ORGN 601-Diastereoselective synthesis of functionalized (Z)-fluoroalkene dipeptide isosteres: Lys-Lys and Glu-Glu type FADIs

被引：0

|

作者：

Narumi, Tetsuo ^{[1
]}

Kodera, Yasuyo ^{[1
]}

Tomita, Kenji ^{[1
]}

Inokuchi, Eriko ^{[1
]}

Oishi, Shinya ^{[1
]}

Ohno, Hiroaki ^{[1
]}

Fujii, Nobutaka ^{[1
]}

机构：

[1] Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan

来源：

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 2007年 / 234卷

关键词：

D O I：

暂无

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

601-ORGN

引用

收藏

页数：1

相关论文

共 2 条

[1] SmI2-mediated reduction of γ,γ-difluoro-α,β-enoates with application to the synthesis of functionalized (Z)-fluoroalkene-type dipeptide isosteres
Otaka, A
Watanabe, J
Yukimasa, A
Sasaki, Y
Watanabe, H
Kinoshita, T
Oishi, S
Tamamura, H
Fujii, N
JOURNAL OF ORGANIC CHEMISTRY, 2004, 69 (05): : 1634 - 1645
[2] A novel one-pot reaction involving organocopper-mediated reduction/transmetalation/asymmetric alkylation, leading to the diastereoselective synthesis of functionalized (Z)-fluoroalkene dipeptide isosteres
Narumi, Tetsuo
Niida, Ayumu
Tomita, Kenji
Oishi, Shinya
Otaka, Akira
Ohno, Hiroaki
Fujii, Nobutaka
CHEMICAL COMMUNICATIONS, 2006, (45) : 4720 - 4722