| dc.contributor.author | Duan, Shaofeng | |
| dc.contributor.author | Jana, Ranjan | |
| dc.contributor.author | Tunge, Jon A. | |
| dc.date.accessioned | 2017-04-12T17:56:05Z | |
| dc.date.available | 2017-04-12T17:56:05Z | |
| dc.date.issued | 2009-06-19 | |
| dc.identifier.citation | Duan, 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/jo900367g | en_US |
| dc.identifier.uri | http://hdl.handle.net/1808/23640 | |
| dc.description.abstract | Herein 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.publisher | American Chemical Society | en_US |
| dc.rights | This 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.title | Lewis acid-catalyzed diastereoselective hydroarylation of benzylidene malonic esters | en_US |
| dc.type | Article | en_US |
| kusw.kuauthor | Duan, Shaofeng | |
| kusw.kuauthor | Jana, Ranjan | |
| kusw.kuauthor | Tunge, Jon A. | |
| kusw.kudepartment | Chemistry | en_US |
| dc.identifier.doi | 10.1021/jo900367g | en_US |
| 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 | |
