about
Expanding the potential of chiral chromatography for high-throughput screening of large compound libraries by means of sub-2μm Whelk-O 1 stationary phase in supercritical fluid conditions.Recent advancements and future directions of superficially porous chiral stationary phases for ultrafast high-performance enantioseparations.Rationale behind the optimum efficiency of columns packed with new 1.9μm fully porous particles of narrow particle size distribution.Experimental evidence of the kinetic performance achievable with columns packed with new 1.9μm fully porous particles of narrow particle size distribution.Ultra-fast high-efficiency enantioseparations by means of a teicoplanin-based chiral stationary phase made on sub-2 μm totally porous silica particles of narrow size distribution.Cannabis through the looking glass: chemo- and enantio-selective separation of phytocannabinoids by enantioselective ultra high performance supercritical fluid chromatography.Evaluation of two sub-2μm stationary phases, core–shell and totally porous monodisperse, in the second dimension of on-line comprehensive two dimensional liquid chromatography, a case study: Separation of milk peptides after expiration dateOn the effect of chiral selector loading and mobile phase composition on adsorption properties of latest generation fully- and superficially-porous Whelk-O1 particles for high-efficient ultrafast enantioseparationsDirect analysis of chiral active pharmaceutical ingredients and their counterions by ultra high performance liquid chromatography with macrocyclic glycopeptide-based chiral stationary phasesPirkle-type chiral stationary phase on core–shell and fully porous particles: Are superficially porous particles always the better choice toward ultrafast high-performance enantioseparations?Unmatched Kinetic Performance in Enantioselective Supercritical Fluid Chromatography by Combining Latest Generation Whelk-O1 Chiral Stationary Phases with a Low-Dispersion in-House Modified EquipmentSimultaneous Preconcentration, Identification, and Quantitation of Selenoamino Acids in Oils by Enantioselective High Performance Liquid Chromatography and Mass Spectrometry
P50
Q35554958-8CB620F8-80BF-442F-8280-6D112B33D7F1Q38770043-E46DEA46-B5E5-4E63-AE1A-9209F4707567Q47298687-61DCCC48-BCA5-4022-A030-991DD04251CEQ47300626-126F8E44-8A6A-4030-959A-1E3BACB0DA7DQ47338727-1FAFF4A9-105D-4B5F-8F21-522C31877555Q50089022-8FF16A53-C35D-4BF1-9711-2363DE6D273EQ58960661-87EBFF25-A000-4D71-901F-6AA4C18A69B0Q60712037-686705F5-61DB-46CA-B1EA-8179F4D12040Q60712039-DB05E4F6-D945-4AA2-9896-2A6B03243F68Q60712052-EF786046-6182-4AF5-B2ED-95BB8A664933Q60719744-82241098-DFD4-4B3C-8E78-2F40741DB29FQ89127591-64ABA0ED-E211-486C-B0D0-65D4C9C7EA7F
P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0003-0970-2917
@en
name
Omar Ismail
@ast
Omar Ismail
@en
Omar Ismail
@es
Omar Ismail
@nl
type
label
Omar Ismail
@ast
Omar Ismail
@en
Omar Ismail
@es
Omar Ismail
@nl
prefLabel
Omar Ismail
@ast
Omar Ismail
@en
Omar Ismail
@es
Omar Ismail
@nl
P106
P1153
56450453900
P21
P31
P496
0000-0003-0970-2917