School of Science and Technology, Chemistry Division, University of Camerino, Via S. Agostino n. 1, 62032 Camerino (MC), Italy.
Org Biomol Chem. 2020 Jun 24;18(24):4533-4546. doi: 10.1039/d0ob00956c.
Functionalization of pyrroles introducing a 2-nitroalkyl moiety allows the formation of nitro-containing compounds to be used as pivotal intermediates for the synthesis of bioactive compounds. The reaction of pyrroles with nitroalkenes under the Friedel-Crafts conditions allows a direct entry to 2-(2-nitroalkyl)pyrroles. This approach can also be used for the preparation of enantioenriched derivatives exploiting asymmetric catalysis. In a complementary fashion, the Henry reaction between 2-formylpyrroles and nitroalkanes generates the corresponding nitroaldol products which upon dehydration and reduction of the intermediate 2-pyrrolylnitroethene efficiently afford 2-(2-nitroalkyl)pyrroles. This review article summarizes the most relevant procedures for the preparation of 2-(2-nitroalkyl)pyrroles during the last two decades as well as their significant practical applications.
功能化吡咯,引入 2-硝烷基部分,可使含硝基的化合物作为生物活性化合物合成的关键中间体。在 Friedel-Crafts 条件下,吡咯与硝基烯烃反应可以直接得到 2-(2-硝烷基)吡咯。这种方法也可以用于通过不对称催化制备对映体富集的衍生物。以互补的方式,2-甲酰基吡咯与硝基烷烃之间的 Henry 反应生成相应的硝基醇醛产物,这些产物经中间 2-吡咯基硝基乙烯脱水和还原,有效地得到 2-(2-硝烷基)吡咯。本文综述了过去二十年中制备 2-(2-硝烷基)吡咯的最相关方法及其重要的实际应用。