摘要
以全乙酰化的2-叠氮基半乳糖基三氯乙酰亚胺酯为起始原料,通过与L-苏氨酸衍生物的糖基化反应以及叠氮还原,并同时进行N-乙酰化的一锅法反应制得全保护的Tn抗原,在脱去苏氨酸上的氨基保护基后,含生物素的琥珀酰亚胺酯与Tn抗原上的氨基发生选择性胺解得到标题化合物。目标产物及重要中间体的结构都通过1HNMR、13CNMR和MS进行了表征。
Through the glycosylation reaction between the fully acetylated 2-azido-galactosyltrichloroacetimidate and L-threonine derivative,followed by azido-teduction and N-acetylation in one pot the fully protected Tn antigen was obtained. After deprotection of amino group on threonine, amino-attached Tn antigen was lig- ated selectively with suecinimidyl ester containing biotin to afford the biotin-labeled tin antigen. The structures of desired product and key internaediates were characterized by ^1HNMR, ^13CNMR and MS.
出处
《化学试剂》
CAS
CSCD
北大核心
2009年第5期334-336,361,共4页
Chemical Reagents
关键词
Tn抗原
生物素
糖基化反应
合成
Tn antigen
botin
glycosylation reaction
synthesis