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dc.contributor.authorDuan, Shaofeng
dc.contributor.authorJana, Ranjan
dc.contributor.authorTunge, Jon A.
dc.date.accessioned2017-04-12T17:56:05Z
dc.date.available2017-04-12T17:56:05Z
dc.date.issued2009-06-19
dc.identifier.citationDuan, S., Jana, R., & Tunge, J. A. (2009). Lewis acid-catalyzed diastereoselective hydroarylation of benzylidene malonic esters. The Journal of Organic Chemistry, 74(12), 4612–4614. http://doi.org/10.1021/jo900367gen_US
dc.identifier.urihttp://hdl.handle.net/1808/23640
dc.description.abstractHerein we report that simple Lewis acids catalyze the hydroarylation of benzylidene malonates with phenols. Ultimately, 3,4-disubstituted dihydrocoumarins are obtained via a hydroarylation-lactonization sequence. Moreover, the dihydrocoumarins are formed with a high degree of diastereoselectivity favoring the trans stereoisomer.en_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in the Journal of Organic Chemistry, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://dx.doi.org/10.1021/jo900367g.en_US
dc.titleLewis acid-catalyzed diastereoselective hydroarylation of benzylidene malonic estersen_US
dc.typeArticleen_US
kusw.kuauthorDuan, Shaofeng
kusw.kuauthorJana, Ranjan
kusw.kuauthorTunge, Jon A.
kusw.kudepartmentChemistryen_US
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dc.identifier.doi10.1021/jo900367gen_US
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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