One-pot synthesis of benzotripyrrole derivatives from 1: H -pyrroles

dc.contributor.author Pandeeti, Obaiah
dc.contributor.author Bijigiri, Sathish Kumar
dc.contributor.author Panda, Pradeepta K.
dc.date.accessioned 2022-03-27T08:37:50Z
dc.date.available 2022-03-27T08:37:50Z
dc.date.issued 2019-01-01
dc.description.abstract Herein, we report, for the first time, the synthesis of C3h symmetric benzotripyrroles having unprotected pyrrolic nitrogens in a single step from a known starting material, i.e. 2-methyl-1H-pyrrole-3-carboxylates, and characterized the isolated intermediate compounds to elucidate the mechanism. Further, computational studies were performed to probe the dual descriptor and aromaticity to understand the reactivity of the pyrrole derivatives towards cyclization and the stability of the benzotripyrrole.
dc.identifier.citation New Journal of Chemistry. v.43(47)
dc.identifier.issn 11440546
dc.identifier.uri 10.1039/c9nj04700j
dc.identifier.uri http://xlink.rsc.org/?DOI=C9NJ04700J
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11283
dc.title One-pot synthesis of benzotripyrrole derivatives from 1: H -pyrroles
dc.type Journal. Article
dspace.entity.type
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