Departamento de Química, CCE, Universidade Federal de Viçosa , Viçosa, MG 36570-900, Brazil.
Departamento de Química, ICEx, Universidade Federal de Minas Gerais , Belo Horizonte, MG 31270-901, Brazil.
J Org Chem. 2018 Feb 16;83(4):1761-1771. doi: 10.1021/acs.joc.7b02532. Epub 2018 Feb 2.
A new one-pot cascade reaction-based application of Povarov reactions with a p-sulfonic acid calix[4]arene catalyst for the synthesis of a series of 34 julolidine derivatives with substituents at C8 or C9 in good to excellent yields is reported. These microwave-assisted reactions proceeded efficiently, had short reaction times, were metal-free, were low cost, and used an inexpensive, easily available and nontoxic catalyst. These advantages, along with a simple workup procedure, make this protocol a very efficient and green alternative to the traditional methods for constructing these types of N-heterocyclic skeletons. In addition, this protocol allows the formation of julolidine structures, which requires the construction of four new C-C bonds and two C-N bonds. A mechanism for the Povarov reaction involving a stepwise sequence via ionic intermediates was proposed and validated.
一种新的基于 Povarov 反应的一锅级联反应应用,使用对磺酸杯[4]芳烃催化剂,用于合成一系列在 C8 或 C9 位带有取代基的 34 个 julolidine 衍生物,产率良好至优秀。这些微波辅助反应效率高,反应时间短,无金属,成本低,使用廉价、易得且无毒的催化剂。这些优点,再加上简单的后处理步骤,使得该方法成为传统方法的一种非常有效和绿色的替代方法,用于构建这些类型的 N-杂环骨架。此外,该方法允许 julolidine 结构的形成,这需要构建四个新的 C-C 键和两个 C-N 键。提出并验证了涉及离子中间体分步序列的 Povarov 反应机理。