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Investigation on chiral capillary columns and their application in separation of enantiomers

Investigation on chiral capillary columns and their application in separation of enantiomers
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摘要 Six chiral diamide stationary phases (CSPs), namely N-(3-carbobenzoxypropionyl)-L- Val-tert-butylamide (CSP-1), N-undecenoyl-L-Val-S-α-phenylethylamide (CSP-2), N-undecenoyl-L- Val-R-α-phenylethylamide (CSP-3), OV-225-L-Val-tert-butylamide (CSP-4), XE-60-L-Val-tert- butylamide (CSP-5) and polycyanoethyl vinyl siloxane-L-Val-tert-butylamide (CSP-6), were inves- tigated and CSP-6 was crosslinked within narrow bore (70 μm) fused silica capillary columns. The separation of amino acid enantiomers on this narrow bore column by gas chromatography (GC) is illustrated. Six chiral diamide stationary phases (CSPs), namely N-(3-carbobenzoxypropionyl)-L- Val-tert-butylamide (CSP-1), N-undecenoyl-L-Val-S-α-phenylethylamide (CSP-2), N-undecenoyl-L- Val-R-α-phenylethylamide (CSP-3), OV-225-L-Val-tert-butylamide (CSP-4), XE-60-L-Val-tert- butylamide (CSP-5) and polycyanoethyl vinyl siloxane-L-Val-tert-butylamide (CSP-6), were inves- tigated and CSP-6 was crosslinked within narrow bore (70 μm) fused silica capillary columns. The separation of amino acid enantiomers on this narrow bore column by gas chromatography (GC) is illustrated.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 1992年第5期430-433,共0页 中国化学(英文版)
基金 the National Natural Science Foundation of China.
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