Key Laboratory of Medicinal Chemistry for Natural Resource (Yunnan University), Ministry of Education, School of Chemical Science and Technology , Yunnan University , Kunming 650091 , People's Republic of China.
J Org Chem. 2019 Feb 15;84(4):1797-1807. doi: 10.1021/acs.joc.8b02594. Epub 2019 Jan 31.
A new strategy for the construction of two kinds of fully substituted pyrroles, including 2-aminopyrroles and bicyclic pyrroles from Morita-Baylis-Hillman (MBH) acetates with 1,1-enediamines (EDAMs), or heterocyclic ketene aminals (HKAs) via base-promoted tandem Michael addition, elimination, and aromatization sequence has been developed, affording the expected products in moderate to excellent yields. This methodology is a highly efficient, concise way to access 2-aminopyrroles or bicyclic pyrroles with diversity in molecular structures from accessible building blocks under moderate reaction conditions.
一种新的策略,用于构建两种完全取代的吡咯,包括 2-氨基吡咯和双环吡咯,由 Morita-Baylis-Hillman (MBH) 乙酸盐与 1,1-二胺(EDAMs)或杂环烯酮亚胺(HKAs)通过碱促进的串联迈克尔加成、消除和芳构化序列合成,以中等至优异的产率得到预期产物。该方法是一种高效、简洁的方法,可在温和的反应条件下,从易得的构建块中获得具有多样性分子结构的 2-氨基吡咯或双环吡咯。