首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Synthesis of (S)-naproxen-benzotriazole and its application as chiral derivatizing reagent for microwave-assisted synthesis and indirect high performance liquid chromatographic separation of diastereomers of penicillamine, cysteine and homocysteine
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Synthesis of (S)-naproxen-benzotriazole and its application as chiral derivatizing reagent for microwave-assisted synthesis and indirect high performance liquid chromatographic separation of diastereomers of penicillamine, cysteine and homocysteine

机译:(S)-萘普生-苯并三唑的合成及其作为手性衍生剂在微波辅助合成和青霉素,半胱氨酸和高半胱氨酸非对映异构体的间接高效液相色谱分离中的应用

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摘要

(S)-Naproxen-benzotriazole was synthesized by the reaction of (S)-naproxen with 1. H-benzotriazole using coupling reagent dicyclohexyl carbodiimide and 4-dimethylamino pyridine (DCC/DMAP). It was used as chiral derivatizing reagent for microwave irradiated synthesis of diastereomers of penicillamine, cysteine and homocysteine. The diastereomers were separated by reversed phase high performance liquid chromatography using gradient elution of triethylammonium phosphate (pH 3.5)-acetonitrile (30-65% within 30 min). The method was validated for accuracy, precision, and limit of detection.
机译:(S)-萘普生-苯并三唑是通过(S)-萘普生与1. H-苯并三唑的反应使用偶合剂二环己基碳二亚胺和4-二甲氨基吡啶(DCC / DMAP)合成的。用作手性衍生试剂,用于微波辐照合成青霉素胺,半胱氨酸和高半胱氨酸的非对映异构体。通过反相高效液相色谱,使用磷酸三乙铵(pH 3.5)-乙腈(30分钟内30-65%)的梯度洗脱,分离非对映异构体。验证了该方法的准确性,准确性和检测极限。

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