Synthesis of stereochemically defined (E)-cinnamyl alcohol derivatives from the Baylis-Hillman adducts

被引：0
|
作者：
Kim, HS [1 ]
Kim, TY [1 ]
Lee, KY [1 ]
Chung, YM [1 ]
Lee, HJ [1 ]
Kim, JN [1 ]
机构：
[1] Chonnam Natl Univ, Dept Chem, Kwangju 500757, South Korea
来源：
TETRAHEDRON LETTERS | 2000年 / 41卷 / 15期
关键词：
allylic alcohols; Baylis-Hillman adducts; trifluoroacetic acid;
D O I：
暂无
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
The reaction of the Baylis-Hillman adducts 1a-g and trifluoroacetic acid at 30-70 degrees C gave the rearranged cinnamyl alcohols 2a-g stereoselectively in moderate yields. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码：2613 / 2616
页数：4
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