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Digitale Medien

A chiral stationary phase which affords unusually high levels of enantioselectivity (1991)

Pirkle, William H. ; Deming, Kris C. ; Burke, John A.

New York, NY [u.a.] : Wiley-Blackwell

Chirality 3 (1991), S. 183-187

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Details

ISSN: 0899-0042

Schlagwort(e): (S)-N-(1-naphthyl)leucine ; N-(3,5-dinitrobenzoyl) ; amino acids ; derivatives ; 3,5-dinitroanilides of chiral acids ; Chemistry ; Organic Chemistry

Quelle: Wiley InterScience Backfile Collection 1832-2000

Thema: Chemie und Pharmazie

Notizen: A chiral stationary phase (CSP) derived from N-(1-naphthyl) leucine has been prepared. This CSP is conceptually similar to the CSP derived from N-(2-naphthyl)alanine and was expected to separate the enantiomers of the same clientele of analytes as does the latter. The magnitudes of the separation factors observed on the two CSPs may differ markedly for a given analyte, the new CSP often affording much greater enantioselectivity.

Zusätzliches Material: 3 Tab.

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1002/chir.530030308

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