Organic Reaction Monitoring of a Glycine Derivative Using Signal Amplification by Reversible Exchange-Hyperpolarized Benchtop Nuclear Magnetic Resonance Spectroscopy

被引:25
作者
Chae, Heelim [1 ]
Min, Sein [1 ]
Jeong, Hye Jin [1 ]
Namgoong, Sung Keon [1 ]
Oh, Sangwon [2 ]
Kim, Kiwoong [2 ,3 ]
Jeong, Keunhong [4 ]
机构
[1] Seoul Womens Univ, Dept Chem, South, Seoul 01797, South Korea
[2] Korea Res Inst Stand & Sci, Daejeon 34113, South Korea
[3] Univ Sci & Technol, Deparment Med Phys, Daejeon 34113, South Korea
[4] Korea Mil Acad, Dept Chem, Seoul 01805, South Korea
基金
新加坡国家研究基金会;
关键词
PARAHYDROGEN-INDUCED POLARIZATION; PARA-HYDROGEN; NMR; SABRE; SPIN; ORDER;
D O I
10.1021/acs.analchem.0c01270
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Currently, signal amplification by reversible exchange (SABRE) using para-hydrogen is an attractive method of hyperpolarization for overcoming the sensitivity problems of nuclear magnetic resonance (NMR) spectroscopy. Additionally, SABRE, using the spin order of para-hydrogen, can be applied in reaction monitoring processes for organic chemistry reactions where a small amount of reactant exists. The organic reaction monitoring system created by integrating SABRE and benchtop NMR is the ideal combination for monitoring a reaction and identifying the small amounts of materials in the middle of the reaction. We used a laboratory-built setup, prepared materials by synthesis, and showed that the products obtained by esterification of glycine were also active in SABRE. The products, which were synthesized esterified glycine with nicotinoyl chloride hydrochloride, were observed with a reaction monitoring system. The maximum SABRE enhancement among them (approximately 147-fold) validated the use of this method. This study is the first example of the monitoring of this organic reaction by SABRE and benchtop NMR. It will open new possibilities for applying this system to many other organic reactions and also provide more fruitful future applications such as drug discovery and mechanism study.
引用
收藏
页码:10902 / 10907
页数:6
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