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3 edition of Preparation of bis[4-(3,4 dimethylene-pyrrolidyl)-phenyl] methane as a high temperature reactive oligomer found in the catalog.

Preparation of bis[4-(3,4 dimethylene-pyrrolidyl)-phenyl] methane as a high temperature reactive oligomer

Raphael M Ottenbrite

Preparation of bis[4-(3,4 dimethylene-pyrrolidyl)-phenyl] methane as a high temperature reactive oligomer

by Raphael M Ottenbrite

  • 170 Want to read
  • 14 Currently reading

Published by Dept. of Chemistry, Virginia Commonwealth University, National Aeronautics and Space Administration, National Technical Information Service, distributor in Richmond, Va, [Washington, DC, Springfield, Va .
Written in English


Edition Notes

StatementRaphael M. Ottenbrite, Joseph G. Smith, and Akira Yoshimatsu
SeriesNASA contractor report -- NASA CR-181348
ContributionsSmith, Joseph G, Yoshimatsu, Akira, United States. National Aeronautics and Space Administration
The Physical Object
FormatMicroform
Pagination1 v
ID Numbers
Open LibraryOL18006594M

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Preparation of bis[4-(3,4 dimethylene-pyrrolidyl)-phenyl] methane as a high temperature reactive oligomer by Raphael M Ottenbrite Download PDF EPUB FB2

Process for the preparation of bis(4-aminopyridinium)alkanes by reacting difunctionalized alkanes with 4-aminopyridines in water or a mixture of water and organic by: 3. Process for the preparation of bis- (4-aminopyridinium) alkanes by reacting difunctionalized alkanes with 4-aminopyridines in water or a mixture of water with an organic : Wolfgang Beilfus, Ralf Gradtke, Michael Streek.

The novel pigment 3,3′-(4,4′-biphenyldiylbisthio)bismethyl-1,4-naphthoquinone comprising two naphthoquinone units was successfully synthesized. This pigment exhibits three conformational polymorphs, all of which have different colors (light red, red, and deep red).

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Acylated C-glycopyranosyl thioformamides of d-gluco, d-galacto, and d-xylo configuration were obtained by treating the corresponding glycosyl cyanides with hydrogen sulfide in the presence of triethylamine.

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5-Hydroxyoxopentenoic acid esters can be efficiently transformed into the stable bis-potassium salts of the corresponding 5-hydroxyoxopentenoic acids, from which the sensitive acids are released in situ, the latter being converted into substituted 4-hydroxy-2H-pyranones, pyrazoles and isoxazoles under mild conditions; the efficiency of this method is demonstrated by the first Cited by:.

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