摘要
寡聚α-尿嘧啶核苷酸具有阻止蛋白酶非专一性降解的功能.研究了合成寡聚α-尿嘧啶核苷酸的重要中间体5′-氧-双对甲氧基三苯甲基-α-尿嘧啶核苷的新方法,比文献报道的产率有所提高,由文献的66%提高到85%.
α Anomeric oligouridylates are possessed of resistancet to non specific degradation by nucleases.A new method for the preparation of the key intermediate 5′ O dimethoxytrityl α uridine in synthesis of α anomeric oligouridylates was studied in this paper.The yield of the new method was higher than that the literature had reported.
出处
《中国药物化学杂志》
CAS
CSCD
1997年第1期63-65,共3页
Chinese Journal of Medicinal Chemistry
关键词
药物
双对甲氧基
三苯甲基
尿嘧啶核苷
合成
5'-O-dimethoxytritylαuridine
5-O-dimethoxytrityl 2,2-anhydro 1-α-D ribo-furanosyluracil
synthesis