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dc.contributor.authorDuan, Shaofeng
dc.contributor.authorJana, Ranjan
dc.contributor.authorTunge, Jon A.
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.
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
dc.titleLewis acid-catalyzed diastereoselective hydroarylation of benzylidene malonic estersen_US
kusw.kuauthorDuan, Shaofeng
kusw.kuauthorJana, Ranjan
kusw.kuauthorTunge, Jon A.
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kusw.oaversionScholarly/refereed, author accepted manuscripten_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US

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