|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
1
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pubmed:dateCreated |
1997-2-5
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|
pubmed:abstractText |
A cyclodextrin-modified micellar capillary electrophoretic method was developed for the chiral separation of 2-methyltaurine. The racemic mixture was separated after derivatization with dansyl chloride. The enantiomeric separation of the dansyl derivative was done using electrolyte solutions containing beta-cyclodextrin (beta-CD) or different ratios of beta- and gamma-CD. The mixture of beta- and gamma-CD optimally resolved the compound studied.
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pubmed:language |
eng
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pubmed:journal |
|
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pubmed:citationSubset |
IM
|
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pubmed:chemical |
|
|
pubmed:status |
MEDLINE
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pubmed:month |
May
|
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pubmed:issn |
1572-6495
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pubmed:author |
|
|
pubmed:issnType |
Print
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|
pubmed:day |
31
|
|
pubmed:volume |
681
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
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pubmed:pagination |
83-6
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pubmed:dateRevised |
2007-10-16
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|
pubmed:meshHeading |
|
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pubmed:year |
1996
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|
pubmed:articleTitle |
Chiral resolution of the dansyl derivative of 2-methyltaurine by capillary electrophoresis.
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pubmed:affiliation |
Dipartimento di Scienze Farmaceutiche, Università di Modena, Italy.
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|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
