钯催化Suzuki-Miyaura偶联反应合成联苯肼衍生物及生物学评价

M. Chauhan, N. Solanki
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引用次数: 0

摘要

一般报道了几种构建联苯的方法,包括Stille偶联、GombergBachmann反应、Ullmann反应和Suzuki-Miyaura交叉偶联。在本研究中,考虑到这些方法的特殊性和目标化合物的特点,通过Suzuki-Miyaura交叉偶联反应。以1-溴-4-碘苯和苯硼酸为原料,在不同条件下进行了模型反应。产物经FT-IR、质谱、1H NMR和13C NMR表征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and Biological Evaluation of Biphenyl Derivatives of Hydrazine via Palladium Catalyzed Suzuki-Miyaura Coupling Reaction
Generally, several methods for the construction of biphenyls, including Stille coupling, GombergBachmann reaction, Ullmann reaction and Suzuki-Miyaura cross-coupling are reported. In present research, considering the particularities of these methods and the characteristics of the target compounds by Suzuki-Miyaura cross-coupling reaction. To investigate the optimal conditions, a model reaction was performed using 1-bromo-4-iodobenzene and phenyl boronic acid under different conditions. The products were characterized by FT-IR, mass, 1H NMR and 13C NMR spectroscopy.
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