Natalini B, Sardella R, Macchiarulo A, Pellicciari R
Università degli Studi di Perugia, Dipartimento di Chimica e Tecnologia del Farmaco, Perugia, Italy.
Chirality. 2006 Aug;18(7):509-18. doi: 10.1002/chir.20280.
S-benzyl-(R)-cysteine (R-SBC) is a new chiral ligand-exchange stationary phase which has proved to be effective in the analytical separation of some natural and unnatural underivatized amino acids with fair to good separation and resolution factors. The dynamic coating of the RP-18 solid support with S-Benzyl-(R)-cysteine (R-SBC) gives rise to a stable and efficient chiral stationary phase (CSP) that has been successfully employed. The mechanism of chiral recognition is discussed and a molecular modeling study aimed at identifying molecular descriptors responsible for observed different behaviours of analytes upon different albeit closely related selectors is discussed.
S-苄基-(R)-半胱氨酸(R-SBC)是一种新型手性配体交换固定相,已证明其在分析分离一些天然和非天然未衍生化氨基酸方面有效,具有相当好至良好的分离度和分辨率因子。用S-苄基-(R)-半胱氨酸(R-SBC)对RP-18固体载体进行动态涂覆,可产生一种已成功应用的稳定且高效的手性固定相(CSP)。文中讨论了手性识别机制,并探讨了一项分子建模研究,该研究旨在确定导致分析物在不同但密切相关的选择剂上表现出不同行为的分子描述符。