Chromatographic enantioseparation by cycloalkylcarbamate derivatives of cellulose and amylose

✍ Scribed by Takateru Kubota; Chiyo Yamamoto; Yoshio Okamoto

• Book ID: 102071863
• Publisher: John Wiley and Sons
• Year: 2002
• Tongue: English
• Weight: 92 KB
• Volume: 14
• Category: Article
• ISSN: 0899-0042
• DOI: 10.1002/chir.10095

✦ Synopsis

Abstract

Cyclopentyl and (±)‐exo‐2‐norbornylcarbamates of cellulose and amylose were prepared and their chiral recognition abilities as chiral stationary phases for high‐performance liquid chromatography (HPLC) were evaluated. Among these carbamates, cellulose tris(cyclopentylcarbamate) and amylose tris((±)‐exo‐2‐norbornylcarbamate) showed particularly high chiral recognition, which is comparable to that of several well‐known phenylcarbamate derivatives. The chiral recognition mechanism of cellulose tris(cyclohexylcarbamate), which was previously found to be an effective chiral stationary phase for HPLC, was investigated using NMR spectroscopy. The derivative dissolved in chloroform exhibited the chiral discrimination of several enantiomers in NMR as well as in HPLC. For example, the 1,1′‐bi‐2‐naphthol enantiomers were distinctly discriminated in the ^1^H, ^13^C, and 2D‐NOESY spectra. Chirality 14:372–376, 2002. © 2002 Wiley‐Liss, Inc.