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A One-Pot Radio-synthesis of [18 F]PARPi
Journal of Labelled Compounds and Radiopharmaceuticals ( IF 1.8 ) Pub Date : 2020-06-16 , DOI: 10.1002/jlcr.3847
Thomas C Wilson 1 , Nagavarakishore Pillarsetty 1, 2 , Thomas Reiner 1, 2, 3
Affiliation  

In this paper, we disclose a new strategy for the radio-synthesis of [18 F]PARPi from the corresponding, boc-protected, nitro-precursor. Using a two-step procedure, [18 F]PARPi could be isolated in radiochemical yields up to 9.6%. The reaction proceeds via an efficient one-pot, two-step process, allowing for simplification over previous methods that require complex multi-step, multi-pot strategies to be implemented.

中文翻译:

[18 F]PARPi 的一锅式无线电合成

在本文中,我们公开了一种从相应的受 boc 保护的硝基前体放射合成 [18 F]PARPi 的新策略。使用两步程序,[ 18 F]PARPi 可以以高达 9.6% 的放射化学产率分离。该反应通过高效的一锅两步过程进行,从而简化了需要实施复杂的多步、多锅策略的先前方法。
更新日期:2020-06-16
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