Zobrazeno 1 - 10
of 27
pro vyhledávání: '"R. G. Bistline"'
Publikováno v:
Organic Syntheses
α-Sulfopalmitic acid reactant: Palmitic acid (200 g., 0.78 mole) reactant: sulfur trioxide, 53 ml. (100 g., 1.25 moles) product: α-Sulfolauric acid product: α-Sulfomyristic acid product: α-Sulfopalmitic acid product: α-Sulfostearic acid product:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8414839c14571c84d85e528b8ec7dd6f
https://doi.org/10.1002/0471264180.os036.30
https://doi.org/10.1002/0471264180.os036.30
Publikováno v:
Journal of the American Oil Chemists' Society. 57:98-103
A series of fatty acid amides anilides was prepared and a number of compounds in the series were found to be highly active against gram positive bacteria but ineffective against gram negative organisms. The N,N-dimethyl- and N,N-diethylamides of C12-
Publikováno v:
Journal of the American Oil Chemists Society. 39:55-58
A series of sodium alkyl α-sulfopelargonates prepared from sodium α-sulfopelargonic acid and alcohols of from 2 to 12 carbon atoms were examined for surface active properties. Esters with the hydrophilic portion in the middle of the molecule, as in
Publikováno v:
Journal of the American Oil Chemists Society. 37:679-682
Direct sulfonation of higher fatty acids with sulfur trioxide or chlorosulfonic acid, without use of solvent, is possible, but the product must then be isolated as the sodium salt. Use of a chlorinated solvent permits isolation of the α-sulfo acid.
Publikováno v:
Journal of the American Oil Chemists Society. 39:128-131
A series of esters of the general formula RCH(SO3Na)-CO2R′ of 14–19 carbon atoms prepared by the α-sulfonation of propionic, butyric, pelargonic, lauric, myristic, palmitie, and stearic acids and esterification with normal primary alcohols were
Publikováno v:
Journal of the American Oil Chemists' Society. 40:538-541
Even chain sodium alkanesulfonates from the Strecker reaction, odd chain sodium alkanesulfonates from the alkaline decarboxylation of α-sulfo acids, and sodium 1-hydroxy-2-alkanesulfonates from the reduction of esters of α-sulfo acids were compared
Publikováno v:
Journal of the American Oil Chemists' Society. 34:100-103
Publikováno v:
Journal of the American Oil Chemists' Society. 44:99-102
Saturated (I, ROSO3Na) and unsaturated (II, R’OSO3Na) tallow alcohol sulfates, the disodium salt ofa-sulfonated saturated tallow fatty acids (III, RCH(SO3Na)CO2Na), the sodium salt of the methyl ester ofa-sulfonated saturated tallow fatty acids (IV
Publikováno v:
Journal of the American Oil Chemists' Society. 42:1078-1081
Lithium, ammonium, sodium, potassium, magnesium, and calcium salts of methyl, ethyl, propyl, isopropyl, butyl, isobutyl and secondary butyl esters ofa-sulfopalmitic anda-sulfostearic acids were prepared for a study of structureproperty relations. The
Autor:
C. C. Litchfield, Henry Rakoff, Renȳ Maire, R. T. Holman, M. R. Subbaram, C. G. Youngs, M. J. McCarthy, A. Kuksis, J. R. Trowbridge, A. B. Herrick, R. A. Bauman, B. M. Craig, M. K. Bhatty, N. Sen, H. Schlenk, J. L. Gellerman, E. A. Emken, R. O. Butterfield, M. L. Blank, Margaret Farquhar, Raymond Reiser, F. E. Luddy, R. A. Barford, S. F. Herb, R. W. Riemenschneider, J. J. Peifer, R. Muesing, F. Janssen, J. A. Schmit, Dmytro Buchnea, E. J. Dufek, W. J. DeJarlais, R. O. Feuge, Zigrida Zarins, H. W. Kircher, A. E. Johnston, C. A. Glass, I. R. Schmolka, M. Cenker, M. Kokorudz, H. K. Mangold, C. R. Houle, R. G. Bistline, A. J. Stirton, E. D. Berglund, S. B. Crecelius, Irving Cohen, Peter Economou, W. G. Spangler, Henry Watanabe, W. L. Groves, D. A. Netzel, C. W. Stanley, D. W. Rathburn, R. A. Reck, N. M. Molnar, S. Baron, E. C. Horning, W. L. Holmes, J. G. Hamilton, J. E. Muldrey, Grace A. Goldsmith, G. P. Shulman, W. E. Link, H. Y. Lew, C. T. Desmond, W. T. Borden, L. Gildenberg, D. P. Lundgren, H. J. Keily, E. A. Knaggs, L. Varenyi, J. A. Yeager, E. Fischer, J. K. Weil, J. Morrisroe, R. W. Atwood, R. E. Temple, D. C. Malins, J. C. Wekell, R. A. Morrissette, Helen Ven Horst, W. K. Rohwedder, E. Selke, C. R. Scholfield, A. P. Tulloch, H. H. O. Schmid, W. O. Lundberg, J. A. Harris, F. C. Magne, E. L. Skau, J. E. Mehrens, C. F. Smullin, A. D. Cooper, N. Tuna, M. Heimberg, N. B. Fizette, H. Klausner, M. Horning, S. E. Mayer, P. A. T. Swoboda, C. H. Lea, J. R. Chipault, G. R. Mizuno, R. H. Anderson, T. E. Huntley, Helen A. Moser, C. D. Evans, W. F. Kwolek, F. D. Hill, E. G. Hammond, W. D. Pohle, R. L. Gregory, B. Van Giessen, T. J. Weiss, J. R. Taylor, J. J. Ahern, J. H. Rolker, A. E. Rheineck, Sol Shulman, B. G. Brand, H. O. Schoen, L. E. Gast, J. C. Cowan, S. C. S. Peng, D. L. Wood, L. L. Hopper, F. G. Dollear, D. D. Zimmerman, D. G. Therriault, J. F. Taylor, U. Westphal, J. D. Mullen, D. E. Smith, G. R. Riser, F. W. Bloom, L. P. Witnauer, R. R. Mod, E. W. Bell, J. P. Friedrich, G. Maerker, E. T. Haeberer, W. C. Ault, H. E. Kenney, Daria Komanowsky, A. N. Wrigley, Abner Eisner, Theodore Perlstein, R. E. Beal, P. Fitton, E. H. Pryde, B. J. Mayland, R. L. Harvin, C. R. Trimarke, E. N. Frankel, V. L. Davison, E. Emken, A. F. Mabrouk, H. Lavery, H. B. Oakley, N. V. Lovegren, B. Bradshaw, W. E. Scott, C. F. Krewson, J. Oswald, L. S. Crauer, H. Pennington, Fairie Lyn Carter, V. L. Frampton, J. E. McGhee, L. D. Kirk, G. C. Mustakas, E. L. Griffin, L. E. Allen, O. B. Smith, R. K. Downey, L. T. Black, K. A. Jurbergs, D. J. Dowling, Walter Szutowicz, Mary E. McKillican, J. M. Bell, J. J. Rahm, Hans Kaunitz, Ruth Ellen Johnson, Merle Blank, O. S. Privett, V. Mahadevan, E. Cubero, D. Sand, G. L. Feldman
Publikováno v:
Journal of the American Oil Chemists' Society. 40:9-45