本文报道15种新合成的2-硫-1,3,2-氧氮磷杂环戊烷衍生物的 EI 谱.在质量分析离子动能谱、碰撞诱导分解谱、B/E 联动扫描及高分辨精确质量测量的基础上,讨论了这类化合物的质谱裂解机理及特征.着重讨论上述化合物的氧硫异构现象及几种重...本文报道15种新合成的2-硫-1,3,2-氧氮磷杂环戊烷衍生物的 EI 谱.在质量分析离子动能谱、碰撞诱导分解谱、B/E 联动扫描及高分辨精确质量测量的基础上,讨论了这类化合物的质谱裂解机理及特征.着重讨论上述化合物的氧硫异构现象及几种重排反应.展开更多
Aim To develop a concise method for the synthesis of bicyclic azasugar and thiosugar with novel scaffold. Methods The two primary hydroxyl groups of compound 1 were selectively protected with tosyl cloloride in pyridi...Aim To develop a concise method for the synthesis of bicyclic azasugar and thiosugar with novel scaffold. Methods The two primary hydroxyl groups of compound 1 were selectively protected with tosyl cloloride in pyridine, followed by ring-closure with sodium sulfide or primary amine to form the oxy-bridged bicyclic molecules in good yields. Results Two bicyclic azasugars and a thiosugar were produced from L-sorbose in several steps. Conclusion The described procedures provide an efficient method to synthesize bicyclic azasugar and thiosugar with novel scaffold as potential glycosidase inhibitors.展开更多
基金We thank the National Science Foundation of China(NSFC,N0.20372003)for financial support.
文摘Aim To develop a concise method for the synthesis of bicyclic azasugar and thiosugar with novel scaffold. Methods The two primary hydroxyl groups of compound 1 were selectively protected with tosyl cloloride in pyridine, followed by ring-closure with sodium sulfide or primary amine to form the oxy-bridged bicyclic molecules in good yields. Results Two bicyclic azasugars and a thiosugar were produced from L-sorbose in several steps. Conclusion The described procedures provide an efficient method to synthesize bicyclic azasugar and thiosugar with novel scaffold as potential glycosidase inhibitors.
