Synthesis and Conformational Analysis of Fluorine-Containing Oligopeptides

被引：0
|
作者：
Yamazaki, Takashi [1 ]
Kitamoto, Takamasa [1 ]
Marubayashi, Shunsuke [1 ]
机构：
[1] Tokyo Univ Agr & Technol, Inst Symbiot Sci & Technol, Strateg Res Initiat Future Nanosci & Technol, Koganei, Tokyo 1848588, Japan
来源：
CURRENT FLUOROORGANIC CHEMISTRY: NEW SYNTHETIC DIRECTIONS, TECHNOLOGIES, MATERIALS, AND BIOLOGICAL APPLICATIONS | 2007年 / 949卷
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D O I：
暂无
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
Preparation of hexapeptide Tyr-D-Ser-Gly-Phe-Leu-Thr possessing an interesting g-selective opioid activity as well as its F(3)-analog at the Thr terminal methyl group was carried out to investigate the effect of highly electronegative fluorine atoms toward the conformation of the molecules on the basis of information obtained from various types of (1)H NMR techniques.
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页码：409 / 419
页数：11
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