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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >SIMPLE AND STEREOCONTROLLED PREPARATION OF BENZOYLATED PHENYLALANINE USING FRIEDEL-CRAFTS REACTION IN TRIFLUOROMETHANESULFONIC ACID FOR PHOTO AFFINITY LABELING
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SIMPLE AND STEREOCONTROLLED PREPARATION OF BENZOYLATED PHENYLALANINE USING FRIEDEL-CRAFTS REACTION IN TRIFLUOROMETHANESULFONIC ACID FOR PHOTO AFFINITY LABELING

机译:三氟甲磺酸中弗利德尔-克拉夫特反应的简单和立体控制制备光亲和性标签中的苯并丙氨酸

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摘要

-Simple and stereocontrolled preparation of benzoylated phenylalanine derivatives from optically pure phenylalanine using Friedel-Crafts reaction in trifluoromethanesulfonic acid (TfOH) is reported; these derivatives are useful for photoaffinity labeling. Protected or unprotected phenylalanine derivatives were converted to benzoyl derivatives in TfOH at room temperature in a short time without loss of optical purity. The reaction condition was applied to synthesize novel photoreactive phenylalanine derivative, which has two photophores (benzophenone and diazirine). The detail analysis of photo-irradiation for two different photophores contained phenylalanine derivative was also investigated.
机译:-报道了在三氟甲磺酸(TfOH)中使用Friedel-Crafts反应从光学纯的苯丙氨酸简单而立体控制地制备苯甲酰化的苯丙氨酸衍生物;这些衍生物可用于光亲和标记。在室温下,在短时间内在TfOH中将受保护或未保护的苯丙氨酸衍生物转化为苯甲酰基衍生物,而不会损失光学纯度。以反应条件为基础,合成了具有两个光团(二苯甲酮和二嗪)的新型光反应性苯丙氨酸衍生物。还研究了两种不同的含有苯丙氨酸衍生物的荧光粉的光辐照的详细分析。

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