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Barton, George

Enrique Iglesia, David G. Barton, Stuart L. Soled Sabato Miseo Joseph E. Baumgartner William E. Gates, Gustavo A. Fuentes and George D. Meitzner ... [Pg.533]

One of the most prominent papers to come from the Aspinall group, published with George Zweifel in 1957, reported on the selective tosylation of the 2,3-diols of methyl 4,6-O-benzyl idene-a-D-mannopyranoside (with axial and equatorial hydroxyl groups, respectively, at C-2 and C-3), and 1,6-anhydro-/i-D-mannopyranose (with a confor-mationally inverted pyranose chair, and therefore with equatorial and axial hydroxyl groups, respectively, at C-2 and C-3). In each case the equatorial hydroxyl group was esterified preferentially, consistent with the Barton/Cookson generalization,... [Pg.6]

C. R. Johnson, in Comprehensive Organic Chemistry (Eds. Sir Derek Barton and W. D. Ollis), Vol. 3, pp. 241 ff S. Bleisch and R. Mayer, in Methoden der Organischen Chemie (Houben-Weyl), Band Ell (Ed. D. Klamann), Georg Thieme Verlag, Stuttgart, 1985, pp. 1031 ff. [Pg.761]

Barros EJ, Wehtje E, Adlercreutz P (2000) Mass transfer studies on immobUizEd a-chymotrypsin biocatalysts prepared by deposition for use in organic medium. Biotechnol Bioeng 59 364-373 Barton LL, Georg) CE, Lineback DR (1972) Effect of maltose on glucoamylase formation by Aspergillus niger. J Bacteriol lll(3) 771-777... [Pg.40]

In 1898, George Barton patented a new process where molten lead was rapidly stirred and atomised into small droplets, which were then carried away and oxidised by a humidified air stream drawn through die pot. The resulting oxide was passed through a series of cyclone classifiers where the larger particles were separated and returned back to the reaction pot for further processing, while the fine powder was collected in silos (drums or hoppers). [Pg.13]

In 1898, George V. Barton proposed a method that made the production process of lead oxide considerably faster and easier. This method yields partially oxidized lead powder (leady oxide) which ensures high battery performance. [Pg.227]

Balmer, Johann J., 133 Baltimore, David, 133 Bamberger, Eugen, 133 Barbiturate, 201 Bardeen, John, 181 Barger, George, 133 Bartlett, Neil, 133, 215 Bartlett, Paul D., 133 Barton, Sir Derek H.R, 133-134, 154, 236 Bases, 131, 178, 220,237 Battery, 145,193-194, 202, 220 see also Leyden jar Voltaic pile... [Pg.265]

Sodium 0-ethyl xanthate in acetone added with stirring at —35° during 30 min. to phenacetyl chloride in the same solvent, after 1 hr. allowed to warm to room temp. 0-ethyl S-phenacetyl xanthate (Y 97%) in refluxing dioxane irradiated 3 hrs. with a Hg-arc lamp, and the resulting S-benzyl 0-ethyl xanthate refluxed 1 hr. in 1 9 aq. ale. 1 N NaOH a-toluenethiol (Y 96%). The acyl xanthates are smoothly converted into acyl and xanthate radicals. The former are de-carbonylated and recombine with the xanthate radicals. F. e. and limitations s. D. H. R. Barton, M. V. George, and M. Tomoeda, Soc. 1962, 1967. [Pg.412]

Towrie, M., Grills, D.C., Dyer, L., Weinstein, J.A., Matousek, R, Barton, R., Bailey, R.D., Subramaniam, N., Kwok, W.M., Ma, C., Phillips, D., Parker, A.W. and George, M.W. (2003) Development of a broadband picosecond infrared spectrometer and its incorporation into an existing ultrafast time-resolved resonance Raman, UV/visible, and fluorescence spectroscopic apparatus. Appl. Spectrosc., 57, 367-380. [Pg.305]


See other pages where Barton, George is mentioned: [Pg.368]    [Pg.316]    [Pg.504]    [Pg.1569]    [Pg.163]    [Pg.1162]    [Pg.434]    [Pg.84]    [Pg.165]    [Pg.766]    [Pg.113]    [Pg.1708]    [Pg.977]    [Pg.707]    [Pg.316]    [Pg.142]    [Pg.515]    [Pg.907]    [Pg.109]    [Pg.277]    [Pg.290]    [Pg.289]    [Pg.181]   
See also in sourсe #XX -- [ Pg.13 , Pg.227 ]




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