Catalytic intramolecular crossed aldehyde-ketone benzoin reactions: A novel synthesis of functionalized preanthraquinones

被引:173
作者
Hachisu, Y
Bode, JW
Suzuki, K
机构
[1] Tokyo Inst Technol, Dept Chem, Meguro Ku, Okayama, Tokyo 1528551, Japan
[2] Japan Sci & Technol Corp, CREST, Meguro Ku, Okayama, Tokyo 1528551, Japan
关键词
ANTIBIOTICS;
D O I
10.1021/ja035308f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Stereochemically and functionally rich polycyclic compounds are obtained by the first crossed aldehyde-ketone benzoin reaction in excellent yield under mild reaction conditions (5-20 mol % thiazolium salt, 10-70 mol % DBU, tBuOH, 40°C, 30 min). This novel catalytic methodology offers a convenient approach to sophisticated molecular architectures useful for the stereocontrolled construction of polycyclic compounds as well as the fully regiocontrolled synthesis of anthra- and naphthoquinones. Copyright © 2003 American Chemical Society.
引用
收藏
页码:8432 / 8433
页数:2
相关论文
共 27 条