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Organic-Inorganic Hybrid Materials for Efficient Enantioseparation Using Cellulose 3,5-Dimethylphenylcarbamate and Tetraethyl Orthosilicate.
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- Chemistry - An Asian Journal, 2008, v. 3, n. 8/9, p. 1494, doi. 10.1002/asia.200800022
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Enantioseparation using urea- and imide-bearing chitosan phenylcarbamate derivatives as chiral stationary phases for high-performance liquid chromatography.
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- Chirality, 2008, v. 20, n. 3/4, p. 288, doi. 10.1002/chir.20430
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Immobilized polysaccharide derivatives: chiral packing materials for efficient HPLC resolution.
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- Chemical Record, 2007, v. 7, n. 2, p. 91, doi. 10.1002/tcr.20107
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Enantioseparations in nonaqueous capillary liquid chromatography and capillary electrochromatography using cellulose tris(3,5-dimethylphenylcarbamate) as chiral stationary phase.
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- Electrophoresis, 2002, v. 23, n. 3, p. 486, doi. 10.1002/1522-2683(200202)23:3<486::AID-ELPS486>3.0.CO;2-L
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Chiral recognition of cellulose tris(5-fluoro-2-methylpheylcarbamate) toward ( R)- and ( S)-1,1′-bi-2-naphthol detected by negative ion fast-atom bombardment mass spectrometry.
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- Rapid Communications in Mass Spectrometry: RCM, 1999, v. 13, n. 20, p. 2011, doi. 10.1002/(SICI)1097-0231(19991030)13:20<2011::AID-RCM747>3.0.CO;2-O
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Syntheses and Properties of Enantiomerically Pure Higher (n ≥ 7) [n−2]Triangulanedimethanols and σ-[n]HelicenesPreliminary communication: A. de Meijere, A. F. Khlebnikov, S. I. Kozhushkov, K. Miyazawa, D. Frank, P. R. Schreiner, C. Rinderspacher, D. S. Yufit, J. A. K. Howard, Angew. Chem.2004, 116, 6715–6719; Angew. Chem. Int. Ed.2004, 43, 6553–6557.
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- Chemistry - A European Journal, 2006, v. 12, n. 22, p. 5697, doi. 10.1002/chem.200600111
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Cover Picture: Synthesis and Properties of the First Möbius Annulenes (Chem. Eur. J. 21/2006).
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- Chemistry - A European Journal, 2006, v. 12, n. 21, p. 5407, doi. 10.1002/chem.200690064
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Synthesis and Properties of the First Möbius Annulenes.
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- Chemistry - A European Journal, 2006, v. 12, n. 21, p. 5434, doi. 10.1002/chem.200600215
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Bullvalene Trisepoxide and Its Stereospecific Rearrangement to 2,8,12-Trioxahexacyclo[8.3.0.03,904,605,1307,11]tridecane: Two New C3-Symmetrical Oligocycles with Propeller Chirality.
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- Chemistry - A European Journal, 2005, v. 11, n. 7, p. 2012, doi. 10.1002/chem.200401027
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4,7,11-Triheterotrishomocubanes – Propeller-Shaped Highly Symmetrical Chiral Molecules Derived from BarreleneDedicated to Professor Paul von R. Schleyer on the occasion of his 75th birthday.
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- European Journal of Organic Chemistry, 2006, v. 2006, n. 11, p. 2590, doi. 10.1002/ejoc.200600019
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One-pot synthesis of polysaccharide 3,5-dimethylphenylcarbamates having a random vinyl group for immobilization on silica gel as chiral stationary phases.
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- Journal of Separation Science, 2006, v. 29, n. 10, p. 1432, doi. 10.1002/jssc.200600006
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High-performance liquid chromatographic enantioseparations on capillary columns containing crosslinked polysaccharide phenylcarbamate derivatives attached to monolithic silica.
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- Journal of Separation Science, 2006, v. 29, n. 13, p. 1988, doi. 10.1002/jssc.200500388
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Enantioseparation using alkoxyphenylcarbamates of cellulose and amylose as chiral stationary phase for high-performance liquid chromatography.
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- Journal of Separation Science, 2006, v. 29, n. 6, p. 915, doi. 10.1002/jssc.200500514
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High-performance liquid chromatographic enantioseparations on capillary columns containing monolithic silica modified with cellulose tris(3,5-dimethylphenylcarbamate).
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- Journal of Separation Science, 2004, v. 27, n. 10/11, p. 905, doi. 10.1002/jssc.200401819
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Separation of racemic compounds on amylose and cellulose dimethylphenylcarbamate-coated zirconia in HPLC.
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- Journal of Separation Science, 2003, v. 26, n. 15/16, p. 1331, doi. 10.1002/jssc.200301544
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Enantioseparations in capillary liquid chromatography and capillary electrochromatography using amylose tris(3,5-dimethylphenylcarbamate) in combination with aqueous organic mobile phase.
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- Journal of Separation Science, 2002, v. 25, n. 10/11, p. 653, doi. 10.1002/1615-9314(20020701)25:10/11<653::AID-JSSC653>3.0.CO;2-T
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Chromatographic enantioseparation on a wall-coated open tubular capillary column containing covalently bound cellulose (3,5-dichlorophenyl carbamate) as chiral selector.
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- Journal of Separation Science, 2002, v. 25, n. 3, p. 167, doi. 10.1002/1615-9314(20020201)25:3<167::AID-JSSC167>3.0.CO;2-8
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Enantioseparation by HPLC using phenylcarbonate, benzoylformate, p-toluenesulfonylcarbamate, and benzoylcarbamates of cellulose and amylose as chiral stationary phases.
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- Chirality, 2005, v. 17, n. 6, p. 299, doi. 10.1002/chir.20168
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Reversed-phase liquid chromatographic enantioseparation by cycloalkylcarboxylates of cellulose and amylose.
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- Chirality, 2004, v. 16, n. 5, p. 309
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Preparation of chiral stationary phase for HPLC based on immobilization of cellulose 3,5-dimethylphenylcarbamate derivatives on silica gel.
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- Chirality, 2003, v. 15, n. 1, p. 77, doi. 10.1002/chir.10169
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Chromatographic enantioseparation by cycloalkylcarbamate derivatives of cellulose and amylose.
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- Chirality, 2002, v. 14, n. 5, p. 372, doi. 10.1002/chir.10095
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Enantioseparation Using Cellulose Tris(3,5-dimethylphenylcarbamate) as Chiral Stationary Phase for HPLC: Influence of Molecular Weight of Cellulose.
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- Molecules, 2016, v. 21, n. 11, p. 1484, doi. 10.3390/molecules21111484
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