Source:http://linkedlifedata.com/resource/pubmed/id/11405720
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2001-6-14
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pubmed:abstractText |
[see reaction]. The first example of a two-component chiral phase transfer catalyst is described which, operating in a biphasic solvent system, preferentially esterifies one enantiomer of a racemic N-acylated amino acid. The two-component catalyst is comprised of an achiral quaternary ammonium ion and a proline-derived chiral selector initially developed for the liquid chromatographic separation of enantiomers.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1523-7060
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
14
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pubmed:volume |
3
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1821-3
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pubmed:meshHeading | |
pubmed:year |
2001
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pubmed:articleTitle |
Two-component chiral phase transfer catalysts: enantioselective esterification of an N-acylated amino acid.
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pubmed:affiliation |
Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA. sesnyder@uiuc.edu
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pubmed:publicationType |
Journal Article
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