Oxygen insertion in Sesamum indicum furanofuran lignans. Diastereoselective syntheses of enzyme substrate analogues

被引:21
作者
Marchand, PA
Zajicek, J
Lewis, NG
机构
[1] WASHINGTON STATE UNIV,INST BIOL CHEM,PULLMAN,WA 99164
[2] UNIV NOTRE DAME,DEPT CHEM & BIOCHEM,NOTRE DAME,IN 46556
来源
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE | 1997年 / 75卷 / 06期
关键词
furofuran lignans; sesame; epimers; salicifoliol; acuminatolide;
D O I
10.1139/v97-102
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The furofuran lignans in sesame seed have an unusual oxygen insertion between their furan and aryl rings. In our continuing investigations on the isolation and characterization of the enzyme(s) involved, the diastereoselective syntheses of various substrate analogues for the oxygen insertion step were developed for future substrate specificity and inhibitor studies. This synthetic strategy also provided entry to so-called furofuranone epoxy-lignans, such as salicifoliol from Bupleurum sp., and acuminatolide from Helichrysum sp.
引用
收藏
页码:840 / 849
页数:10
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