dc.contributor.author | Aksenov, Alexander V. | |
dc.contributor.author | Smirnov, Alexander N. | |
dc.contributor.author | Aksenov, Nicolai A. | |
dc.contributor.author | Aksenova, Inna V. | |
dc.contributor.author | Frolova, Liliya V. | |
dc.contributor.author | Kornienko, Alexander | |
dc.contributor.author | Magedov, Igor V. | |
dc.contributor.author | Rubin, Michael | |
dc.date.accessioned | 2017-02-22T20:56:56Z | |
dc.date.available | 2017-02-22T20:56:56Z | |
dc.date.issued | 2016-07-15 | |
dc.identifier.citation | Aksenov, 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.uri | http://hdl.handle.net/1808/23223 | |
dc.description.abstract | 3-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.publisher | Royal Society of Chemistry | en_US |
dc.title | Metal-free transannulation reaction of indoles with nitrostyrenes: a simple practical synthesis of 3-substituted 2-quinolones | en_US |
dc.type | Article | en_US |
kusw.kuauthor | Rubin, Michael | |
kusw.kudepartment | Chemistry | en_US |
dc.identifier.doi | 10.1039/c3cc45696j | en_US |
dc.identifier.orcid | https://orcid.org/0000-0002-1668-9311 | |
kusw.oaversion | Scholarly/refereed, author accepted manuscript | en_US |
kusw.oapolicy | This item meets KU Open Access policy criteria. | en_US |
dc.rights.accessrights | openAccess | |