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  • Organic Chemistry  (11)
  • Wiley-Blackwell  (11)
  • Oxford University Press
  • 1985-1989  (2)
  • 1980-1984  (9)
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  • Wiley-Blackwell  (11)
  • Oxford University Press
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 324 (1982), S. 537-544 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: α-Substituted Phosphonates. 39. Methane-diphosphonic Esters by U.V.-Induced Michaelis-Becker-ReactionDibromomethane resp. chlorbromomethane reacts with sodium dialkyl phosphite in heptane-/liq.NH3 or in liq. NH3 by u.v. irradiation at low temperatures to give in good yields methane diphosphonic acid tetraalkylesters 1. In the same manner with sodium diethyl thionophosphite the corresponding methane-bis-thiophosphonic acid tetraethylester 4 is obtained.
    Additional Material: 2 Tab.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 324 (1982), S. 545-549 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: α-Substituted Phosphonates. 40. 1-Trimethylammonium-1-diethylphosphono-1-cyanomethylid, a Stable N-YlidDiethyl-1-dimethylamino-1-cyanomethanephosphonate 4 can be alkylated on nitrogen to the quarternary ammoniumsalts 5, which by C-deprotonation gives the stable N-ylid 8. The N-ylid 8 behaves inert against carbonyl compounds and acylating agents, but can be C-alkylated and  -  involving an ester-dealkylation  -  C-chlorinated.
    Additional Material: 1 Tab.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 327 (1985), S. 904-907 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Structure of “;Trichloro-diphenoxyphosphorane”The structure of ‘Trichloro-diphenoxyphosphorane’ synthesized by well-known and new methods is not a pentacoordinated phosphorus compound, but has the structure of tetraphen-oxyphosphonium hexachlorophosphate 4.
    Additional Material: 1 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 325 (1983), S. 437-445 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: α-Substituted Phosphonates. 43. Synthesis and Reactivity of 1,2,3,4-Tetrahydroisochinolin-1-phosphonatesN-Alkyl- and N-arylsubstituted 1,2,3,4-tetrahydroisochinolin-1-phosphonates 1 have been synthesized from the corresponding 3,4-dihydroisochinoliniumbromides 7 and triethyl-phosphite. The N-unsubstituted 1,2,3,4-tetrahydroisochinolin-1-phosphonate 10 is available starting from the 1,2,3,4-tetrahydroisochinolin-1-phosphonic acid by esterification with triethylformate and splitting off the formyl group of the primarily formed N-formyl derivative 14. - N-Quarternated tetrahydroisochinolines 19 and the 1-phosphorylated derivatives 17, respectively react with triethyl-phosphite in an unexpected way by dealkylation and not by splitting off the isochinolinring. - By Horner-synthesis with 1 the 1-aralkylidene-isochinolines 23 are available in moderate yields.
    Additional Material: 4 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 323 (1981), S. 939-950 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis and Reactions of 2-Aryloxy-s-trithianes2-Aryloxy-s-trithianes 4 had been prepared from 1-tosyl-imino-1-SIV-1,3,5-trithiane and phenolates. - By self-condensation of 4 1,5-bis-(trithianyl)-1,3,5-trithiapentane 5 and triphenyl-orthoformate 7 are formed, accompanied by further products, which had been isolated in pure state and identified unambiguously by H-n.m.r. and mass-spectra. In the presence of acids the 2-aryloxy-s-trithianes 4 react with nucleophilic aromatic compounds such as phenoles, N,N-dimethylaniline, pyrrole, indole, and thiophenes to give the C-trithianylated products. With mercaptanes 2-alkylthio-s-trithianes are formed.
    Additional Material: 1 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 328 (1986), S. 231-236 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: α-Substituted Phosphonates. 47. Splitting of P—C-Bonds from Trisphosphoryl CompoundsHexaethyldimethylaminomethyl-trisphosphonate (2a) reacts with HCl or trimethylsilylbromid/water by splitting off one phosphoryl group, giving dimethylaminomethyl-bisphosphonic acid (7). The result of methylation of 2a depends on the reagent: with methyliodide one phosphoryl group is split off, and the ammonium salt 11a is formed, while with methyl toluene sulfonate or dimethylsulfate the expected quarternary ammonium salts 10b or 10c are formed. One phosphoryl group of 10c is split off under acidic as well as alkalinous conditions: acidic hydrolysis gives the bisphosphonic acid 15, while under alkalinous conditions the known ylid 16 is formed.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 322 (1980), S. 327-328 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Note on the Synthesis of β-Hydroxyethanephosphonic Acid
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 322 (1980), S. 902-908 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aldehydes, tert. Amines or Acetales from Amidacetales and Grignard-CompoundsAmidacetales 1 or -mercaptales 9 respectively react with Grignard-agents dependent on molar ratio by exchange of methoxy- or methylthio group via not isolable O,N- or S,N-acetales to the corresponding aldehydes 4 or the tert. amines 3. Starting from bicyclic amidacetales 6 aldehydes or bis-β-hydroxyethylamines 8 are formed. By quaternisation of the amidacetal-nitrogen followed by reaction with Grignard-agents the corresponding O,O-acetales are formed.
    Additional Material: 4 Tab.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 323 (1981), S. 353-359 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis of β-Nitroalkenyl-benzylphosphorylderivativesStarting from methoxy-chlormethylbenzaldehydes 2 the benzylphosphonates and -phosphinoxides 3 A, B had been synthesized, which could be transformed via the Schiff-bases 4 A, B to phosphorylated nitrostyrenes 5 A, B and nitropropenylbenzenederivatives 6 A, B. The phosphonoacids 3 Ad, 3 Bd and 6 Ba could be prepared from the corresponding esters by direct acidic hydrolysis or by dealkylation with trimethylsilylbromide and hydrolysis of the trimethylsilylesters respectively.
    Additional Material: 2 Tab.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 323 (1981), S. 877-886 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: α-Substituted Phosphonates. 37. Derivatives of α-Pyrrolomethanephosphonic Acid and N-VinylpyrrolesDiethyl α-aminomethanephosphonate 5a and its α-aryl derivatives 5b-d react with 2,5-diethoxytetrahydrofuran 1 to give diethyl α-pyrrolomethanephosphonate 9a and the α-aryl derivatives 9b-d, respectively. The pyrrolo derivatives 9 can be converted into the lithium salts 15 and 16, respectively, which with carbonyl compounds undergo the HORNER reaction yielding E/Z-mixtures of N-vinylpyrroles 18. In certain cases the intermediate of the HORNER reaction, the β-hydroxyphosphonate 17, can be isolated. The pyrrolo-analogue of stilbene, 18a, is formed only as E-isomer. On treating the lithium salts 15 and 16 with 9 or with alkyl halides α-C-alkylated pyrrolo-phosphonates 22 and 23, respectively, are obtained.
    Additional Material: 6 Tab.
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