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dc.contributor.authorBora, Darshana
dc.contributor.authorElza John, Stephy
dc.contributor.authorSravani Galla, Mary
dc.contributor.authorSathish, Manda
dc.contributor.authorShankaraiah, Nagula
dc.date.accessioned2022-12-14T17:25:39Z
dc.date.available2022-12-14T17:25:39Z
dc.date.issued2022
dc.identifier.urihttp://repositorio.ucm.cl/handle/ucm/4213
dc.description.abstractThe rhodium-catalysed ortho-selective carbenes insertion strategy to activate the non-acidic sp2 Csingle bondH bond of β-carboline and isoquinoline scaffolds was developed. This transformation endows facile fabrication of Csingle bondC bond with high atom economy, pleasant yields and wide functional group tolerance exploiting directing properties of pyridinic nitrogen. In this protocol, diazo compounds of diethyl malonate, dimethyl dimedone and oxindole are tested as carbene source with the release of environmentally benign N2 gas as the by-product. Moreover, to perceive mechanistic insights, ESI-MS studies were conducted, and the key intermediates associated with this transformation were identified. In addition, the metal-free construction of planar polycyclic indolizine-indole frameworks has been accomplished from the synthesized products. Furthermore, the neoplastic and fluorescence properties of Csingle bondN annulated compounds were also determined.es_CL
dc.language.isoenes_CL
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 Chile*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
dc.sourceMolecular Catalysis, 533, 112783es_CL
dc.subjectRh(III)-catalystes_CL
dc.subjectC-H activationes_CL
dc.subjectCarbenees_CL
dc.subjectAlkylationes_CL
dc.subjectC-N bond annulationes_CL
dc.titleRh(III)-catalysed site-selective alkylation of β-carbolines/isoquinolines and tandem Csingle bondH/Csingle bondN functionalization to construct indolizine-indole frameworkses_CL
dc.typeArticlees_CL
dc.ucm.indexacionScopuses_CL
dc.ucm.indexacionIsies_CL
dc.ucm.urisciencedirect.com/science/article/abs/pii/S2468823122006691?via%3Dihubes_CL
dc.ucm.doidoi.org/10.1016/j.mcat.2022.112783es_CL


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Atribución-NoComercial-SinDerivadas 3.0 Chile
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