An efficient access to both enantiomers of pipecolic acid

被引：1
|
作者：
Watanabe, LA
Haranaka, S
Jose, B
Yoshida, M
Kato, T
Moriguchi, M
Soda, K
Nishino, N [1 ]
机构：
[1] Kyushu Inst Technol, Grad Sch Life Sci & Syst Engn, Kitakyushu, Fukuoka 8080196, Japan
[2] Kyushu Inst Technol, Fac Engn, Kitakyushu, Fukuoka 8048550, Japan
[3] Japan Sci & Technol Agcy, CREST, Res Project, Saitama 332001, Japan
[4] RIKEN, Saitama 3510198, Japan
[5] Oita Univ, Fac Engn, Oita 8701192, Japan
[6] Kansai Univ, Fac Engn, Suita, Osaka 5648680, Japan
来源：
TETRAHEDRON-ASYMMETRY | 2005年 / 16卷 / 04期
关键词：
D O I：
暂无
中图分类号：
O61 [无机化学];
学科分类号：
070301 ; 081704 ;
摘要：
An efficient and convenient synthesis of both enantiomers of pipecolic acid has been developed using the intramolecular cyclization of 2-amino-6-bromohexanoic acid under mild conditions. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码：903 / 908
页数：6
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