Asymmetric synthesis of flindersiachromanone using lipase-catalyzed reaction

被引：8
|
作者：
Kawasaki, M
Yoshikai, H
Kakuda, H
Toyooka, N
Tanaka, A
Goto, M
Kometani, T
机构：
[1] Toyama Prefectural Univ, Dept Liberal Arts & Sci, Fac Engn, Toyama 9390398, Japan
[2] Toyama Prefectural Univ, Dept Bioresources Sci, Coll Technol, Toyama 9390398, Japan
[3] Toyama Univ, Chem Lab, Toyama 9300194, Japan
[4] Toyama Univ, Fac Pharmaceut Sci, Toyama 9300194, Japan
[5] Toyama Natl Coll Technol, Dept Chem & Biochem Engn, Toyama 9398630, Japan
来源：
HETEROCYCLES | 2006年 / 68卷 / 03期
关键词：
D O I：
10.3987/COM-05-10652
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
The (R)- and (S)-enantiomers of flindersiachromanone (2-(2-phenylethyl)-4-chromanone) were synthesized from the enantiomerically pure 1-phenyl-5-hexen-3-ol obtained via the lipase-catalyzed enantioselective transesterification.
引用
收藏
页码：483 / 493
页数：11
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