Synthesis of bis(pyrrol-2-yl)arenes by Pd-catalyzed cross coupling

dc.contributor.author Setsune, Jun ichiro
dc.contributor.author Toda, Masayuki
dc.contributor.author Watanabe, Keigo
dc.contributor.author Panda, Pradeepta K.
dc.contributor.author Yoshida, Takafumi
dc.date.accessioned 2022-03-27T08:38:35Z
dc.date.available 2022-03-27T08:38:35Z
dc.date.issued 2006-10-23
dc.description.abstract 2-Borylpyrrole was prepared from 2-iodopyrrole almost quantitatively and then reacted with dihaloarenes under typical reaction conditions of Suzuki-Miyaura cross coupling to give bis(pyrrol-2-yl)arenes in good yields, while the cross coupling reaction of 2-iodopyrrole with 1,4-phenylenebisboronic acid was susceptible to oxidative self-coupling to produce 4,4′-bis(pyrrol-2-yl)biphenyl as a byproduct. These bis(pyrrol-2-yl)arenes showed strong fluorescence. © 2006 Elsevier Ltd. All rights reserved.
dc.identifier.citation Tetrahedron Letters. v.47(43)
dc.identifier.issn 00404039
dc.identifier.uri 10.1016/j.tetlet.2006.08.098
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0040403906017175
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11335
dc.title Synthesis of bis(pyrrol-2-yl)arenes by Pd-catalyzed cross coupling
dc.type Journal. Article
dspace.entity.type
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