Palladium catalysed sequential imine arylation/Suzuki–Miyaura coupling: synthesis of a-(biarylyl)benzylamines

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dc.contributor.authorMarques, Carolina S.
dc.contributor.authorLocati, Abel
dc.contributor.authorPrates Ramalho, J.P.
dc.contributor.authorBurke, Anthony J.
dc.date.accessioned2016-01-27T16:54:12Z
dc.date.available2016-01-27T16:54:12Z
dc.date.issued2015
dc.date.updated2016-01-20T10:43:00Z
dc.description.abstractreport an innovative, high yielding one-pot sequential catalytic imine arylation/SuzukieMiyaura cross-coupling reaction, which converts suitably activated imine substrates to various biarylarylmethyl amine products using several commercial Pd catalysts. Many biarylarylmethyl amine molecules are biologically active. Insightful computational studies detail the mechanism of the imine arylation process. The sequence of reactions is likely to be dependent on the reaction conditions.por
dc.identifier00404020en_US
dc.identifier.authoremailnd
dc.identifier.authoremailnd
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dc.identifier.citationMarques, Carolina S.; Locati, Abel; Prates Ramalho, J.P.; Burke, Anthony J.Palladium catalysed sequential imine arylation/Suzuki–Miyaura coupling: synthesis of a-(biarylyl)benzylamines, Tetrahedron, 71, 21, 3314-3324, 2015.por
dc.identifier.urihttp://hdl.handle.net/10174/16941
dc.language.isoporpor
dc.rightsrestrictedAccesspor
dc.titlePalladium catalysed sequential imine arylation/Suzuki–Miyaura coupling: synthesis of a-(biarylyl)benzylaminespor
dc.typearticlepor

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