Published in J Sep Sci on June 01, 2007
Facile synthesis of mono-6-amino-6-deoxy-alpha-, beta-, gamma-cyclodextrin hydrochlorides for molecular recognition, chiral separation and drug delivery. Nat Protoc (2008) 1.06
Preparation and chiral recognition of a novel chiral stationary phase for high-performance liquid chromatography, based on mono(6A-N-allylamino-6A-deoxy)-perfunctionalized beta-cyclodextrin and covalently bonded silica gel. J Chromatogr A (2004) 0.92
Synthesis and application of single-isomer 6-mono(alkylimidazolium)-beta-cyclodextrins as chiral selectors in chiral capillary electrophoresis. Electrophoresis (2005) 0.82
Synthesis and chromatographic properties of a novel chiral stationary phase derived from heptakis(6-azido-6-deoxy-2,3-di-O-phenylcarbamoylated)-beta-cyclodextrin immobilized onto amino-functionalized silica gel via multiple urea linkages. J Chromatogr A (2002) 0.82
Chiral capillary electrophoresis with cationic pyrrolidinium-beta-cyclodextrin derivatives as chiral selectors. J Sep Sci (2010) 0.81
"Click" preparation of hindered cyclodextrin chiral stationary phases and their efficient resolution in high performance liquid chromatography. J Chromatogr A (2010) 0.81
Monosubstituted positively charged cyclodextrins: Synthesis and applications in chiral separation. J Sep Sci (2008) 0.81
Enantioseparation of a novel "click" chemistry derived native beta-cyclodextrin chiral stationary phase for high-performance liquid chromatography. J Chromatogr A (2009) 0.81
Cationic cyclodextrins chemically-bonded chiral stationary phases for high-performance liquid chromatography. Anal Chim Acta (2012) 0.80
"Click" immobilized perphenylcarbamated and permethylated cyclodextrin stationary phases for chiral high-performance liquid chromatography application. J Chromatogr A (2010) 0.79
Hydroxyethylammonium monosubstituted cyclodextrin as chiral selector for capillary electrophoresis. Anal Chim Acta (2013) 0.79
Recent development of cyclodextrin chiral stationary phases and their applications in chromatography. J Chromatogr A (2012) 0.79
Synthesis of cationic beta-cyclodextrin derivatives and their applications as chiral stationary phases for high-performance liquid chromatography and supercritical fluid chromatography. J Chromatogr A (2008) 0.78
Urea bonded cyclodextrin derivatives onto silica for chiral HPLC. J Sep Sci (2006) 0.78
Sub-2 μm porous silica materials for enhanced separation performance in liquid chromatography. J Chromatogr A (2011) 0.78
Novel β-cyclodextrin chiral stationary phases with different length spacers for normal-phase high performance liquid chromatography enantioseparation. J Chromatogr A (2011) 0.77
Synthesis and application of mono-6-(3-methylimidazolium)-6-deoxyperphenylcarbamoyl-beta-cyclodextrin chloride as chiral stationary phases for high-performance liquid chromatography and supercritical fluid chromatography. J Chromatogr A (2008) 0.77
Development of in-tube solid-phase microextraction coupled to pressure-assisted CEC and its application to the analysis of propranolol enantiomers in human urine. Electrophoresis (2007) 0.75
Preparation and enantioseparation characteristics of two chiral stationary phases based on mono(6(A)-azido-6(A)-deoxy)-perphenylcarbamoylated alpha- and gamma-cyclodextrin. Chirality (2004) 0.75
Enantioseparation on mono(6A-n-allylamino-6A-deoxy)permethylated 3-cyclodextrin covalently bonded silica gel. J Chromatogr A (2004) 0.75
Chemically bonded cationic β-cyclodextrin derivatives and their applications in supercritical fluid chromatography. J Chromatogr A (2011) 0.75
Enantioseparation of acidic enantiomers in capillary electrophoresis using a novel single-isomer of positively charged beta-cyclodextrin: Mono-6A-N-pentylammonium-6A-deoxy- beta-cyclodextrin chloride. J Chromatogr A (2005) 0.75
Synthesis and application of a novel single-isomer mono-6-deoxy-6-(3R,4R-dihydroxypyrrolidine)-beta-cyclodextrin chloride as a chiral selector in capillary electrophoresis. J Chromatogr A (2008) 0.75
Chromatographic evaluation and comparison of three beta-cyclodextrin-based stationary phases by capillary liquid chromatography and pressure-assisted capillary electrochromatography. Electrophoresis (2008) 0.75
Novel cyclodextrin chiral stationary phases for high performance liquid chromatography enantioseparation: effect of cyclodextrin type. J Chromatogr A (2011) 0.75
Perphenylcarbamoylated beta-cyclodextrin bonded-silica particles as chiral stationary phase for enantioseparation by pressure-assisted capillary electrochromatography. Electrophoresis (2006) 0.75
Enantioselective separation of dansyl-DL-amino acids and some racemates on "click" functionalized native α-cyclodextrin based sub-2 μm columns. Analyst (2013) 0.75
Synthesis of cationic single-isomer cyclodextrins for the chiral separation of amino acids and anionic pharmaceuticals. Nat Protoc (2007) 0.75
Enantioselectively controlled release of chiral drug (metoprolol) using chiral mesoporous silica materials. Nanotechnology (2010) 0.75
Monodispersed submicron porous silica particles functionalized with CD derivatives for chiral CEC. Electrophoresis (2010) 0.75
Synthesis of large pore-diameter SBA-15 mesostructured spherical silica and its application in ultra-high-performance liquid chromatography. J Chromatogr A (2009) 0.75
Application of Click-chemistry-based perphenylcarbamated beta-CD chiral stationary phase in CEC. Electrophoresis (2009) 0.75
Sub-1-micron mesoporous silica particles functionalized with cyclodextrin derivative for rapid enantioseparations on ultra-high pressure liquid chromatography. J Chromatogr A (2010) 0.75
Enantioseparation of dansyl amino acids by ultra-high pressure liquid chromatography using cationic β-cyclodextrins as chiral additives. Analyst (2011) 0.75
A family of single-isomer positively charged cyclodextrins as chiral selectors for capillary electrophoresis: mono-6A-butylammonium-6A-deoxy-beta-cyclodextrin tosylate. Electrophoresis (2005) 0.75
Synthesis and application of mono-2A-azido-2A-deoxyperphenylcarbamoylated beta-cyclodextrin and mono-2A-azido-2A-deoxyperacetylated beta-cyclodextrin as chiral stationary phases for high-performance liquid chromatography. J Chromatogr A (2005) 0.75