Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1964, 29, 1466-1475
https://doi.org/10.1135/cccc19641466

Identifizierung der Glycidyläther Bis-phenyl- und Bis-α-naphthylurethane der α-Alkyl(aryl)äther des Glycerins

V. Ulbrich, J. Makeš and M. Jureček

Crossref Cited-by Linking

  • Garcia-Cano Jorge, Gomis Vicente, Font Alicia, Calemma Vincenzo, Gambarotta Enrico Francesco: Vapor-liquid equilibrium of 3-ethoxy-1,2-propanediol + water/ethanol/diethyl ether/glycerol/1,2-propanediol at different pressures. Fluid Phase Equilibria 2020, 512, 112519. <https://doi.org/10.1016/j.fluid.2020.112519>
  • Fekete Szabolcs, Veuthey Jean-Luc, Beck Alain, Guillarme Davy: Hydrophobic interaction chromatography for the characterization of monoclonal antibodies and related products. Journal of Pharmaceutical and Biomedical Analysis 2016, 130, 3. <https://doi.org/10.1016/j.jpba.2016.04.004>
  • Reddy M. Anjun, Reddy L. Rajender, Bhanumathi N., Rao K. Rama: A NOVEL AND EFFICIENT BIOMIMETIC HYDROLYSIS OF OXIRANES TO 1,2-DIOLS CATALYSED BY β-CYCLODEXTRIN IN WATER UNDER NEUTRAL CONDITIONS. Organic Preparations and Procedures International 2002, 34, 537. <https://doi.org/10.1080/00304940209355776>
  • Azari Fereshteh, Nemat-Gorgani Mohsen: Reversible denaturation of carbonic anhydrase provides a method for its adsorptive immobilization. Biotechnol. Bioeng. 1999, 62, 193. <https://doi.org/10.1002/(SICI)1097-0290(19990120)62:2<193::AID-BIT9>3.0.CO;2-H>
  • Taguchi Hiroyasu, Armarego Wilfred L. F.: Glyceryl-ether monooxygenase [EC 1.14.16.5]. A microsomal enzyme of ether lipid metabolism. Med. Res. Rev. 1998, 18, 43. <https://doi.org/10.1002/(SICI)1098-1128(199801)18:1<43::AID-MED3>3.0.CO;2-S>
  • Kim Jong Seung, Bartsch Richard A.: Synthesis of new proton‐ionizable dibenzocrown ethers. Journal of Heterocyclic Chem 1998, 35, 285. <https://doi.org/10.1002/jhet.5570350204>
  • Yuan Hu Geng, Hua Ye Hua, Koiš Pavol, Prónayová Nad'a, Quing Liu, Perjéssy Alexander: CORRELATION ANALYSIS OF IR AND NMR SPECTRAL CHARACTERISTICS OF GLYCIDYL ETHERS. Heterocyclic Communications 1998, 4. <https://doi.org/10.1515/HC.1998.4.1.39>
  • Noe Christian R., Knollmüller Max, Miculka Christian, Dungler Karin, Wagner Ernst, Ettmayer Peter: Chirale Lactole, XI. Eine Methode zur Bestimmung der Absolutkonfiguration chiraler Alkanole. Chem. Ber. 1994, 127, 887. <https://doi.org/10.1002/cber.19941270516>
  • Condon Brian D.: Glycerylbisether sulfates. I: Improved synthesis. J Americ Oil Chem Soc 1994, 71, 739. <https://doi.org/10.1007/BF02541431>
  • Pesliakas Henrikas, Žutautas Vilius, Baškevičiūt≐ Birut≐: Immobilized metal-ion affinity partitioning of NAD+-dependent dehydrogenases in poly(ethylene glycol)-dextran two-phase systems. Journal of Chromatography A 1994, 678, 25. <https://doi.org/10.1016/0021-9673(94)87070-5>
  • KOSAR-HASHEMI Behjat, ARMAREGO Wilfred L. F.: A Convenient Spectrophotometric Method for Measuring the Kinetic Parameters of Glyceryl-Ether Monooxygenase (EC 1.14.16.5). Biological Chemistry Hoppe-Seyler 1993, 374, 9. <https://doi.org/10.1515/bchm3.1993.374.1-6.9>
  • Podzimek Š., Eichler J., Tkaczyk M.: Liquid chromatographic analysis of cationic polymerized phenyl glycidyl ether. Journal of Chromatography A 1991, 547, 195. <https://doi.org/10.1016/S0021-9673(01)88643-X>
  • Ganong Barry R.: Bimodal lipid substrate dependence of phosphatidylinositol kinase. Biochemistry 1990, 29, 6904. <https://doi.org/10.1021/bi00481a021>
  • Voelkel Adam, Szymanowski Jan, Beger Jörg, Ebert Kerstin: Polarity of 1,3-bis[ω-butoxyoligo(oxyethylene)]propan-2-ols as measured by reversed-phase gas chromatography. Journal of Chromatography A 1987, 398, 31. <https://doi.org/10.1016/S0021-9673(01)96493-3>
  • Lee Cherl-Ho, Kim Sung-Koo: Effects of protein hydrophobicity on the surfactant properties of food proteins. Food Hydrocolloids 1987, 1, 283. <https://doi.org/10.1016/S0268-005X(87)80016-4>
  • Matsumoto Ushiho, Shibusawa Yöichi: Surface affinity chromatographic separation of blood cells. Journal of Chromatography A 1986, 356, 27. <https://doi.org/10.1016/S0021-9673(00)91464-X>
  • Brandts P.M., Middelkoop C.M., Gelsema W.J., De Ligny C.L.: Hydrophobic interaction chromatography of simple compounds on alkyl-agaroses with different alkyl chain lengths and chain densities. Journal of Chromatography A 1986, 356, 247. <https://doi.org/10.1016/S0021-9673(00)91486-9>
  • Brandts P.M., Gelsema W.J., De Ligny C.L.: Influence of additives to the eluent on hydrophobic interaction chromatography of simple compounds. Journal of Chromatography A 1986, 354, 19. <https://doi.org/10.1016/S0021-9673(01)87007-2>
  • Hjertén Stellan, Yao Kunquan, Liu Zhao-Qian, Yang Duan, Wu Bo-Liang: Simple method to prepare non-charged, amphiphilic agarose derivatives, for instance for hydrophobic interaction chromatography. Journal of Chromatography A 1986, 354, 203. <https://doi.org/10.1016/S0021-9673(01)87022-9>
  • Nemat‐Gorgani Mohsen, Karimian Khashayar: Interaction of proteins with Triton X‐100‐substituted sepharose 4B. Biotech & Bioengineering 1984, 26, 565. <https://doi.org/10.1002/bit.260260602>
  • Ling T.G.I., Mattiasson B.: Poly(ethylene glycol)- and poly(vinyl alcohol)-substituted carbohydrate gels for “mild” hydrophobic chromatography. Journal of Chromatography A 1983, 254, 83. <https://doi.org/10.1016/S0021-9673(01)88321-7>
  • TAKABAYASHI Kenji, IMADA Teruaki, SAITO Yuji, INADA Yuji: Coupling between fatty acid binding and sulfhydryl oxidation in bovine serum albumin. European Journal of Biochemistry 1983, 136, 291. <https://doi.org/10.1111/j.1432-1033.1983.tb07740.x>
  • NEMAT‐GORGANI Mohsen, KARIMIAN Khashayar: Non‐ionic Adsorptive Immobilization of Proteins to Palmityl‐Substituted Sepharose 4B. European Journal of Biochemistry 1982, 123, 601. <https://doi.org/10.1111/j.1432-1033.1982.tb06575.x>
  • Bostwick J. Robert, Eichberg Joseph: Detergent solubilization and hydrophobic chromatography of rat brain phosphatidylinositol kinase. Neurochem Res 1981, 6, 1053. <https://doi.org/10.1007/BF00964412>
  • Halperin G., Breitenbach M., Tauber-Finkelstein M., Shaltiel S.: Hydrophobic chromatography on homologous series of alkylagaroses. Journal of Chromatography A 1981, 215, 211. <https://doi.org/10.1016/S0021-9673(00)81400-4>
  • Genieser Hans-Gottfried, Gabel Detlef, Jastorff Bernd: Quantitative ether cleavage of ligands in hydrophobic agaroses —precise determination of the degree of substitution. Journal of Chromatography A 1981, 215, 235. <https://doi.org/10.1016/S0021-9673(00)81402-8>
  • Donescu D.: Kinetics of the Polymerization of Ethyl Glycidil Ether and Allyl Glycidil Ether with BF3OEt2. Journal of Macromolecular Science: Part A - Chemistry 1981, 15, 1545. <https://doi.org/10.1080/00222338108056801>
  • Stockton Jane M., Turner Anthony J.: Characterization of Adenylate Cyclase Purified from Rat Brain by Hydrophobic Chromatography. Journal of Neurochemistry 1981, 36, 1722. <https://doi.org/10.1111/j.1471-4159.1981.tb00424.x>
  • HELBIG N. B., HO L., CHRISTY G. E., NAKAI S.: DEBITTERING OF SKIM MILK HYDROLYSATES BY ADSORPTION FOR INTO INTO ACIDIC BEVERAGES. Journal of Food Science 1980, 45, 331. <https://doi.org/10.1111/j.1365-2621.1980.tb02608.x>
  • Dantschev Damjan, Georgiev Atanas, Tschalina Elena, Dobreva‐Usunova Dobrinka, Staneva Duschka: Etherderivate des 3‐Amino‐1,2‐propandiols, 2. Mitt. Synthese und Pharmakologische Untersuchung von N‐substituierten Derivaten des 1‐Cycloalkyloxy‐3‐amino‐2‐propanols. Archiv der Pharmazie 1979, 312, 857. <https://doi.org/10.1002/ardp.19793121012>
  • Georgiev Athanas, Tschalina Elena, Petkov Wesselin, Manolov Petar: Synthese und pharmakologische Untersuchung von Etherderivaten des 3‐Amino‐1,2‐propandiols, 1. Mitt. Archiv der Pharmazie 1979, 312, 881. <https://doi.org/10.1002/ardp.19793121102>
  • Keshavarz Elaheh, Nakai Shuryo: The relationship between hydrophobicity and interfacial tension of proteins. Biochimica et Biophysica Acta (BBA) - Protein Structure 1979, 576, 269. <https://doi.org/10.1016/0005-2795(79)90402-1>
  • Montanari Fernando, Tundo Pietro: Hydroxymethyl 18-crown-6 and hydroxymethyl [2.2.2]cryptand: versatile derivatives for binding the two polyethers to lipophilic chains and to polymer matrices. Tetrahedron Letters 1979, 20, 5055. <https://doi.org/10.1016/S0040-4039(01)86788-5>
  • Lok C.M.: Versatile methods for the synthesis of mixed-acid 1,2-diacylglycerols. Chemistry and Physics of Lipids 1978, 22, 323. <https://doi.org/10.1016/0009-3084(78)90020-8>
  • Allenmark Stig, Servenius Bo: Characterization of bacterial l-(-)-tyrosine decarboxylase by isoelectric focusing and gel chromatography. Journal of Chromatography A 1978, 153, 239. <https://doi.org/10.1016/S0021-9673(00)89878-7>
  • Kißing W., Reiner R. H.: Chromatographic investigation into the interaction between proteins and polymer matrices I. Agarose gels with substituents of different length and hydrophobicity. Chromatographia 1977, 10, 129. <https://doi.org/10.1007/BF02297864>
  • Homcy C.J., Wrenn S.M., Haber E.: Demonstration of the hydrophilic character of adenylate cyclase following hydrophobic resolution on immobilized alkyl residues. Critical role of alkyl chain length. Journal of Biological Chemistry 1977, 252, 8957. <https://doi.org/10.1016/S0021-9258(17)38332-1>
  • P»hlman Sven, Rosengren Jan, Hjertén Stellan: Hydrophobic interaction chromatography on uncharged sepharose® derivatives. Journal of Chromatography A 1977, 131, 99. <https://doi.org/10.1016/S0021-9673(00)80924-3>
  • Hammar Lena, Påhlman Sven, Hjertén Stellan: Chromatographic purification of a mammalian histidine decarboxylase on charged and non-charged alkyl derivatives of agarose. Biochimica et Biophysica Acta (BBA) - Enzymology 1975, 403, 554. <https://doi.org/10.1016/0005-2744(75)90084-4>
  • Rosengren Jan, Påhlman Sven, Glad Magnus, Hjertén Stellan: Hydrophobic interaction chromatography on noncharged sepharose® derivatives. Biochimica et Biophysica Acta (BBA) - Protein Structure 1975, 412, 51. <https://doi.org/10.1016/0005-2795(75)90338-4>
  • Hjertén Stellan, Rosengren Jan, P»hlman Sven: Hydrophobic interaction chromatography. Journal of Chromatography A 1974, 101, 281. <https://doi.org/10.1016/S0021-9673(00)82845-9>
  • Asinger F., Fell B., Pfeifer J., Saus A.: Zur Relativen Reaktivität der Epoxid‐ und Halogengruppe in Epihalogenhydrinen bei der basenkatalysierten Reaktion mit Hydroxyverbindungen. J. Prakt. Chem. 1972, 314, 71. <https://doi.org/10.1002/prac.19723140110>
  • Morton M., Kammereck R. F., Fetters L. J.: Polymerisation and block copolymerisation of cyclic sulphides. Brit. Poly. J. 1971, 3, 120. <https://doi.org/10.1002/pi.4980030303>
  • Koinuma Hideomi, Inoue Shohei, Tsuruta Teiji: Polymerization of epoxyorganosilanes. III. Copolymerization with glycidyl ether. Makromol. Chem. 1970, 136, 65. <https://doi.org/10.1002/macp.1970.021360105>
  • Ponomarenko V.A., Khomutov A.M., Il'Chenko S.I., Gorshkova G.N., Bogdanov V.S.: Characteristics of cationic tetrahydrofuran copolymerization with glycidyl ethers. Polymer Science U.S.S.R. 1969, 11, 206. <https://doi.org/10.1016/0032-3950(69)90026-4>
  • Ulbrich Vladimír, Makeš Jaroslav: Identifizierung von glycidyläthern. Journal of Chromatography A 1964, 15, 371. <https://doi.org/10.1016/S0021-9673(01)82794-1>