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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 317 (1975), S. 798-806 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Phosphonsäuremonoalkylester bzw. Phosphonsäuren reagieren mit Epoxiden zu Phosphonsäure-alkyl-β-hydroxyalkyl- 5 bzw. -bis-β-hydroxyalkylestern 9 oder zu höhermolekularen Polyglykolestern. Durch intramolekulare Umesterung entstehen aus 5 bzw. 9 beim Destillieren unter Abspaltung von Alkohol bzw. Glykol cyclische Phosphonsäureester 6 bzw. 11.
    Additional Material: 3 Tab.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 318 (1976), S. 607-612 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Derivatives of o-Phenylene Phosphate. XII. Reaction of Ortho-acid Chlorides with Ethylene OxideOrtho-acid chlorides react with ethylene oxide in dependence of their structure either to ortho-acid β-chloroethylester or by splitting off 1,2-dichloroethane to the corresponding carbonyl- and phosphoryl derivatives, respectively. Using this method i. a. pentacovalent P-derivatives (pentaoxyphosphoranes 14, 16) are available.
    Notes: Orthosäurechloride reagieren mit Äthylenoxid je nach Struktur entweder zu Orthosäure-β-chloräthylester oder unter Abspaltung von 1,2-Dichloräthan zu den entsprechenden Carbonyl-bzw. Phosphorylderivaten. Auf diesem Weg sind unter anderem pentacovalente P-Verbindungen (Pentaoxyphosphorane 14, 16) zugänglich.
    Additional Material: 1 Tab.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 320 (1978), S. 128-132 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: O,O- and S,S-Acetals of FormylphosphoniumsaltsFor the synthesis of O,O- resp. S,S-acetals (4) of formylphosphoniumsalts, which are not known as free formylderivatives, is described a simple method, consisting in reaction of tert. phosphin with orthoester and acetyl-halide. O,O-Diarylacetals of the type 4 can be synthesized from tert. phosphine and diaryloxychlormethane.
    Additional Material: 1 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 318 (1976), S. 116-126 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: α-Substituted Phosphonates. XIX. Derivatives of Aminomethane-bis-phosphonic AcidAminomethane-bis-phosphonic acid tetraethylesters have been prepared by various methods. Chlorination and hydrolysis of these compounds have been studied in detail.
    Notes: Aminomethan-bis-phosphonsäure-tetraäthylester wurden nach verschiedenen Verfahren synthetisiert. Die Chlorierung und die Hydrolyse dieser Verbindungen wurden eingehend untersucht.
    Additional Material: 3 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 319 (1977), S. 8-16 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: α-Substituted Phosphonates. XXII. Synthesis and N.M.R. Spectra of Open-chain and Cyclic Acetals of Formyl-phosphonic Acid Esters and Formyl-diphenylphosphinoxideThe synthesis of characteristical examples of open-chain and cyclic alkyl-resp. arylacetals of formyl-phosphonic acid esters and of formyl-diphenylphosphinoxide by various methods is described. The 1H-, 13C- and 31P-n.m.r.-spectra of this compounds and their dependence on the structure is discussed.
    Notes: Es wird die Synthese einer Reihe charakteristischer Vertreter offenkettiger und cyclischer Alkyl- bzw. Arylacetale von Formyl-phosphonsäureester und Formyl-diphenyl-phosphinoxid nach verschiedenen Methoden beschrieben. Die 1H-, 13C- und 31P-NMR-Spektren dieser Verbindungen und ihre Abhängigkeit von der Struktur wird diskutiert.
    Additional Material: 4 Tab.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 319 (1977), S. 17-22 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: α-Substituted Phosphonates. XXIII. Synthesis of Open-chain and Cyclic S,S-Acetals of Formyl-phosphonic Acid EstersThe synthesis of open-chain and cyclic alkyl- resp. aryl-S,S-acetals of formylphosphonic acid esters by various methods is described. The 1H-, 13C- and 31P-n.m.r. spectra are discussed.
    Notes: Die Synthese von offenkettigen und cyclischen Alkyl- bzw. Aryl-S,S-acetalen von Formylphosphonsäureestern nach verschiedenen Methoden wird beschrieben. Die 1H-, 13C- und 31P-NMR-Spektren dieser Verbindungen werden diskutiert.
    Additional Material: 2 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 319 (1977), S. 343-346 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 320 (1978), S. 140-142 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Derivatives of o-Phenylenphosphates. XVI. o-Phenylendioxyphosphonium-hexahalogenoantimonatesPentacoordinated o-phenylen-orthophosphate-trihalogenides 1 resp. bis-o-phenylenorthophosphate-chloride 3 can be transformed to stable quasiphosphoniumsalts 2 resp. 4 by reaction with SbCl5 or SbBr3/Br2. The structures of 2 and 4 are confirmed by 31P-n.m.r.
    Additional Material: 1 Tab.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 320 (1978), S. 389-394 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: α-Substituted Phosphonates. XXXI. The Reaction of N,N,N′,N′-Tetramethyl Chloroformamidinium Chloride with P(III) CompoundsN,N,N′,N′-Tetramethyl chloroformamidiniumchloride (4) does not react with triethyl phosphite (TEP) or isopropyl diphenylphosphinate to give the expected bisphosphoryl derivatives 7 and 11, respectively, but primarily the monophosphorylated amidinium salts 6 and 10 respectively. The phosphine oxide 10 is stable, while 6 undergoes an elimination of ethyl chloride to the betain 8. Even under more drastic conditions the reaction of 4 or 8 with TEP does not lead to the expected bis(dimethylamino)bisphosphonate 7, but to the monoaminated bisphosphonate 1, involving a reduction step. Similar reduction has been observed under mild conditions in Michaelis-Arbusov reaction of dichloromethylenimonium chloride, yielding the expected trisphosphonate 2 and the bisphosphonate 1 as a by-product.
    Additional Material: 1 Ill.
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  • 10
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: α-Substituted Phosphonates. XXXIV. Esterification and N-Formylation of α-Aminomethane-bisphosphonic Acids with TriethylorthoformateIn contrast to simple mono- and bisphosphonic acids esterification of dialkylaminomethanebisphosphonic acids with orthoformate (OAE) proceeds very slowly. Monoalkyl and monoarylaminomethanebisphosphonic acids, respectively react with OAE in constrast to analogous hydroxy compounds more readily primarily by formylating the N-atom and then esterification to formyl aminomethane bisphosphonictetraesters 10. Acetaminomethanephosphonic acid (12) reacts without N-formylation, while the aminomethanebisphosphonic acid (14) reacted to give a mixture of mono- and bis-formylated products 15 and 16. By acidic hydrolysis of 10 the ester- and formylgroups are splitt off, while the ester group can selectively be removed by reaction with Me3SiBr/H2O. - As shown by 1H-, 13C- and 31P-n.m.r. spectroscopy the phosphorylated formamides 10 exists in two rotameres, the ratio depending on the solvent. The n.m.r. signals could be correlated to E-resp. Z-form undoubtedly by using shift-agents or the benzene-diluting technique. A rotational barrier of 22,8 kcal for 10c could be calculated.
    Additional Material: 4 Tab.
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