About: Non-aqueous capillary electrophoretic enantioseparation of N-derivatized amino acids using cinchona alkaloids and derivatives as chiral counter-ions

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About: Non-aqueous capillary electrophoretic enantioseparation of N-derivatized amino acids using cinchona alkaloids and derivatives as chiral counter-ions Goto Sponge Distinct Permalink

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scientific article published on 01 April 2000

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) wüsseschaftlicher Artikel, wo im April 2000 veröffentlicht worden isch (gsw) наукова стаття, опублікована у квітні 2000 (uk) im April 2000 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'abril de 2000 (ast) scientific article published on 01 April 2000 (en)
publication date	wds:Q73853270-C9357922-3255-475E-B0BB-647204CEBC45
publication date	2000-04-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q73853270-690BECAF-BD95-4A49-A554-A3A0DAC8E769
language of work or name	English
cites work	wds:Q73853270-23911FF9-7E4F-4209-A7CB-35551F646E53 wds:Q73853270-865CA28B-57E7-4EDD-AB25-7CFF2D35CA09 wds:Q73853270-B1E58098-09E4-427E-A9FD-C586E8F63EF4 wds:Q73853270-E6A52DFC-52D6-4D1A-91A5-6159C7B7143A
cites work	Separation and detection of amino acids and their enantiomers by capillary electrophoresis: a review Enantiomeric separation of N-protected amino acids by non-aqueous capillary electrophoresis using quinine or tert-butyl carbamoylated quinine as chiral additive Computerized optimization of the high-performance liquid chromatographic enantioseparation of a mixture of 4-dinitrophenyl amino acids on a quinine carbamate-type chiral stationary phase using DRYLAB Chiral separations by capillary zone electrophoresis: present state of the art.
author name string	wds:Q73853270-1CAD9022-1FA1-4E39-AECA-62B1F14F071C wds:Q73853270-8D98107D-9745-4FBE-B838-5957E3823529 wds:Q73853270-E7854B37-80F8-436A-8F02-CC3DE496491A
author name string	J Crommen W Lindner V Piette
rdfs:label	Non-aqueous capillary electrophoretic enantioseparation of N-derivatized amino acids using cinchona alkaloids and derivatives as chiral counter-ions (en) Non-aqueous capillary electrophoretic enantioseparation of N-derivatized amino acids using cinchona alkaloids and derivatives as chiral counter-ions (nl)
skos:prefLabel	Non-aqueous capillary electrophoretic enantioseparation of N-derivatized amino acids using cinchona alkaloids and derivatives as chiral counter-ions (en) Non-aqueous capillary electrophoretic enantioseparation of N-derivatized amino acids using cinchona alkaloids and derivatives as chiral counter-ions (nl)
name	Non-aqueous capillary electrophoretic enantioseparation of N-derivatized amino acids using cinchona alkaloids and derivatives as chiral counter-ions (en) Non-aqueous capillary electrophoretic enantioseparation of N-derivatized amino acids using cinchona alkaloids and derivatives as chiral counter-ions (nl)
author	wds:Q73853270-F7669F47-5818-432E-B059-D595C51B52D8
author	Marianne Fillet
title	wds:Q73853270-2E840832-D697-44DC-97DC-19AFC868BBB3
title	Non-aqueous capillary electrophoretic enantioseparation of N-derivatized amino acids using cinchona alkaloids and derivatives as chiral counter-ions (en)
page(s)	wds:Q73853270-DFFD62BE-53B8-47E4-80CC-54A4BE9CEC29
page(s)	353-360
instance of	wds:Q73853270-F202F283-44DB-43B0-8F37-44F78C4563B4
instance of	scholarly article
main subject	wds:Q73853270-91915321-BEF4-4296-AB4A-A4CF86A2A80C
main subject	chirality
PubMed ID	wds:Q73853270-05711CA0-583D-48DC-A439-3B9AAA516FC4
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10839155
PubMed ID	10839155
published in	wds:Q73853270-C73CD0B9-2EED-4279-BCF0-F13813A3118E
published in	Journal of Chromatography
issue	wds:Q73853270-926A348D-90C2-4187-9D77-11CE2F5BA2AE
volume	wds:Q73853270-8A2A8096-F1EB-4328-9E47-7701D3935B6B
issue	1-2
volume	875
DOI	wds:Q73853270-F5C60BF1-9853-4B59-9130-20CD76F1C439
DOI	http://dx.doi.org/10.1016/S0021-9673(00)00083-2
DOI	10.1016/S0021-9673(00)00083-2
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73853270
is cites work of	Enantioseparation of anionic analytes by non-aqueous capillary electrophoresis using quinine and quinidine derivatives as chiral counter-ions Fundamental aspects of chiral separations by capillary electrophoresis Chiral separations by capillary electrophoresis: Recent developments and applications Selected fundamental aspects of chiral electromigration techniques and their application to pharmaceutical and biomedical analysis Enantioseparations using capillary electromigration techniques in nonaqueous buffers Enantioseparations in capillary electromigration techniques: recent developments and future trends Recent developments in chiral capillary electrophoresis and applications of this technique to pharmaceutical and biomedical analysis Advances in chiral separations by nonaqueous capillary electrophoresis in pharmaceutical and biomedical analysis Separation of propranolol enantiomers by CE using sulfated beta-CD derivatives in aqueous and non-aqueous electrolytes: comparative CE and NMR study. Recent advances in amino acid analysis by capillary electrophoresis Sensitive chiral analysis by capillary electrophoresis Enantiomeric separation of N-protected amino acids by non-aqueous capillary electrophoresis with dimeric forms of quinine and quinidine derivatives serving as chiral selectors Enantiomer separation of N-protected amino acids by non-aqueous capillary electrophoresis and high-performance liquid chromatography with tert.-butyl carbamoylated quinine in either the background electrolyte or the stationary phase Some thoughts about enantioseparations in capillary electrophoresis Evaluation of the contribution to enantioselectivity of quinine and quinidine scaffolds in chemically and physically mixed chiral selectors Development of stereoselective nonaqueous capillary electrophoresis system for the resolution of cationic and amphoteric analytes
is cites work of	wds:Q34393734-8936B9AB-272C-4F88-8D75-42A48284DFA3 wds:Q77587459-819F421D-232C-43D6-98C6-1B0F3F61903B wds:Q91969945-DA62155A-BCA8-4E5B-9D07-F4A82353EEAD wds:Q36372073-B12400D4-F2AA-4085-BB79-5ACA9E95B70E wds:Q43563247-801E149B-3489-41C7-8E42-F48E02C367FA wds:Q34470029-7A2424ED-7025-4523-A35B-F9D722444FA0 wds:Q36475116-4D917354-082A-4232-A1FE-E06578B3DB7A wds:Q34393726-D839FEA2-D48A-4257-B1D3-6E14C9F1999F wds:Q44338973-4C8CE370-FB6F-4F9D-96DB-F4FB6A5A8CDB wds:Q43758335-A7F68AF4-B0F3-4F00-8DAF-792DA152A912 wds:Q73254475-3E896E39-8A99-49A8-B841-D8AF1FA80971 wds:Q33548396-5819EDDC-0AF5-412D-83D9-368B76B67BF9 wds:Q34160390-79CF8156-9390-4BD6-950C-79FEDC39A52E wds:Q34147242-50A6CE1B-89E8-4D1E-B267-B01AB8B6625E wds:Q38126456-629349D6-E0B3-4A01-A0BC-E77BE1E9AF3D wds:Q44494486-C5B940FD-854A-4E65-94BC-9FBBEB82D5CA

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