化学
范围(计算机科学)
冷凝
有机化学
组合化学
嘌呤代谢
程序设计语言
计算机科学
热力学
物理
酶
作者
Olivier René,Alexandra Souverneva,Steven R. Magnuson,Benjamin P. Fauber
标识
DOI:10.1016/j.tetlet.2012.09.069
摘要
We report an efficient one-step route to 2-fluoroalkylbenzimidazoles and -benzothiazoles via the condensation of fluorinated carboxylic acids and aromatic diamines or aminothiophenols. Additionally, we describe the syntheses of fluoroalkyl-azabenzimidazoles, -purines, and -imidazolopyrazines. This method is high-yielding with broad scope and is operationally simple with potential application to parallel synthesis.
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