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Volumn 1269, Issue , 2012, Pages 297-307

Versatility of cinchona-based zwitterionic chiral stationary phases: Enantiomer and diastereomer separations of non-protected oligopeptides utilizing a multi-modal chiral recognition mechanism

Author keywords

Chiral stationary phase; HPLC; Ion exchange; Peptide; Sequence isomers; Stereoisomer separation

Indexed keywords

ALIPHATIC SIDE CHAIN; AMIDE GROUPS; AROMATIC SIDE CHAINS; BENZYL GROUP; CARBAMOYL; CATION EXCHANGERS; CHIRAL RECOGNITION MECHANISMS; CHIRAL SELECTOR; CHIRAL STATIONARY PHASE; CHIRAL STATIONARY PHASIS; CINCHONA ALKALOID; DIASTEREOMERS; ENANTIOMER SEPARATION; FLEXIBLE SPACER; HOMOCHIRAL; HPLC; MOBILE PHASE CONDITIONS; MULTI-MODAL; OLIGOPEPTIDES; PEPTIDE BACKBONES; RETENTION FACTORS; SEQUENCE ISOMERS; STRUCTURAL FEATURE; SULFONIC ACID; ZWITTERION FORMATION;

EID: 84870379858     PISSN: 00219673     EISSN: 18733778     Source Type: Journal    
DOI: 10.1016/j.chroma.2012.06.094     Document Type: Article
Times cited : (25)

References (35)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.