols via the intermediate imines 1.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1980 (1980), S. 2095-2125 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 4-Alkyl-, 4-Aryl-Δ3-arsenines and 4-Alkyl-, 4-Aryl-2-benzyl-Δ3-arsenines by 4-Methoxy-1,4-dihydroarsenine-Arsenine RearrangementThe (1 Z, 4 Z)-1,5-dilithio-(3R)-3-methoxy-1,4-pentadienes (R = alkyl, aryl) react with tert-butyl-(dichloro)arsine to give the E/Z-isomeric 1-tert-butyl-(4R)-4-methoxy-1,4-dihydroarsenines, which undergo H+-catalyzed aromatization to the 4R-arsenines. The 1H-NMR-, 13C-NMR- and mass spectra of the 1,4-dihydroarsenines and arsenines are discussed. The 1-(diethylamino)-(4R)-4-methoxy-1,4-dihydroarsenines are transformed by reaction with hydrochloric acid  -  depending on the nature of R  -  into the 1-chloro-(4R)-4-methoxy-1,4-dihydroarsenines [R = C(CH3)3] or 2-chloro-(4R)-arsenines (R = C6H5). 1-Benzyl-(4R)-4-methoxy-1,4-dihydroarsenine undergoes 1,4-dihydroarsenine-arsenine rearrangement to 2-benzyl-(4R)-arsenine [R = (CH3)3C] on reaction with BF3-etherate.
    Notes: (1 Z,4 Z)-1,5-Dilithio-(3 R)-3-methoxy-1,4-pentadiene (R = Alkyl, Aryl) reagieren mit tert-Butyl-(dichlor)arsin zu den E/Z-isomeren 1-tert-Butyl-(4R)-4-methoxy-1,4-dihydroarseninen, die unter H+-Katalyse zu den 4 R-Arseninen aromatisieren. Die 1H-NMR-, 13C-NMR- und Massen-Spektren der 1,4-Dihydroarsenine und Arsenine werden diskutiert. Die 1-(Diethylamino)-(4 R)-4-methoxy-1,4-dihydroarsenine gehen in Abhängigkeit von R bei der Umsetzung mit Salzsäure in 1-Chlor-(4R)-4-methoxy-1,4-dihydroarsenine [R = C(CH3)3] oder 2-Chlor-(4R)-arsenine (R = C6H5) über. 1-Benzyl-(4R)-4-methoxy-1,4-dihydroarsenin unterliegt bei der Umsetzung mit BF3-Etherat der 1,4-Dihydroarsenin-Arsenin-Umlagerung zu 2-Benzyl-(4R)-arsenin [R = (CH3)3C].
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of 2-Aryl-(4-R)-arsenines by Cyclohexadienol → Arsabenzene RearrangementKOH/[18]crown-6 phase-transfer catalyzed addition of arylarsines (phenylarsine, p-tolylarsine) to the (3-R)-3-methoxy-1,4-pentadiynes 13 yields the cis/trans isomeric 1-aryl-1,4-dihydro-(4-R)-4-methoxyarsenines, the 1H-NMR- and 13C-NMR spectra of which are discussed. - The addition of BF3-etherate or p-toluenesulfonic acid to the 1,4-dihydroarsenines 14, 15 causes rearrangement under 1,2-aryl migration to the 2-aryl-(4-R)-arsenines 22, 24. This rearrangement represents the first element-organic analogue of the cyclohexadienol → benzene rearrangement. The 1H-NMR, 13C-NMR, UV, and mass spectra of the synthesized arsenines 22, 24 are discussed.
    Notes: Durch KOH/[18]Krone-6 phasentransfer-katalysierte Addition von Arylarsanen (Phenylarsan, p-Tolylarsan) an (3-R)-3-Methoxy-1,4-pentadiine 13 werden cis/trans-isomere 1-Aryl-1,4-dihydro-(4-R)-4-methoxyarsenine 14 und 15 erhalten, deren 1H-NMR- und 13C-NMR-Spektren diskutiert werden. - Die 1,4-Dihydroarsenine 14 und 15 lagern sich bei Umsetzung mit BF3-Etherat oder p-Toluolsulfonsäure unter 1,2-Arylverschiebung in die 2-Aryl-(4-R)-arsenine 22 bzw. 24 um. Diese Umlagerung stellt das erste elementorganische Analogon zur Cyclohexadienol → Benzol-Umlagerung dar. Die 1H-NMR-, 13C-NMR-, UV- und Massenspektren der dargestellten Arsenine 22 und 24 werden diskutiert.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 16 (1977), S. 637-639 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 17 (1978), S. 528-530 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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