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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 9 (1960), S. 1649-1654 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary 1. The action of diethyl ethylphosphonite on chloroacetone results in the formation of ethyl isopropenyl ethylphosphonate. In the case of bromoacetone, as well as ethyl isopropenyl ethylphosphonate, ethyl acetonylethylphosphinate is formed. 2. The reaction of chloroacetone with sodium ethyl ethylphosphonite gives ethyl (1,2-epoxy-1-methylethyl)ethylphosphinate. 3. A study was made of the Raman spectra and ultraviolet absorption spectra of previously undescribed compounds.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The action of diethyl ethylphosphonite onα-chlorocyclohexanone gives cyclohexen-1-yl-1 -ethyl ethylphosphonate, Cyclohenen-1-yl-1-ethyl ethylphosphonate is also obtained by the action of sodium monoethyl ethylphosphonite on a-chlorocyclohexanone.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 9 (1960), S. 780-787 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary 1. On the basis of chemical and spectrographic data it was shown that the product of the action of sodium diethyl phosphite on 2-chlorocyclopentanone is diethyl 1,2-epoxycyclopentylphosphonate. The product of the action of sodium diethyl phosphite on 2 -bromocyelohexanone is a mixture of 1-cyclohexen-1-yl diethyl phosphate and diethyl 1,2-epoxycyclohexylphosphonate. 2. The products of the action of sodium diethyl phosphite and of triethyl phosphite on 2-chloro-2-methyl-cyclohexanone consist of diethyl 2-methyl-1-cyclohexen-1-yl phosphate; the product of the action of triethyl phosphite on 3-bromo-3-methyl-2-butanone is diethyl isopropenyl phosphate. 3. The product of the action of sodium diethyl phosphite on 3-bromocamphor is the corresponding mixed phosphoric ester.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 9 (1960), S. 1129-1133 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The addition of diphenyl phosphite to p-benzoquinone and to 1,4-naphthoquinone in presence of sodium alkoxide led to the formation of diethyl p-hydroxyphenyl phosphate and diethyl 4-hydroxy-1-naphthyl phosphate, respectively.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 1 (1952), S. 773-780 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary 1. The specific viscosities have been determined of dilute solutions in benzene and in carbon tetrachloride of phosphorous and boric esters having long hydrocarbon radicals (from octyl to decyl. Comparison of the values found for ηsp (1.4%) and Zη with those calculated indicates that the molecules of these esters are in the extended form in dilute solution, which is in agreement with parachor data. 2. The specific viscosities have been determined of dilute solutions in benzene and in carbon tetrachloride ] of phosphoric and phosphorotionic esters having hexyl and octyl radicals. Comparison of the values found for ηsp (1.4%) and Zη with those calculated indicates that the molecules of phosphoric and phosphorothionic esters are in the extended form in dilute solution which is not in agreement with conclusions based on a study of the parachors of these esters. 3. When a comparison is made of the found and calculated values of ηsp (1.4%) and Zη for macrocyclic compounds having rings of 15–34 members for which viscosity, data are available in the literature, it is found that the viscosity values found are closer to those calculated for the total number of members in the ring than to those calculated, following Staudinger's views, for a half of that number. 4. Cyclic esters of triethylene glycol with succinic, adipic, and sebacic acids have been synthesized, and viscosity measurements have been made on their dilute solutions. The values found for ηsp (1,4%) and Zη are greater than those calculated for the total number of members in the ring, 5. Our results show that further investigation is required into the question of what measurements of viscosity tell us concerning molecules of branched structure and molecules having branched rings, and they show that further investigation. is required also into the nature of Gibling's corrections for parallelism in the determination of molecular structure by the parachor method.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 10 (1961), S. 1884-1890 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary 1. The reaction of trans-2,6-dibromocyclohexanone with one and two molecules of triethyl phosphite follows a complex course. The reaction with one molecule of triethyl phosphite stops at the stage of formation of the diethyl bromo-6-cyclohexen-1-yl ester of phosphoric acid, which is further converted to diethyl cyclohexadien-1,3-yl-2 phosphate and diethyl phenyl phosphate. The diethyl phosphoric ester of the enol form of the ester of cyclohexanone-2-phosphonic-1 acid is not produced in this process. 2. The cis- and trans-isomers of 2,6-dichlorocyclohexanone reacr with two molecules of triethyl phosphite with the formation of diethyl chloro-6-cyclohexen-1-yl ester of phosphoric acid. 3. The bromination of the diethyl cyclohexenyl ester of phosphoric acid with bromosuccinimide with subsequent treatment with triethyl phosphite does not lead to the diethylphosphoric ester of the enol form of cyclohexan-one-2-phosphonic-1 acid. A mixture of products is formed similar to the mixture obtained when triethyl phosphite acts on cis-2,6-dibromocyclohexanone.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 1 (1952), S. 787-795 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary 1. The following alkylphosphonic esters have been synthesized: dibutyl, dihexyl, dioctyl, and didecyl methylphosphonates; dihexyl hexylphosphonate, dioctyl octylphosphonate, dinonyl nonygphosphonate, and didecyl decylphosphonate. 2. Mixed esters of alkylphosphonic acids, have been obtained for the first time by a transesterification reaction: ethyl hexyl, ethyl octyl, and ethyl decyl methylphosphonates; ethyl hexyl hexylphosphonate, and ethyl octyl octylphosphonate. 3. The parachors of the alkylphosphonic esters have been determined, and conclusions have been reached concerning the corrections for chain interaction.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 10 (1961), S. 1877-1883 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary 1. The reaction of triethyl phosphite with 2,6-dibromocyclohexanone follows a complex course. In addition to the expected diethylphosphoric ester of the enol form of the ester of cyclohexanone-2-phosphonic-1 acid, by-products are formed which are produced by conversions of the latter compound (diethyl ester of cyclohexanone-2-phosphonic-1 acid and tetraethyl ester of hypophosphoric acid), and also an intermediate product, diethyl bromo-6-cyclohexen-1-yl phosphoric ester [diethylcyclohexadien-1,5-yl phosphate, diethyl phenyl phosphate]. 2. The cis- and trans-isomers of 2,6-dibromocyclohexanone react differently with triethyl phosphite. The trans-isomer gives the diethylphosphoric ester of the enol form of the ester of cyclohexanone-2-phosphonic-1 acid as the main reaction product. With the cis-form the diethyl ester of cyclohexanone-2-phosphonic-1 acid is formed. In both cases, the products enumerated in paragraph 1 also are obtained.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 6 (1957), S. 57-66 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary 1. The results reported point to an analogy between β-keto and β-alkoxycarbonyl derivatives of phosphonic and carboxylic esters. 2. Phosphonoacetic and 2-phosphonopropionic triesters do not contain appreciable amounts of the enol forms. 3. Titration with bromine indicates that acetonylphosphonic and 1-methylacetonylphosphonic esters contain small amounts of the enol forms. Considerable enolization occurs in an alkaline medium. 4. β-keto phosphonic esters prepared by the A. E. Arbuzov rearrangement differ in their properties from sodium diethyl phosphite.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary 1. Reaction of triethyl phosphite with chloro- and bromo-acetones* and 1-bromo-2-butanone gives the corresponding β-keto phosphonic esters. 2. The products obtained by methylating the potassium derivatives of diethyl acetonylphosphonate and of diethyl 1-methylacetonylphosphonate with methyl iodide are sB-keto phosphonic esters. 3. Reaction of sodium diethyl phosphite with chloro- and bromo-acetones and 3~bromo-2-butanone gives epoxy phosphonic esters. The structures of these were proved by confirmatory synthesis and by analysis of their Raman spectra. 4. In spite of Kreutzkamp and Kayser's results, reaction of sodium diethyl phosphite with chloro- or bromoacetone does not give an unsaturated ester (diethyl isopropenyl phosphate); the products are diethyl epoxy-1-methylethylphosphonate and diethyl acetonylphosphonate. 5. The product of the reaction of 5-chloro-2-pentanone with sodium diethyl phosphite is diethyl tetrahydro2-methyl-2-furylphosphonate.
    Type of Medium: Electronic Resource
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