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Metal-free transannulation reaction of indoles with nitrostyrenes: a simple practical synthesis of 3-substituted 2-quinolones

dc.contributor.authorAksenov, Alexander V.
dc.contributor.authorSmirnov, Alexander N.
dc.contributor.authorAksenov, Nicolai A.
dc.contributor.authorAksenova, Inna V.
dc.contributor.authorFrolova, Liliya V.
dc.contributor.authorKornienko, Alexander
dc.contributor.authorMagedov, Igor V.
dc.contributor.authorRubin, Michael
dc.date.accessioned2017-02-22T20:56:56Z
dc.date.available2017-02-22T20:56:56Z
dc.date.issued2016-07-15
dc.identifier.citationAksenov, Alexander V., Alexander N. Smirnov, Nicolai A. Aksenov, Inna V. Aksenova, Liliya V. Frolova, Alexander Kornienko, Igor V. Magedov, and Michael Rubin. "Metal-free Transannulation Reaction of Indoles with Nitrostyrenes: A Simple Practical Synthesis of 3-substituted 2-quinolones." Chemical Communications 49.81 (2013): 9305.en_US
dc.identifier.urihttp://hdl.handle.net/1808/23223
dc.description.abstract3-Substituted 2-quinolones are obtained via a novel, metal-free transannulation reaction of 2-substituted indoles with 2-nitroalkenes in polyphosphoric acid. The reaction can be used in conjunction with the Fisher indole synthesis offering a practical three-component heteroannulation methodology to produce 2-quinolones from arylhydrazines, 2-nitroalkenes and acetophenone.en_US
dc.publisherRoyal Society of Chemistryen_US
dc.titleMetal-free transannulation reaction of indoles with nitrostyrenes: a simple practical synthesis of 3-substituted 2-quinolonesen_US
dc.typeArticleen_US
kusw.kuauthorRubin, Michael
kusw.kudepartmentChemistryen_US
dc.identifier.doi10.1039/c3cc45696jen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-1668-9311
kusw.oaversionScholarly/refereed, author accepted manuscripten_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.rights.accessrightsopenAccess


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