| dc.contributor.author | Grenning, Alexander J. | |
| dc.contributor.author | Tunge, Jon A. | |
| dc.date.accessioned | 2017-04-06T18:42:46Z | |
| dc.date.available | 2017-04-06T18:42:46Z | |
| dc.date.issued | 2011-02-11 | |
| dc.identifier.citation | Grenning, A. J., & Tunge, J. A. (2011). Deacylative allylation of nitroalkanes: unsymmetric bisallylation via 3-component coupling. Angewandte Chemie (International Ed. in English), 50(7), 1688–1691. http://doi.org/10.1002/anie.201006273 | en_US |
| dc.identifier.uri | http://hdl.handle.net/1808/23599 | |
| dc.description.abstract | Use it and lose it! Allylic alcohols were used directly for the synthesis of diallylated nitroalkanes in a three-component coupling based on the strategy of deacylative allylation for the in situ generation of a nucleophile and an allyl electrophile (see scheme). | en_US |
| dc.publisher | Wiley | en_US |
| dc.rights | Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim | en_US |
| dc.subject | Deacylation | en_US |
| dc.subject | Tsuji-Trost reaction | en_US |
| dc.subject | Nitroalkane allylation | en_US |
| dc.subject | 1, 6-diene synthesis | en_US |
| dc.title | Deacylative allylation of nitroalkanes: unsymmetric bisallylation via 3-component coupling | en_US |
| dc.type | Article | en_US |
| kusw.kuauthor | Grenning, Alexander James | |
| kusw.kuauthor | Tunge, Jon A. | |
| kusw.kudepartment | Chemistry | en_US |
| dc.identifier.doi | 10.1002/anie.201006273 | 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 | |
