摘要
报道了一条合成丁烷木脂素的新路线.以芳香醛为起始原料,Stobbe缩合和烷基化反应为关键步骤,构建了木脂素骨架,再经拆分及还原,可得到相应的苏式和赤式异构体.经官能团转化得到5个丁烷木脂素和8个丁醚木脂素,其中3个天然产物为首次合成.对合成产物进行抗HIV病毒和和抗疱疹病毒活性研究,部分化合物显示出较高的抗病毒活性,而且骨架构型对活性影响较大.
Liguans are widely distributed in the plant kingdom. Among liguans, many dibenzylbutane lignans and their analogues exhibit a strong bioactivity. A novel synthetic route to dibenzylbutane lignans using simple aldehydes as the starting materials is described. The method involves Stobbe Condensation and condensation of aromatic aldehyde and alkylation to give the complete skeleton of lignans. Then, by the resolution of （ - ） -diacid, a simple separation of threo- and erythro-isomers and structural modification, the target materials were obtained. Five dibenzylbutane lignans and eight dibenzylbutyl ether lignans were synthesized. Bioactivity results indicate that some compounds showed better activities against the HIV and herpes virus, and bioaetivity is greatly affected by the skeleton configuration.
出处
《高等学校化学学报》
SCIE
EI
CAS
CSCD
北大核心
2008年第11期2178-2182,共5页
Chemical Journal of Chinese Universities
基金
山东省自然科学基金(批准号:Q2006B02)
兰州大学功能有机分子国家重点实验室开放基金(批准号:200708)资助
