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Volumn 1269, Issue , 2012, Pages 287-296

Mechanistic investigations of cinchona alkaloid-based zwitterionic chiral stationary phases

Author keywords

Amino acid; Aminosulfonic acid; Chiral stationary phase; Enantioseparation; Zwitterionic selector

Indexed keywords

APPLICATION RANGE; APROTIC; CHIRAL RECOGNITION; CHIRAL SELECTOR; CHIRAL STATIONARY PHASE; CHIRAL STATIONARY PHASIS; ELUTION ORDER; ENANTIOSEPARATIONS; ORGANIC MOBILE PHASIS; STRONG CATION EXCHANGES; STRUCTURAL MODIFICATIONS; SUBSTITUTION PATTERNS; TARGET ANALYTES; UNIQUE FEATURES; ZWITTERIONIC SELECTOR;

EID: 84870376290     PISSN: 00219673     EISSN: 18733778     Source Type: Journal    
DOI: 10.1016/j.chroma.2012.08.006     Document Type: Article
Times cited : (50)

References (36)
  • 31
    • 84871420905 scopus 로고    scopus 로고
    • Liquid chromatographic enantiomer separation and chiral recognition by cinchona alkaloid-derived enantioselective separation materials
    • CRC Press, Boca Raton, FL, N. Grinberg, E. Grushka (Eds.)
    • Lämmerhofer M., Lindner W. Liquid chromatographic enantiomer separation and chiral recognition by cinchona alkaloid-derived enantioselective separation materials. Advances in Chromatography 2007, CRC Press, Boca Raton, FL. N. Grinberg, E. Grushka (Eds.).
    • (2007) Advances in Chromatography
    • Lämmerhofer, M.1    Lindner, W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.