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Facile Buchwald-Hartwig coupling of sterically encumbered substrates effected by PNP ligands

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dc.contributor.author KATHEWAD, NEHA en_US
dc.contributor.author ANAGHA, M. C. en_US
dc.contributor.author PARVIN, NASRINA en_US
dc.contributor.author Parambath, Sneha en_US
dc.contributor.author Parameswaran, Pattiyil en_US
dc.contributor.author KHAN, SHABANA en_US
dc.date.accessioned 2019-03-26T10:01:03Z
dc.date.available 2019-03-26T10:01:03Z
dc.date.issued 2019-01 en_US
dc.identifier.citation Dalton Transactions, 48(8), 2730-2734. en_US
dc.identifier.issn 1477-9226 en_US
dc.identifier.issn 1477-9234 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2380
dc.identifier.uri https://doi.org/10.1039/c9dt00159j en_US
dc.description.abstract The diphosphinoamine ligands [(Ph2P)2N(Ar); 1 (Ar = C6H5), 2 (Ar = 2,6-iPr2C6H3)] were effectively utilized in Buchwald–Hartwig coupling of a range of sterically demanding substrates. The reaction was carried out using conventional and microwave routes and the latter reduces the reaction time from 3 d to 15–30 min. A broad substrate scope was achieved in this protocol and most of the coupling products are isolated on a mutligram scale. DFT calculations were carried out to elucidate the reaction mechanism. en_US
dc.language.iso en en_US
dc.publisher Royal Society of Chemistry en_US
dc.subject Palladium-catalyzed amination en_US
dc.subject Aryl halides en_US
dc.subject C-N en_US
dc.subject Scalable synthesis en_US
dc.subject Carbon en_US
dc.subject Bromides en_US
dc.subject Efficient en_US
dc.subject Arylamines en_US
dc.subject Phosphines en_US
dc.subject Complexes en_US
dc.subject TOC-MAR-2019 en_US
dc.subject 2019 en_US
dc.title Facile Buchwald-Hartwig coupling of sterically encumbered substrates effected by PNP ligands en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Dalton Transactions en_US
dc.publication.originofpublisher Foreign en_US


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