Cyclodextrins as chiral stationary phases in capillary gas chromatography. Part VII: Cyclodextrins with an inverse substitution pattern – synthesis and enantioselectivity

Abstract

Abstract Transferring the site of specific substitution of dipentylated cyclodextrins with methyl or acyl residues from the secondary 3‐hydroxyl group to the primary 6‐hydroxyl group was expected to provide new information on the mechanism of chiral recognition. The 3‐position points towards and the 6‐position points away from the cyclodextrin cavity which via inclusion complex formation is supposed to play a major role in chiral separation. The “inverse” 6‐O‐acyl‐2,3‐di‐O‐pentyl‐cyclodextrins displayed almost no enantioselectivity but the corresponding 6‐O‐methyl derivatives are a versatile supplement to the chiral capillary GC phases nowadays available. Among the compounds that could be enantiomerically resolved are alcohols, amino acids, alkyl halides, bicyclic ethers, acetals, olefins, other hydrocarbons and chiral pharmaceuticals.