Photoinduced Ring Opening of Methyl 1-Aryl-5-oxo-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazole-2-carboxylates in the Presence of Diaryl Disulfides

IF 0.6 Q4 CHEMISTRY, ORGANIC
Molbank Pub Date : 2023-06-15 DOI:10.3390/m1670
Nejc Petek, Uroš Grošelj
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引用次数: 0

Abstract

Among the methods used for the synthesis of functionalized heterocyclic compounds, photochemistry has gained immense popularity due to the reactivity of intermediates in photoinduced reactions. In this study, we report on the effect of diaryl disulfides as hydrogen atom transfer catalysts on the photoinduced transformations of pyrazolo[1,2-a]pyrazolones. After excitation with visible light, these compounds are susceptible to C–N bond cleavage, followed by intermolecular hydrogen atom abstraction. By modifying the reaction conditions, we have developed two novel methods for the synthesis of highly substituted pyrazoles.
二芳基二硫化物存在下1-芳基-5-氧-6,7-二氢- 1h, 5h -吡唑[1,2-a]吡唑-2-羧酸甲酯的光诱导开环
在用于合成功能化杂环化合物的方法中,光化学由于中间体在光诱导反应中的反应性而获得了极大的普及。在本研究中,我们报道了二芳基二硫化物作为氢原子转移催化剂对吡唑啉[1,2-a]吡唑啉酮光诱导转化的影响。在可见光激发后,这些化合物易发生C-N键断裂,随后发生分子间氢原子抽离。通过改变反应条件,我们开发了两种合成高取代吡唑的新方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molbank
Molbank Chemistry-Physical and Theoretical Chemistry
CiteScore
0.70
自引率
33.30%
发文量
174
审稿时长
11 weeks
期刊介绍: •organic synthesis •biosynthesis •extraction and purification •natural product derivatives •structural elucidation (X-ray crystallography, NMR, etc.)
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