About: Direct resolution of optically active isomers on chiral packings containing ergoline skeleton. 6. Enantioseparation of profens

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About: Direct resolution of optically active isomers on chiral packings containing ergoline skeleton. 6. Enantioseparation of profens Goto Sponge NotDistinct Permalink

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scientific article published on 01 January 1999

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rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в січні 1999 (uk) im Januar 1999 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xineru de 1999 (ast) artikull shkencor i botuar më 01 janar 1999 (sq) scientific article published on 01 January 1999 (en)
publication date	wds:Q77389823-550E20E0-7C0A-4F5B-B965-EECBF1741783
publication date	1999-01-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q77389823-0B084BF8-C9EE-41D1-B3CD-BDE921F1ADFE wds:Q77389823-101E6461-18D1-4B65-ABB7-37B47DBCBBCE wds:Q77389823-2B49A695-3A65-4CB6-A2EA-33B497513068 wds:Q77389823-2D7789E7-3FFC-4183-901C-3577CFE886BE wds:Q77389823-2FABCD92-0E3B-4F73-B00B-B0C1F0DCE669 wds:Q77389823-5798A761-0945-40E0-B2E4-A1591C414338 wds:Q77389823-6AFBE6EF-6C13-4DE5-B579-BB48FE30D657 wds:Q77389823-7F760973-716A-4E63-83FD-77CC060E04A1 wds:Q77389823-A419295A-1C2E-4CC5-A1AD-404BAD98415A wds:Q77389823-DB4E5449-E279-45FE-BD44-4A8B540A9CD8 wds:Q77389823-E12F77E8-F27A-4EC3-8C29-1A6A37379DF2 wds:Q77389823-E2ACE276-93E3-4486-9A77-8AC22D5A2001 wds:Q77389823-EA5830C3-2C73-45E4-9115-92BEABF15E38 wds:Q77389823-F1F64C73-AE61-4C5C-AAC7-F0A3B99B6C66
cites work	Separation of drug stereoisomers by the formation of beta-cyclodextrin inclusion complexes Application of an ovomucoid-conjugated column for the optical resolution of some pharmaceutically important compounds Pharmacological differences between the optical isomers of ibuprofen: evidence for metabolic inversion of the (—)-isomer The metabolic chiral inversion of 2-arylpropionic acids—a novel route with pharmacological consequences Enantioselective pharmacodynamics of the nonsteroidal antiinflammatory drug ketoprofen: in vitro inhibition of human platelet cyclooxygenase activity Formation of glycine conjugate and (-)-(R)-enantiomer from (+)-(S)-2-phenylpropionic acid suggesting the formation of the CoA thioester intermediate of (+)-(S)-enantiomer in dogs Stereospecific high-performance liquid chromatographic assay of ibuprofen: improved sensitivity and sample processing efficiency Microbial metabolism of 2-arylpropionic acids: chiral inversion of ibuprofen and 2-phenylpropionic acid Pharmacokinetics of ibuprofen enantiomers in dogs Direct resolution of optically active isomers on chiral packings containing ergoline skeletons. 5. Enantioseparation of amino Acid derivatives A nuclear magnetic resonance study of the diastereoisomer complexes formed between a terguride derivative and naproxen Pulmonary inversion of 2-arylpropionic acids: influence of protein binding Simultaneous determination of furprofen and rufloxacin in human plasma by high-performance liquid chromatography Displacement chromatography on cyclodextrin silicas. IV. Separation of the enantiomers of ibuprofen
author name string	wds:Q77389823-011BBF89-239F-4C34-A043-AE42085B70EB wds:Q77389823-43A33C2B-39C9-43AD-AB8A-CFDA5F6A122E wds:Q77389823-53F66DF7-013C-4845-8819-966AEACD3834 wds:Q77389823-F34FD119-5DA6-486E-92D4-E0D4E416689F wds:Q77389823-F3B1C8DF-FC89-4E05-8289-4D3F994E73A3
author name string	Flieger M Olsovská J Messina A Bachechi F Sinibaldi M
rdfs:label	Direct resolution of optically active isomers on chiral packings containing ergoline skeleton. 6. Enantioseparation of profens (en) Direct resolution of optically active isomers on chiral packings containing ergoline skeleton. 6. Enantioseparation of profens (nl) Direct resolution of optically active isomers on chiral packings containing ergoline skeleton. 6. Enantioseparation of profens (sq)
skos:prefLabel	Direct resolution of optically active isomers on chiral packings containing ergoline skeleton. 6. Enantioseparation of profens (en) Direct resolution of optically active isomers on chiral packings containing ergoline skeleton. 6. Enantioseparation of profens (nl) Direct resolution of optically active isomers on chiral packings containing ergoline skeleton. 6. Enantioseparation of profens (sq)
name	Direct resolution of optically active isomers on chiral packings containing ergoline skeleton. 6. Enantioseparation of profens (en) Direct resolution of optically active isomers on chiral packings containing ergoline skeleton. 6. Enantioseparation of profens (nl) Direct resolution of optically active isomers on chiral packings containing ergoline skeleton. 6. Enantioseparation of profens (sq)
title	wds:Q77389823-6FDE9C02-58BA-465F-AF92-7EF63EFDADBB
title	Direct resolution of optically active isomers on chiral packings containing ergoline skeleton. 6. Enantioseparation of profens (en)
page(s)	wds:Q77389823-A95CD825-4DB9-418A-A4E8-085924AA49BD
page(s)	291-300
instance of	wds:Q77389823-2A9B329D-0DA5-4C8B-80EE-B0190EE12243
instance of	scholarly article
main subject	wds:Q77389823-BD657CDE-C102-4CE5-B2BE-CADC98968872
main subject	chirality
PubMed ID	wds:Q77389823-28D05396-4C6A-43D2-9B20-DE17A69FF4D4
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10224656
PubMed ID	10224656
published in	wds:Q77389823-A6FD1CAD-1CEA-44DA-9118-9D44ACBE4495
published in	Chirality
issue	wds:Q77389823-B1EE507A-D9F4-4573-B667-52A36F2AD0B9
volume	wds:Q77389823-124A897C-9719-4471-8FCC-2409B44D39B2
issue	4
volume	11
DOI	wds:Q77389823-A8AA167D-D573-42FC-88FA-63B93D56B8D0
DOI	http://dx.doi.org/10.1002/(SICI)1520-636X(1999)11:4%3C291::AID-CHIR6%3E3.0.CO;2-4
DOI	10.1002/(SICI)1520-636X(1999)11:4<291::AID-CHIR6>3.0.CO;2-4
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q77389823
is cites work of	Separation of enantiomers: needs, challenges, perspectives. Novel cinchona alkaloid carbamate C9-dimers as chiral anion-exchange type selectors for high-performance liquid chromatography Enantiomeric separation of R,S-naproxen by conventional and nano-liquid chromatography with methyl-beta-cyclodextrin as a mobile phase additive High-performance liquid chromatography chiral stationary phases based on low-molecular-mass selectors. High-performance liquid chromatography study of the enantiomer separation of chrysanthemic acid and its analogous compounds on a terguride-based stationary phase. CEC enantioseparations of carboxylic acids on silica-based monoliths modified with ergot alkaloid derivative.
is cites work of	wds:Q73555992-555D03D1-BFDB-46E7-8E1E-8299529CA1B8 wds:Q34160381-DD3141DD-3366-4FEA-8D24-0141D397166C wds:Q34160395-B8008058-4280-411D-A3A5-62CC740B1FD6 wds:Q43719153-47FB7D0C-5DD1-41FF-B7BC-E74434BD70A5 wds:Q43289825-F87BE9E8-E64F-47BA-BA25-91BD3793DFB4 wds:Q52574591-573ACF78-7E5A-489E-B49D-8EDDBA7F9D96

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