Catalyst‐Controlled Regioselective Approach to 1‐Aminoisoquinolines and/or 1‐Aminoisoindolines through Aminative Domino Cycliza­tion of 2‐Alkynylbenzonitriles

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dc.contributor.authorReddy, V.
dc.contributor.authorJadhav, A.S.
dc.contributor.authorAnand, R.V.
dc.date.accessioned2020-12-03T05:01:36Z
dc.date.available2020-12-03T05:01:36Z
dc.date.issued2016
dc.description.abstractMetal‐controlled domino reaction: A metal catalyzed regioselective aminative domino cyclization of 2‐alkynylbenzonitriles leading to 1‐aminoisoquinolines and/or 1‐aminoisoindolines was developed under solvent‐free conditions. It was found that the regioselectivity of the reaction was greatly influenced by the choice of metal catalyst.en_US
dc.identifier.citationEuropean Journal of Organic Chemistry, 2016(3), pp. 453-458en_US
dc.identifier.otherhttps://doi.org/10.1002/ejoc.201501390
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.201501390
dc.identifier.urihttp://hdl.handle.net/123456789/2541
dc.language.isoenen_US
dc.publisherWiley-VCH Verlagen_US
dc.subjectAminationen_US
dc.subjectHeterocyclesen_US
dc.subjectIsoquinolinesen_US
dc.subjectIsoindolinesen_US
dc.subjectDomino reactionsen_US
dc.titleCatalyst‐Controlled Regioselective Approach to 1‐Aminoisoquinolines and/or 1‐Aminoisoindolines through Aminative Domino Cycliza­tion of 2‐Alkynylbenzonitrilesen_US
dc.typeArticleen_US

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