Modified chiral triazolium salts for enantioselective benzoin cyclization of enolizable keto-aldehydes: Synthesis of (+)-sappanone B

被引:112
作者
Takikawa, Hiroshi [1 ]
Suzuki, Keisuke [1 ]
机构
[1] Tokyo Inst Technol, SORST JST Agcy, Dept Chem, Meguro Ku, Tokyo 1528551, Japan
关键词
D O I
10.1021/ol070929p
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Asymmetric synthesis of (+)-sappanone B (1), a natural product with a 3-hydroxy chromanone structure, was achieved via enantioselective benzoin cyclization by using a modified Rovis catalyst and triethylamine. This catalyst enabled the successful benzoin cyclization of readily enolizable keto-aldehydes.
引用
收藏
页码:2713 / 2716
页数:4
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