Sato Hirofumi, Shizuma Motohiro
Department of Biochemistry, Osaka Municipal Technical Research Institute, Japan.
J Oleo Sci. 2008;57(9):503-11. doi: 10.5650/jos.57.503.
The chiral-discriminating abilities of new triazole-linked host compounds (6, 7) toward amino acid esters were evaluated by the FABMS/EL-guest method. Two types of host appending saccharide derivatives were synthesized by the copper-catalyzed Huisgen-1,3-dipolar cycloaddition (CuAAC). Host compounds binding constants and chiral-discriminating abilities toward the enantiomeric alanine esters were evaluated by UV method in chloroform. The structural requirements of triazole-linked hosts were determined by their chiral-discriminating behaviors.
通过快原子轰击质谱/电喷雾电离-客体方法评估了新型三唑连接的主体化合物(6, 7)对氨基酸酯的手性识别能力。通过铜催化的胡伊斯根1,3-偶极环加成反应(CuAAC)合成了两类连接有糖类衍生物的主体。采用紫外法在氯仿中评估主体化合物对映体丙氨酸酯的结合常数和手性识别能力。通过其手性识别行为确定了三唑连接主体的结构要求。