摘要
着重对具有抗癌活性的甲酰胺基噻唑 C-核苷 (Tiazofurin)类化合物的分子结构特点作了系列分析 ,提出以异口恶唑烷 (啉 )基环取代现有呋喃核糖环合成新型抗病毒活性的甲酰胺基噻唑
Efforts have been made in analysis of structural modification of Tiazofurin C\|nucleoside analogues and in attempting to find the structure\|activity relationship of those analogs.To find high antitumor activty C\|nucleosides,one class of Tiazofurin C\|nucleoside analogues in which the ribofuranosyl sugar is replaced by novel isoxazolidinyl (isoxazolinyl) rings has been designed.Some reasonable synthesis schemes have been considered.
出处
《光谱实验室》
CAS
CSCD
2001年第5期568-574,共7页
Chinese Journal of Spectroscopy Laboratory