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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/2988
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dc.contributor.authorSarkar, Bibhas R.-
dc.date.accessioned2021-10-27T04:13:37Z-
dc.date.available2021-10-27T04:13:37Z-
dc.date.issued2018-03-
dc.identifier.urihttps://www.tandfonline.com/doi/full/10.1080/00397911.2018.1428347-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2988-
dc.description.abstractEfficient Mizoroki–Heck couplings were obtained using a very easily synthesizable palladium(II) complex of hemilabile N–O ligand (picolinate), with high turnover frequencies up to >10,000 h−1, in just 15 min, with high selectivity of >99% to the desired products. Wide applicability of the simple-looking palladium complex catalyst was established with differently functionalized substrates. Catalyst screening studies revealed intricate details of dependence of catalyst performance on different reaction parameters and conditions and arriving at the optimized facile methodology.en_US
dc.language.isoenen_US
dc.publisherTaylor & Francisen_US
dc.subjectChemistryen_US
dc.subjectHeck couplingen_US
dc.subjectHemilabile N–O liganden_US
dc.subjectHomogeneous catalystsen_US
dc.subjectPd(II)-complexen_US
dc.titleEfficient Mizoroki–Heck coupling reactions using phosphine-modified Pd(II)–picolinate complexen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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