Synthesis of 3-hetarylpyrroles by Suzuki–Miyaura cross-coupling

dc.contributor.authorMatyugina, Elena S.
dc.contributor.authorKhandazhinskaya, Anastasia L.
dc.contributor.authorKochetkov, Sergey N.
dc.contributor.authorSeley-Radtke, Katherine
dc.date.accessioned2025-07-30T19:22:36Z
dc.date.issued2020-05-21
dc.description.abstract1-[tert-Butyl(diphenyl)silyl]pyrrol-3-ylboronic acid was obtained from pyrrole in three steps. Its Suzuki–Miyaura cross-coupling with functionalized pyridinyl and pyrimidinyl bromides afforded new promising 3-hetaryl-1H-pyrroles.
dc.description.sponsorshipThis work was supported by the Russian Science Foundation (project no. 19-74-10048)
dc.description.urihttps://pmc.ncbi.nlm.nih.gov/articles/PMC7241993/
dc.format.extent2 pages
dc.genrejournal articles
dc.identifierdoi:10.13016/m2yfyq-zgrv
dc.identifier.citationMatyugina, Elena S., Anastasia L. Khandazhinskaya, Sergey N. Kochetkov, and Katherine L. Seley-Radtke. “Synthesis of 3-Hetarylpyrroles by Suzuki–Miyaura Cross-Coupling.” Mendeleev Communications 30, no. 2 (March 1, 2020): 231–32. https://doi.org/10.1016/j.mencom.2020.03.034.
dc.identifier.urihttps://doi.org/10.1016/j.mencom.2020.03.034
dc.identifier.urihttp://hdl.handle.net/11603/39571
dc.language.isoen_US
dc.publisherElsevier
dc.relation.isAvailableAtThe University of Maryland, Baltimore County (UMBC)
dc.relation.ispartofUMBC Faculty Collection
dc.relation.ispartofUMBC Chemistry & Biochemistry Department
dc.rightsThis item is likely protected under Title 17 of the U.S. Copyright Law. Unless on a Creative Commons license, for uses protected by Copyright Law, contact the copyright holder or the author.
dc.subjectpyrrole
dc.subjectSuzuki–Miyaura cross-coupling
dc.subjectsilyl protection
dc.subjectfleximers
dc.subjectheterocyclic aromatic compounds
dc.subjectiodination
dc.titleSynthesis of 3-hetarylpyrroles by Suzuki–Miyaura cross-coupling
dc.typeText
dcterms.creatorhttps://orcid.org/0000-0002-0154-3459

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