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

页码：903 / 908

页数：6

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